Skip to main content

The effect of a multidisciplinary lifestyle program for patients with rheumatoid arthritis, an increased risk for rheumatoid arthritis or with metabolic syndrome-associated osteoarthritis: the “Plants for Joints” randomized controlled trial protocol


Low-grade inflammation and metabolic syndrome are seen in many chronic diseases, including rheumatoid arthritis (RA) and osteoarthritis (OA). Lifestyle interventions which combine different non-pharmacological therapies have shown synergizing effects in improving outcomes in patients with other chronic diseases or increased risk thereof, especially cardiovascular disease. For RA and metabolic syndrome-associated OA (MSOA), whole food plant-based diets (WFPDs) have shown promising results. A WFPD, however, had not yet been combined with other lifestyle interventions for RA and OA patients. In this protocol paper, we therefore present Plants for Joints, a multidisciplinary lifestyle program, based on a WFPD, exercise, and stress management. The objective is to study the effect of this program on disease activity in patients with RA (randomized controlled trial [RCT] 1), on a risk score for developing RA in patients with anti-citrullinated protein antibody (ACPA) positive arthralgia (RCT 2) and on pain, stiffness, and function in patients with MSOA (RCT 3), all in comparison with usual care.

We designed three 16-week observer-blind RCTs with a waiting-list control group for patients with RA with low to moderate disease activity (2.6 ≤ Disease Activity Score [DAS28] ≤ 5.1, RCT 1, n = 80), for patients at risk for RA, defined by ACPA-positive arthralgia (RCT 2, n = 16) and for patients with metabolic syndrome and OA in the knee and/or hip (RCT 3, n = 80). After personal counseling on diet and exercise, participants join 10 group meetings with 6–12 other patients to receive theoretical and practical training on a WFPD, exercise, and stress management, while medication remains unchanged. The waiting-list control group receives usual care, while entering the program after the RCT. Primary outcomes are: difference in mean change between intervention and control groups within 16 weeks for the DAS28 in RA patients (RCT 1), the RA-risk score for ACPA positive arthralgia patients (RCT 2), and the Western Ontario and McMaster Universities Arthritis Index (WOMAC) score for MSOA patients (RCT 3). Continued adherence to the lifestyle program is measured in a two-year observational extension study.

Peer Review reports


The development of rheumatoid arthritis (RA) and osteoarthritis (OA) have been linked to diet and obesity [1,2,3,4,5,6,7,8]. Studies indicate fasting, a Mediterranean diet, as well as a whole food plant-based diet (WFPD) can lower disease activity in patients with RA [9,10,11,12,13,14]. In OA, hypocaloric and WFPDs showed favorable results, while the effect of a hypocaloric diet in combination with exercise was superior, suggesting synergies for multidisciplinary interventions [15,16,17,18].

For exercise, it has been shown that physical activity is associated with a lower risk of RA [19]. In patients with RA, long-term high-intensity exercise is effective in improving functional and emotional status [20]. Routinely combining aerobic exercise with muscle strength training (similar to the Dutch Exercise Guideline) is recommended for patients with RA [21]. Additionally, for patients with OA in the hip and/or the knee, exercise improves physical function and lowers pain [16, 17].

For both RA patients and patients at increased risk for RA, the heart rate is controlled increasingly by the sympathetic nervous system in contrast to the parasympathetic nervous system. This results in a lower heart rate variability suggesting a higher level of stress [22, 23]. The onset of RA has also been linked to stress [6, 7, 24], and both Mindfulness Based Stress Reduction (MBSR) as well as internet-based cognitive-behavioral therapy have shown favorable outcomes, especially with regard to general wellbeing [25, 26]. For OA, a small pilot study showed a significant reduction of pain and improvement of function in patients who followed an 8-week meditation program. In OA patients, higher baseline “mindfulness” scores were also associated with a better response to exercise than patients with lower baseline mindfulness, suggesting again the synergistic effects of combining more disciplines within one intervention [27].

A multidisciplinary program based on a WFPD, exercise, and stress management showed favorable results for patients with coronary artery disease [28]. Although the separate components of this multidisciplinary lifestyle intervention were found to be beneficial for RA and OA patients, no studies have yet been conducted to investigate the effect of an integrated program for RA or OA.

The presence of low-grade inflammation is a feature of many chronic diseases including RA and OA [29]. In RA, a chronic autoimmune arthritis condition, the presence of low-grade inflammation—possibly intermediated by microbiome dysbiosis—may cause the breakdown of immune tolerance [29, 30]. Support for the mucosal origin of RA comes from the observation that part of the circulating RA-associated autoantibodies rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPA) are of mucosal origin [30]. Additionally, compared to healthy individuals, an altered, or dysbiotic, microbiome is seen in RA and its preclinical stage, with, among others, an overrepresentation of Lactobacillus salivarius and Prevotella copri [31]. As the microbiome is affected among others by diet, exercise, and stress, these lifestyle factors may therefore contribute to the pathogenesis of RA at mucosal sites [30,31,32,33].

Low-grade inflammation is also associated with metabolic syndrome, a combination of risk factors such as high fat mass (waist circumference), high blood pressure, high low-density lipoprotein (LDL), low high-density lipoprotein (HDL), high triglycerides, and high fasting glucose, which are very common in patients with OA [29, 34]. Levels of inflammatory mediators are higher in people with visceral adiposity, which may mediate the relationship between OA and obesity [35]. This has resulted in the denomination of metabolic syndrome-associated osteoarthritis (MSOA) as a specific form of OA [36]. MSOA is a chronic condition with limited treatment options (analgesics, nonsteroidal anti-inflammatory drugs (NSAIDs), and intra-articular glucocorticoids), and although guidelines for the treatment of OA also recommend exercise treatment, weight loss, and mental health interventions, they also emphasize the need for more studies, especially regarding multidisciplinary interventions.

The systemic impact of low-grade inflammation, microbiome dysbiosis, and increased (mostly visceral) fat mass also explains the frequent occurrence of comorbidities, such as diabetes and cardiovascular disease in patients with OA and RA [34, 37].

Research objective

The objective of Plants for Joints is to study the effects of a multidisciplinary lifestyle program in patients with (risk for) RA and in patients with MSOA. The program consists of a WFPD, exercise, and stress management and aims to lower disease activity in patients with RA (randomized controlled trial [RCT] 1), to lower the risk of RA [38] in patients with ACPA-positive arthralgia (RCT 2), or to improve the scores for pain, stiffness and function in patients with MSOA (RCT 3), all in comparison to usual care. An observational extension study is added to investigate adherence.

Design and methods


We designed three 16-week observer-blind RCTs with a waiting-list control group for patients with RA (RCT1), for patients at risk for RA, defined by ACPA-positive arthralgia (RCT 2) and for patients with MSOA (RCT 3) [39]. All participants receive the program, either directly or after participation in the control group.

Medication for RA is kept stable during the RCT (16 weeks for the intervention group, 32 weeks for the control group) whenever possible. DMARD changes (in RA patients) and intercurrent corticosteroid administration is considered a protocol deviation and the reason for the change will be registered.

In a 2-year extension study, starting at the end of the 16-week lifestyle program, all patients receive continued online support and 6 additional, thematic and facultative meetings. During the extension study, we will investigate adherence to the lifestyle program in relation to long-term effects and success factors for and barriers to changing behavior.

Study visits are at baseline, 8 and 16 weeks during the RCT, at 8 and 16 weeks for the waiting-list control group after entering the intervention, and every 6 months during the extension period.

A schedule of the intervention and the measurements during the 16-week RCT is shown in Fig. 1. Figure 2 shows a comprehensive scheme based on the SPIRIT format and includes the intervention phase for the waiting-list control group and the 2-year extension study. The SPIRIT Checklist is available as an additional file (supplement 1) [39].

Fig. 1
figure 1

Schedule of intervention and measurements during the randomized controlled trial (RCT). DAS28, disease activity score based on 28 joints; RA, rheumatoid arthritis; HRV, heart rate variability; DEXA, dual-energy x-ray absorptiometry; MRI, magnetic resonance imaging

Fig. 2
figure 2

SPIRIT figure with phases of the study and data collection time points. (X) = measurement only for waiting-list control group. RCT, randomized controlled trial; yr, year; ext, extension; DAS28, disease activity score based on 28 joints; WOMAC, Western Ontario and McMaster Universities Osteoarthritis Index; RA, rheumatoid arthritis; PROMIS®, Patient Reported Outcomes Measurement Information System; DEXA, dual-energy x-ray absorptiometry; LDL, low-density lipoprotein; HDL, high-density lipoprotein; ESR, erythrocyte sedimentation rate; HbA1c, hemoglobin A1c; MRI, magnetic resonance imaging; HRV, heart rate variability; EQ-5D-5L, EuroQol 5 dimensions 5 levels

Recruitment, selection, and randomization of participants

Subjects aged ≥ 18 years are recruited through rheumatologists, rehabilitation specialists, nurses and allied health care professionals at Reade and Amsterdam UMC (The Netherlands), and other regional hospitals or health centers. The main inclusion criteria are as follows: (RCT 1) RA according to the American College of Rheumatology (ACR)/European Alliance of Associations for Rheumatology (EULAR) 2010 criteria [40] with low to moderate disease activity (2.6 ≤ DAS28 ≤ 5.1) [41] and unchanged use of disease-modifying anti-rheumatic drugs (DMARDs) for 3 months or non-use of DMARDs; (RCT 2) arthralgia and positivity for ACPA [38]; and (RCT 3) OA in hip and/or knee, diagnosed according to the clinical criteria of the ACR (without age-criterion) [42, 43] and metabolic syndrome according to the criteria defined by the National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATP III) [44]. The main exclusion criteria are as follows: insufficient e-health competencies to fill in digital questionnaires and keep an online food diary, already following a predominantly plant-based diet, underweight (BMI < 18.5 kg/m2), pregnancy, and unwillingness to stop smoking for at least the duration of the RCT, if applicable.

The study has a parallel trial design in which patients are randomized in a 1:1 ratio by the researchers using CASTOR (an electronic database platform for data collection, management, and storage, with strictly defined user roles and patient management procedures, which keeps an audit trail) with a variable block randomization in block sizes of 2 and 4 (not stratified).

Both patients as well as study staff are not blinded for allocation. During measurements, a research nurse or other researcher, not involved in the study and not aware of allocation or phase of the study, will execute the examination for DAS28 (physical examination of the joints). Other primary and secondary outcomes are blinded by default (automized questionnaires or laboratory markers).


Subjects of all three RCTs participate in the same lifestyle program in mixed groups.

The program starts with a personal intake by a dietitian, reviewing general health, dietary habits, and physical activity. With a physical therapist, personal goals for physical activity are set (and reset at the beginning of the extension period). The lifestyle program consists of 10 group meetings (with 6–12 participants) for 2–3 h each (see supplement 2). During the program theoretical education about a WFPD, exercise, and stress is combined with a practical cooking class (with partner or relevant other person, in the first meeting), relaxation exercises and physical training, supported by podcasts, videos, and at-home exercises. The control group receives usual care, is advised not to change usual behavior, and enters the program after 16 weeks.

The WFPD is based on protocols by Ornish and Barnard [28, 45], although recommendations on fat are adapted to Dutch guidelines (20–35/40% of energy instead of low fat [max 10% of energy]). The proposed diet is in line with the 2015 Guidelines on Healthy Nutrition of the Health Council of the Netherlands. Subjects will be facilitated by means of fully elaborated week plans (developed by registered dietitians, in line with recommended daily allowances, see example in Fig. 3), and they will receive supplementation for vitamin B12 and D [46]. To promote weight loss, overweight and obese patients are motivated to limit meal frequency to three meals per day. The program contains a short “green fasting” protocol (see supplement 3) [9,10,11,12,13], as recommended by the program Ambassadors. The program Ambassadors are fifteen target group patients, who are involved in the development of the lifestyle program and the analyses. These lay experts had experienced improvement in their own health status with diet adaptations, exercise, and/or use of stress management techniques.

Fig. 3
figure 3

Example of a week menu

Recommendations for physical activity and exercise are based on the Dutch physical activity guidelines 2017 and the protocol by Ornish [28, 47]. Group exercise is focused on moderate exercise, fun, and group cohesion. Patients will be motivated to integrate physical activity in daily activities (example: walk/cycle more rather than sitting in a car or public transport) and search for possibilities to exercise in their neighborhood.

Stress management is based on protocols by De Brouwer et al. [48]. Subjects will receive psychoeducation on the effects of stress on health and on stress management, as well as guided practice and home exercises (supported by tools, such as audio/Apps) on relaxation techniques and breathing and visualization exercises, as well as coaching on sleep [48].

A specification of the subjects covered in the 10 group meetings is available in supplement 2.

During the 2-year extension study, 6 facultative meetings will be organized for participants on varying subjects from the three categories (examples: weight loss, how to stay active, self-compassion). After the 16-week intervention, medication of subjects with RA with minimal disease activity (DAS < 2.6) will be tapered by the participants’ rheumatologists, who are supplied with a standardized scheme (see supplement 4). If disease activity increases after tapering, medication will again be increased back to the previous step. For participants in the MSOA group, pain medication will be monitored.


Primary outcome measures

Main endpoints are the differences between mean changes in the intervention versus control groups from 0 to 16 weeks in:

  • RCT 1: the DAS28 based on erythrocyte sedimentation rate (ESR), number of swollen joints and tender joints and general health based on the score on a visual analog scale [49] (measured by a blinded research nurse) for RA patients.

  • RCT 2: the RA-risk score (combined score based on RA prevalence in first degree relatives, alcohol consumption, duration, intermittency and location of symptoms, pain, morning stiffness, self-perceived swelling of joints and antibody status) [38] in ACPA-positive arthralgia patients. If a subject develops RA during the study, the RA-risk score will be set to 13 points, the highest possible score.

  • RCT 3: scores on pain, stiffness, and function, combined in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) index [50] for OA patients, measured by the WOMAC questionnaire [51].

Main endpoint for the 2-year extension study for all three groups is the change in adherence from 0 to 24 months, based on an adapted version of the Lifestyle index adherence score as developed by Ornish et al [52]:

$$ \left(\mathrm{t}+\left(\left[\mathrm{u}/6+\mathrm{v}/60\right]/2\right)+\left(\left[\mathrm{x}/5+\mathrm{y}/150\right]/2\right)+\mathrm{z}\right)/4 $$

In which t = attendance meetings, u = stress reduction activities days per week, v = stress reduction activities minutes per week, x = exercise days per week, y = exercise minutes per week, and z = adherence to diet.

Adherence to diet (z) is defined as ((grams of fiber per 1000 kilocalories/14) + (10/en% SFA))/2 whereby “en% SFA” is defined as the percentage of total kilocalories a day from saturated fatty acids (SFAs). In the original model by Ornish, z was defined by total fat and cholesterol intake. Since our protocol is not based on a low-fat WFPD, we changed these vectors into fiber and saturated fatty acids (SFAs) as indicators for a WFPD.

Secondary outcome measures

Secondary outcomes are the same for all groups in the three RCTs: RA, ACPA-positive arthralgia, and MSOA, unless otherwise specified. Quality of life-related outcomes measured are self-reported physical, mental and, social health, using the validated Dutch-Flemish Patient Reported Outcomes Measurement Information System (PROMIS®) [53]. In order to select the most important secondary patient reported outcomes, we consulted the Ambassadors. From a list of 13 physical, mental and social item banks (see supplement 5), they chose physical function, fatigue, and pain interference as most important. We added depression to this list, since it is strongly associated with the onset of RA [7, 24]. Other secondary outcomes are waist circumference, fat mass (measured by dual-energy X-ray absorptiometry [DEXA]), blood pressure, LDL, HDL, triglycerides, fasting glucose, and ESR.

Other outcome measures

Other outcomes related to body composition and metabolism are body weight, height and muscle mass (measured by DEXA). Fifty MSOA patients (30 from the intervention group and 20 from the control group) will be recruited for MRI examination of visceral adipose tissue (VAT), liver fat, and intramuscular fat in the thigh muscle. For the liver and the thigh muscle, the fat content will be determined. In VAT and the thigh muscle, we will characterize the fatty acid distribution based on the peaks in the spectrum representing double and single bonds in the carbon backbone.

Performance-based physical functioning will be measured by grip strength [54] and per get-up-and-go test [55].

Diet (4-7 consequent days digital diary) will be measured using the Dutch ‘Eetmeter’ by ‘Voedingscentrum’ (The Netherlands Nutrition Centre), a validated food diary based on the Dutch food composition database. It is applicable through internet and in the form of an App [56]. Stress is measured using the perceived stress scale (PSS) [57]. In addition, biophysical markers for stress are measured using morning salivary cortisol and heart rate variability (as measured on electrocardiography). Physical activity level will be based on activity data captured by Fitbit Inspire HR wristbands.

We will track metabolic markers such as blood pressure, lipid profile, fasting glucose, and HbA1c and measure pathogenic biomarkers such as RF and ACPA, C-reactive protein, fecal, and oral saliva microbiota 16S composition as well as plasma metabolome changes. Other biomarkers related to dietary intake such as blood markers for folic acid, vitamin B12, calcidiol, hemoglobin, ferritin, leukocytes, thrombocytes, mean corpuscular hemoglobin, creatinine, alanine transaminase, and aspartate transaminase will be measured.

An economic evaluation will be performed to assess the cost-effectiveness of the multidisciplinary lifestyle program compared with usual care for quality-adjusted life-years (QALYs) and the primary outcome measures in all three patient groups. The EQ-5D-5L will be used to measure health-related quality of life. The patients’ EQ-5D-5 L health states will be converted into utility values using the Dutch tariff [58]. QALYs will be estimated by multiplying the patients’ time spent in a certain health state by the respective utility value. Costs will be assessed from a societal (among others informal care, absenteeism costs) and a healthcare perspective [59].

A detailed overview of the measurements is available in supplement 5.

Sample size calculation

Based on α = 0.05 and power (1-β) = 0.80, effects ranged from 0.4 to 1.0 decreases for the DAS28 (estimated from component data of the DAS28 in the case of the trial by Kjeldsen Kragh et al.) with standard deviations (SD) ranging from 0.6–1.0 [12, 14]. The minimal clinically important improvement (MCII) in the DAS28, however, increases with higher baseline values and vice versa [60]. In the range of our inclusion criterion of DAS28 (between 2.6 and 5.1), the MCII is 0.8. Sköldstam et al. reported a difference in the DAS28 of 0.5 in 12 weeks [14]. In our 16-week study, we expect an additional effect on top of that provided by diet alone, due to the combination with exercise and stress management. Based on clinically relevant effect sizes of delta 0.8 with a SD of 1.2 for the DAS28, α of 0.05, and β of 0.2, we need a sample size of 56.

For OA patients, we found effects ranging from 2.2 to 2.8 for WOMAC pain (OA) and 5.7 to 10 for WOMAC function (OA) and standard deviations (SD) ranging from 0.4 to 0.6 with an exceptional 3.1 for WOMAC pain and 1.4 to 3.1 with an exceptional 10.9 for WOMAC function [15, 61, 62]. Based on these studies, we estimated that a power of 0.80 is feasible with a total of 60–70 subjects (intervention + control group) and planned to aim for 80 subjects for both RA as well as OA patients (total 160 patients) based on a possible dropout rate of approximately 20%.

For patients with ACPA-positive arthralgia, we added a pilot group of 16 participants (n = 8 intervention group, n = 8 waiting-list control group).

Statistical analysis

At baseline, half-way (8 weeks) and at the end of the study (16 weeks) outcomes are measured (see supplement 5 for a specification of the measurements).

After conclusion of the randomized controlled trial, data will be cleaned, verified by two researchers, and inspected for errors, inconsistencies, and incomplete information. Outliers will be inspected and corrected if necessary.

Primary outcomes DAS28, RA risk-scores, and WOMAC (all continuous variables) at 8 and 16 weeks in the intervention group will be compared with outcomes at 8 and 16 weeks in the control group, adjusted for baseline scores. Intention-to-treat analyses will be performed, with additional per-protocol analyses. For the analyses, a repeated measures mixed model will be used with random effect for the subjects and fixed effects for group (intervention or control) and baseline values for DAS28, RA risk-score, or WOMAC.

Secondary outcome measures (physical function, fatigue, pain interference, depression, waist circumference, fat mass, blood pressure, LDL, HDL, triglycerides, fasting glucose and ESR) will be analyzed the same way as the primary outcomes. Statistical tests will be limited to primary and secondary outcomes. For other outcomes, descriptive statistics will be used. We will analyze microbiome, remaining metabolic and stress-related outcomes separately and report results in dedicated articles.

In the extension study, the primary and secondary outcomes of the intervention study will become secondary outcomes, and adherence will be the primary outcome. These outcomes are analyzed in the same way as the intervention study, using the baseline, halfway, and end measurements from the 16-week intervention program, as well as 6-, 12-, and 18-month and end (24 month) measurements of the extension study. Intention-to-treat analyses will be performed, with additional per-protocol analyses. Since the extension study is observational, a within-subject analysis will be performed using a repeated measures mixed model with random effect for the subjects and fixed effects for baseline values.

P values < 0.05 will be considered to be significant.


The present paradigm of RA treatment is early recognition and prompt suppression of inflammation with drug therapy targeted to achieve and maintain remission or low disease activity [40]. Despite the success of intensified drug therapies, there are still unmet needs. Thirty percent of RA patients do not respond to the preferred medication, suffer from side effects, or become resistant to medication [63]. Also, 69% of RA patients are still limited by pain, fatigue, and reduced mobility [64], and the mortality gap between RA patients and the general population remains despite early aggressive treatment [65]. The unmet needs of RA patients, in combination with the underuse of the present knowledge of environmental risk factors for RA in clinical practice, call for an increased effort to investigate potentially effective non-pharmacologic options in the treatment of these diseases.

On the other hand, while treatment of OA comprises exercise treatment, weight loss, and mental health interventions, these lifestyle-related recommendations lack specificity and consensus [66].

The present protocol is in line with the gaps identified by the EULAR committees. For both RA and OA, more evidence on non-pharmacological interventions is needed with an emphasis on multidisciplinary approaches, including physical therapy and exercise, psychological support, and diet [66, 67].

A good example of a lifestyle program in which all these non-pharmacological disciplines are combined is the Ornish Program (USA, covered by most health insurance companies), based on a WFPD, exercise, and stress management. It has been shown to be effective for the treatment of coronary heart disease [28]. Since atherosclerosis and synovitis share pathological features [36, 68] and both RA as well as OA patients are at increased risk for cardiovascular disease, it is worthwhile to not only study the effect of this program on arthritis, but also on the factors that determine the risk of coronary heart disease.


The Plants for Joints diet is developed by registered dietitians and based on the Dutch dietary guidelines. The menus meet recommended daily allowances, except for vitamin B12 and D, which are supplemented. Menus are affordable and composed of readily available unprocessed plant-based foods. During the 16-week program, participants learn how to implement this diet into their own lifestyle, allowing for feasible, long-term adherence. The same strength is seen in exercise, stress management, and sleep: implementation of the recommendations is simple and easy to grasp.

We are the first to study a multidisciplinary lifestyle intervention based on more than two disciplines for (increased risk of) RA or MSOA in a randomized, single-blind, controlled trial. The addition of microbiome analyses provides us with the opportunity to study changes in the microbiome as a result of the intervention in relation to changes in disease activity.

We are also the first to study a plant-based diet in RA since the studies by Kjeldsen-Kragh in 1991 and Hafström in 2001 [12, 69], where they concluded that a plant-based diet had several favorable outcomes. Their population, however, was different than current RA patients, who are much more intensively treated and will have lower average baseline disease activity. By keeping medication stable during the trial and tapering it using a standardized scheme, we will be able to provide a realistic picture of the tapering potential.

For OA, we are the first to study a multidisciplinary lifestyle program based on a WFPD. An additional strength is that we have chosen for the particular group of MSOA patients which can be characterized by the systemic profile of unfavorable lifestyle, excessive visceral fat, possible microbiome dysbiosis, low-grade inflammation, and metabolic syndrome. Using MRI, we will study the effects of our intervention on visceral adipose tissue, hepatocellular fat, and intramyocellular fat in the MSOA population in relation to pain, function, and stifness (primary outcome). In this study both the effect of the lifestyle intervention as well as the possible pathophysiological pathways are addressed, thus providing a holistic overview of contributing mechanisms.


A double-blind RCT is not possible in this setting. Also, the many measurements may be a burden for the participants and may interfere with adherence. Furthermore, participation is limited to patients with good literacy and e-health competencies for efficiency reasons. Participation obviously was also limited to patients willing to change their lifestyle. In generalizing findings of our study, this relatively high level of motivation has to be taken into account. In addition, the design leaves out the patient group with low disease activity (DAS28 < 2.6) which is estimated at 40–60% of RA patients [70, 71].


The results of studies on the effectiveness of an (almost) WFPD for RA and OA patients are promising but have not yet been combined with other lifestyle interventions, despite the potential synergistic effects. Therefore, we wish to study the combined effect (including cost-effectiveness) of a WFPD, exercise, and stress management on disease activity in RA patients, RA risk-score in ACPA-positive arthralgia patients, and pain, function, and stiffness in MSOA patients. Long-term adherence will be studied in a 2-year extension study. We will provide evidence on the level of effectiveness of a multidisciplinary lifestyle intervention, which will help to further specify the role of these non-pharmacological treatments in patients with (an increased risk of) RA and MSOA.

Trial status

Patient recruitment began in May 2019. The trial is currently underway. Article based on protocol version 7.0 (March 2021). Recruitment of patients is expected to be completed in August 2021.

Availability of data and materials

In addition to the material in the supplements of this article, information on this trial can be obtained upon request.

No professional writers were used for this article, and they will be not used for the publication of the results.

Trial results will be communicated to participants through e-mail newsletters and webinars or seminars. There are no restrictions posed on publication. The project includes the development of an implementation plan for dissemination among health professionals and possible implementation of the program when it shows to be effective.



Anti-citrullinated protein antibody


American College of Rheumatology


Disease activity score in 28 joints


Dual-energy X-ray absorptiometry


Disease-modifying anti-rheumatic drug


Percentage of energy (kilocalories)


Erythrocyte sedimentation rate


European Alliance of Associations for Rheumatology


High-density lipoprotein


Heart rate variability


Low-density lipoprotein


Minimal clinically important improvement


Magnetic resonance imaging


Metabolic syndrome-associated osteoarthritis


Nonsteroidal anti-inflammatory drug




Patient-Reported Outcomes Measurement Information System


Perceived stress scale


Quality-adjusted life-year


Rheumatoid arthritis


Randomized controlled trial


Saturated fatty acid


Standard Protocol Items: Recommendations for Interventional Trials


Visceral adipose tissue


Whole food plant-based diet


Western Ontario and McMaster Universities Osteoarthritis Index


National Cholesterol Education Program Adult Treatment Panel III


  1. Hu Y, Sparks JA, Malspeis S, Costenbader KH, Hu FB, Karlson EW, et al. Long-term dietary quality and risk of developing rheumatoid arthritis in women. Ann Rheum Dis. 2017;76(8):1357–64.

    CAS  Article  PubMed  Google Scholar 

  2. de Hair MJ, Landewe RB, van de Sande MG, van Schaardenburg D, van Baarsen LG, Gerlag DM, et al. Smoking and overweight determine the likelihood of developing rheumatoid arthritis. Ann Rheum Dis. 2013;72(10):1654–8.

    Article  PubMed  Google Scholar 

  3. Crowson CS, Matteson EL, Davis JM 3rd, Gabriel SE. Contribution of obesity to the rise in incidence of rheumatoid arthritis. Arthritis Care Res (Hoboken). 2013;65(1):71–7.

    Article  Google Scholar 

  4. Turk SA, van Beers-Tas MH, van Schaardenburg D. Prediction of future rheumatoid arthritis. Rheum Dis Clin North Am. 2014;40(4):753–70.

    Article  PubMed  Google Scholar 

  5. WHO. WHO: Priority Medicines for Europe and the World 2013 Update. Accessed on: March 22 2018.

  6. van Middendorp H, Evers AW. The role of psychological factors in inflammatory rheumatic diseases: From burden to tailored treatment. Best Pract Res Clin Rheumatol. 2016;30(5):932–45.

    Article  PubMed  Google Scholar 

  7. Lee YC, Agnew-Blais J, Malspeis S, Keyes K, Costenbader K, Kubzansky LD, et al. Post-Traumatic Stress Disorder and Risk for Incident Rheumatoid Arthritis. Arthritis Care Res (Hoboken). 2016;68(3):292–8.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Glyn-Jones S, Palmer AJ, Agricola R, Price AJ, Vincent TL, Weinans H, et al. Osteoarthritis. Osteoarthritis. Lancet. 2015;386(9991):376–87.

    CAS  Article  PubMed  Google Scholar 

  9. Skoldstam L, Larsson L, Lindstrom FD. Effect of fasting and lactovegetarian diet on rheumatoid arthritis. Scand J Rheumatol. 1979;8(4):249–55.

    CAS  Article  PubMed  Google Scholar 

  10. Uden AM, Trang L, Venizelos N, Palmblad J. Neutrophil functions and clinical performance after total fasting in patients with rheumatoid arthritis. Ann Rheum Dis. 1983;42(1):45–51.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  11. Hafstrom I, Ringertz B, Gyllenhammar H, Palmblad J, Harms-Ringdahl M. Effects of fasting on disease activity, neutrophil function, fatty acid composition, and leukotriene biosynthesis in patients with rheumatoid arthritis. Arthritis Rheum. 1988;31(5):585–92.

    CAS  Article  PubMed  Google Scholar 

  12. Kjeldsen-Kragh J, Haugen M, Borchgrevink CF, Laerum E, Eek M, Mowinkel P, et al. Controlled trial of fasting and one-year vegetarian diet in rheumatoid arthritis. Lancet. 1991;338(8772):899–902.

    CAS  Article  PubMed  Google Scholar 

  13. Abendroth A, Michalsen A, Ludtke R, Ruffer A, Musial F, Dobos GJ, et al. Changes of Intestinal Microflora in Patients with Rheumatoid Arthritis during Fasting or a Mediterranean Diet. Forsch Komplementmed. 2010;17(6):307–13.

    Article  PubMed  Google Scholar 

  14. Skoldstam L, Hagfors L, Johansson G. An experimental study of a Mediterranean diet intervention for patients with rheumatoid arthritis. Ann Rheum Dis. 2003;62(3):208–14.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  15. Messier SP, Mihalko SL, Legault C, Miller GD, Nicklas BJ, DeVita P, et al. Effects of intensive diet and exercise on knee joint loads, inflammation, and clinical outcomes among overweight and obese adults with knee osteoarthritis: the IDEA randomized clinical trial. JAMA. 2013;310(12):1263–73.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  16. Fransen M, McConnell S, Harmer AR, Van der Esch M, Simic M, Bennell KL. Exercise for osteoarthritis of the knee: a Cochrane systematic review. Br J Sports Med. 2015;49(24):1554–7.

    Article  PubMed  Google Scholar 

  17. Fransen M, McConnell S, Hernandez-Molina G, Reichenbach S. Exercise for osteoarthritis of the hip. Cochrane Database Syst Rev. 2014;4:CD007912.

    Google Scholar 

  18. Clinton CM, O'Brien S, Law J, Renier CM, Wendt MR. Whole-foods, plant-based diet alleviates the symptoms of osteoarthritis. Arthritis. 2015;2015:708152–9.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Di Giuseppe D, Bottai M, Askling J, Wolk A. Physical activity and risk of rheumatoid arthritis in women: a population-based prospective study. Arthritis Res Ther. 2015;17(1):40.

    Article  PubMed  PubMed Central  Google Scholar 

  20. de Jong Z, Munneke M, Zwinderman AH, Kroon HM, Jansen A, Ronday KH, et al. Is a long-term high-intensity exercise program effective and safe in patients with rheumatoid arthritis? Results of a randomized controlled trial. Arthritis Rheum. 2003;48(9):2415–24.

    Article  PubMed  Google Scholar 

  21. Hurkmans E, van der Giesen FJ, Vliet Vlieland TP, Schoones J, Van den Ende EC. Dynamic exercise programs (aerobic capacity and/or muscle strength training) in patients with rheumatoid arthritis. Cochrane Database Syst Rev. 2009;4:CD006853.

    Google Scholar 

  22. Evrengul H, Dursunoglu D, Cobankara V, Polat B, Seleci D, Kabukcu S, et al. Heart rate variability in patients with rheumatoid arthritis. Rheumatol Int. 2004;24(4):198–202.

    Article  PubMed  Google Scholar 

  23. Koopman FA, Tang MW, Vermeij J, de Hair MJ, Choi IY, Vervoordeldonk MJ, et al. Autonomic Dysfunction Precedes Development of Rheumatoid Arthritis: A Prospective Cohort Study. EBioMedicine. 2016;6:231–7.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  24. O'Donovan A, Cohen BE, Seal KH, Bertenthal D, Margaretten M, Nishimi K, et al. Elevated risk for autoimmune disorders in iraq and afghanistan veterans with posttraumatic stress disorder. Biol Psychiatry. 2015;77(4):365–74.

    Article  PubMed  Google Scholar 

  25. Pradhan EK, Baumgarten M, Langenberg P, Handwerger B, Gilpin AK, Magyari T, et al. Effect of Mindfulness-Based Stress Reduction in rheumatoid arthritis patients. Arthritis Rheum. 2007;57(7):1134–42.

    Article  PubMed  Google Scholar 

  26. Ferwerda M, van Beugen S, van Middendorp H, Spillekom-van Koulil S, Donders ART, Visser H, et al. A tailored-guided internet-based cognitive-behavioral intervention for patients with rheumatoid arthritis as an adjunct to standard rheumatological care: results of a randomized controlled trial. Pain. 2017;158(5):868–78.

    Article  PubMed  Google Scholar 

  27. Lee AC, Harvey WF, Price LL, Han X, Driban JB, Wong JB, et al. Mindfulness Is Associated With Treatment Response From Nonpharmacologic Exercise Interventions in Knee Osteoarthritis. Arch Phys Med Rehabil. 2017;98(11):2265–73 e1.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Ornish D, Scherwitz LW, Billings JH, Brown SE, Gould KL, Merritt TA, et al. Intensive lifestyle changes for reversal of coronary heart disease. JAMA. 1998;280(23):2001–7.

    CAS  Article  PubMed  Google Scholar 

  29. Furman D, Campisi J, Verdin E, Carrera-Bastos P, Targ S, Franceschi C, et al. Chronic inflammation in the etiology of disease across the life span. Nat Med. 2019;25(12):1822–32.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  30. Zaiss MM, Joyce Wu HJ, Mauro D, Schett G, Ciccia F. The gut-joint axis in rheumatoid arthritis. Nat Rev Rheumatol. 2021;17(4):224–37.

    Article  PubMed  Google Scholar 

  31. Jethwa H, Abraham S. The evidence for microbiome manipulation in inflammatory arthritis. Rheumatology (Oxford). 2017;56(9):1452–60.

    CAS  PubMed  Google Scholar 

  32. van Delft MAM, van der Woude D, Toes REM, Trouw LA. Secretory form of RA-associated autoantibodies in serum are mainly of the IgM isotype. Ann Rheum Dis. 2019;78(1):146–8.

    CAS  Article  PubMed  Google Scholar 

  33. Clemente JC, Manasson J, Scher JU. The role of the gut microbiome in systemic inflammatory disease. BMJ. 2018;360:j5145.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Puenpatom RA, Victor TW. Increased prevalence of metabolic syndrome in individuals with osteoarthritis: an analysis of NHANES III data. Postgrad Med. 2009;121(6):9–20.

    Article  PubMed  Google Scholar 

  35. Sekar S, Shafie SR, Prasadam I, Crawford R, Panchal SK, Brown L, et al. Saturated fatty acids induce development of both MetS and OA in rats. Sci Rep. 2017;7(1):46457.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  36. Courties A, Sellam J, Berenbaum F. Metabolic syndrome-associated osteoarthritis. Curr Opin Rheumatol. 2017;29(2):214–22.

    CAS  Article  PubMed  Google Scholar 

  37. Hansildaar R, Vedder D, Baniaamam M, Tausche AK, Gerritsen M, Nurmohamed MT. Cardiovascular risk in inflammatory arthritis: rheumatoid arthritis and gout. Lancet Rheumatol. 2021;3(1):e58–70.

    Article  PubMed  Google Scholar 

  38. van de Stadt LA, Witte BI, Bos WH, van Schaardenburg D. A prediction rule for the development of arthritis in seropositive arthralgia patients. Ann Rheum Dis. 2013;72(12):1920–6.

    Article  PubMed  Google Scholar 

  39. Chan AW, Tetzlaff JM, Altman DG, Laupacis A, Gotzsche PC, Krleza-Jeric K, et al. SPIRIT 2013 statement: defining standard protocol items for clinical trials. Ann Intern Med. 2013;158(3):200–7.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Aletaha D, Neogi T, Silman AJ, Funovits J, Felson DT, Bingham CO 3rd, et al. 2010 rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Ann Rheum Dis. 2010;69(9):1580–8.

    Article  PubMed  Google Scholar 

  41. Fransen J, van Riel PL. DAS remission cut points. Clin Exp Rheumatol. 2006;24(6 Suppl 43):S-29–32.

    Google Scholar 

  42. Altman R, Alarcon G, Appelrouth D, Bloch D, Borenstein D, Brandt K, et al. The American College of Rheumatology criteria for the classification and reporting of osteoarthritis of the hip. Arthritis Rheum. 1991;34(5):505–14.

    CAS  Article  PubMed  Google Scholar 

  43. Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, et al. Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum. 1986;29(8):1039–49.

    CAS  Article  PubMed  Google Scholar 

  44. 3rd Report of the NCEP Expert Panel on High Blood Cholesterol in Adults. Circulation. 2002;106(25):3143–421.

  45. Barnard N, Gloede L, Cohen J, Jenkins DJ, Turner-McGrievy G, Green AA, et al. A low-fat vegan diet elicits greater macronutr changes. J Am Diet Assoc. 2009;109(2):263–72.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Melina V, Craig W, Levin S. Position of the Academy: Vegetarian Diets. J Acad Nutr Diet. 2016;116(12):1970–80.

    Article  PubMed  Google Scholar 

  47. Gezondheidsraad. Beweegrichtlijnen 2017. Accessed on: March 29 2018. Link:

  48. de Brouwer SJ, Kraaimaat FW, Sweep FC, Donders RT, Eijsbouts A, van Koulil S, et al. Psychophysiological responses to stress in patients with RA. PLoS One. 2011;6(12):e27432.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  49. van Riel PL. Provisional guidelines for measuring disease activity in clinical trials on rheumatoid arthritis. Br J Rheumatol. 1992;31(12):793–4.

    Article  PubMed  Google Scholar 

  50. Bellamy N, Buchanan WW, Goldsmith CH, Campbell J, Stitt LW. Validation study of WOMAC: a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee. J Rheumatol. 1988;15(12):1833–40.

    CAS  PubMed  Google Scholar 

  51. Roorda LD, Jones CA, Waltz M, Lankhorst GJ, Bouter LM, van der Eijken JW, et al. Satisfactory cross cultural equivalence of the Dutch WOMAC in patients with hip osteoarthritis waiting for arthroplasty. Ann Rheum Dis. 2004;63(1):36–42.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  52. Ornish D, Lin J, Chan JM, Epel E, Kemp C, Weidner G, et al. Effect of comprehensive lifestyle changes on telomerase activity and telomere length in men with biopsy-proven low-risk prostate cancer: 5-year follow-up of a descriptive pilot study. Lancet Oncol. 2013;14(11):1112–20.

    CAS  Article  PubMed  Google Scholar 

  53. Dutch-Flemish PROMIS. Link:

  54. Roberts HC, Denison HJ, Martin HJ, Patel HP, Syddall H, Cooper C, et al. A review of the measurement of grip strength in clinical and epidemiological studies: towards a standardised approach. Age Ageing. 2011;40(4):423–9.

    Article  PubMed  Google Scholar 

  55. Piva SR, Fitzgerald GK, Irrgang JJ, Bouzubar F, Starz TW. Get up and go test in patients with knee osteoarthritis. Arch Phys Med Rehabil. 2004;85(2):284–9.

    Article  PubMed  Google Scholar 

  56. Ocke M, Dinnissen C, Stafleu A, de Vries J, van Rossum C. Relative Validity of MijnEetmeter: A Food Diary App for Self-Monitoring of Dietary Intake. Nutrients. 2021;13(4).

  57. Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav. 1983;24(4):385–96.

    CAS  Article  PubMed  Google Scholar 

  58. Versteegh M. Impact on the Incremental Cost-Effectiveness Ratio of Using Alternatives to EQ-5D in a Markov Model for Multiple Sclerosis. Pharmacoeconomics. 2016;34(11):1133–44.

    Article  PubMed  PubMed Central  Google Scholar 

  59. Kanters TA, Bouwmans CAM, van der Linden N, Tan SS, Hakkaart-van RL. Update of the Dutch manual for costing studies in health care. PLoS One. 2017;12(11):e0187477.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  60. Aletaha D, Funovits J, Ward MM, Smolen JS, Kvien TK. Perception of improvement in patients with rheumatoid arthritis varies with disease activity levels at baseline. Arthritis Rheum. 2009;61(3):313–20.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  61. Messier SP, Loeser RF, Miller GD, Morgan TM, Rejeski WJ, Sevick MA, et al. Exercise and dietary weight loss in overweight and obese older adults with knee osteoarthritis: the Arthritis, Diet, and Activity Promotion Trial. Arthritis Rheum. 2004;50(5):1501–10.

    Article  PubMed  Google Scholar 

  62. Miller GD, Nicklas BJ, Davis C, Loeser RF, Lenchik L, Messier SP. Intensive weight loss program improves physical function in older obese adults with knee osteoarthritis. Obesity (Silver Spring). 2006;14(7):1219–30.

    Article  Google Scholar 

  63. Hazlewood G, Barnabe C, Tomlinson G, Marshall D, Devoe DJ, Bombardier C. MTX monother & MTX comb ther with trad & biol DMARDs for RA. CDSR. 2016:CD010227.

  64. Sloot R, Flinterman L, Heins M, Lafeber M, Boeije H, Poos R, et al. Reumatische aandoeningen in Nederland - Ervaringen en kengetallen. NIVEL: Utrecht; 2016.

    Google Scholar 

  65. Holmqvist M, Ljung L, Askling J. Mortality following new-onset RA. Ann Rheum Dis. 2018;77(1):85–91.

    Article  PubMed  Google Scholar 

  66. Fernandes L, Hagen KB, Bijlsma JW, Andreassen O, Christensen P, Conaghan PG, et al. EULAR recommendations for the non-pharmacological core management of hip and knee osteoarthritis. Ann Rheum Dis. 2013;72(7):1125–35.

    Article  PubMed  Google Scholar 

  67. Combe B, Landewe R, Daien CI, Hua C, Aletaha D, Alvaro-Gracia JM, et al. 2016 update of the EULAR recommendations for the management of early arthritis. Ann Rheum Dis. 2017;76(6):948–59.

    Article  PubMed  Google Scholar 

  68. Sattar N, McCarey DW, Capell H, McInnes IB. Explaining how "high-grade" systemic inflammation accelerates vascular risk in rheumatoid arthritis. Circulation. 2003;108(24):2957–63.

    Article  PubMed  Google Scholar 

  69. Hafstrom I, Ringertz B, Spangberg A, von Zweigbergk L, Brannemark S, Nylander I, et al. A vegan diet free of gluten improves the signs and symptoms of rheumatoid arthritis: the effects on arthritis correlate with a reduction in antibodies to food antigens. Rheumatology (Oxford). 2001;40(10):1175–9.

    CAS  Article  PubMed  Google Scholar 

  70. Versteeg GA, Steunebrink LMM, Vonkeman HE, Ten Klooster PM, van der Bijl AE, van de Laar M. Long-term disease and patient-reported outcomes of a continuous treat-to-target approach in patients with early rheumatoid arthritis in daily clinical practice. Clin Rheumatol. 2018;37(5):1189–97.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  71. Einarsson JT, Willim M, Ernestam S, Saxne T, Geborek P, Kapetanovic MC. Prevalence of sustained remission in rheumatoid arthritis: impact of criteria sets and disease duration, a Nationwide Study in Sweden. Rheumatology (Oxford). 2019;58(2):227–36.

    Article  PubMed  Google Scholar 

Download references


Ambassadors of Plants for Joints, employees of the Reade Biobank (Toni de Jong-de Boer and Corrie Verdoold), interns (especially Anna Kretova, Melissa Dijkshoorn, Michelle Bischops and Marieke van de Put), registered dietitian Pauline Kortbeek, exercise coaches Sietske de Weers, Tom van Iersel, and Jobjan Blonk and relaxation/sleep coaches Nelleke Doornebal and Marieke Rinkema, professor Aart Nederveen (MRI), and MR technician Sandra van den Berg.


The RCT is funded by Reade (Amsterdam, the Netherlands), Reade Foundation (Amsterdam, the Netherlands), Stichting Vermeer 14 (private foundation, Amsterdam, the Netherlands), and W.M. de Hoop Stichting (private foundation, Bussum, the Netherlands). The extension study and microbiome studies are funded by ZonMw no. 555003210. MN is supported by a ZonMw VICI grant 2020 no. 09150182010020 (see The funders had no role in the design or execution of the study.

Author information

Authors and Affiliations



Study conception and fundraising: WW and DvS. Study design and statistical analysis: WW, DvS, ML, PW, HM, HvD, MN, CSdJ, and LvB. Patient recruitment: WW, CW. WW drafted the manuscript. DvS supervised the overall project. All authors read and approved the final version of the manuscript.

Corresponding author

Correspondence to Wendy Walrabenstein.

Ethics declarations

Ethics approval and consent to participate

The study protocol was approved by the Medical Ethical Committee of the Amsterdam University Medical Center, location VUmc, on April 26 2019 with protocol identification number NL66649.048.18. The trial was prospectively registered in the Netherlands Trial Register ( with identification numbers NL7800, NL7801, and NL7802 for the RA, MSOA, and APCA-positive arthralgia trials respectively. The trial registry includes all items from the World Health Organization Trial Registration Set and keeps an audit trail. All participants give written informed consent (including consent for collection and use of participant data) to the involved researchers or research associate. Subjects are informed about data storing and handling and are guaranteed on the discrete handling of their data (including pseudonymisation of body materials).

The trial was classified as “low-risk” by the Medical Ethical Committee and does not involve ancillary and post-trial care or compensation for any harm from those who suffer from trial participation. Medical care as needed will be supplied to the subject who discontinues the study. For subjects who discontinue the study due to the occurrence of adverse events potentially related to the intervention, follow-up will take place until the adverse event has abated, or until a stable situation has been reached, with findings being recorded in CASTOR (the digital case report form). However, given the nature of the intervention, this is not expected.

Due to the low risk level of this study monitoring is not mandatory. To ensure quality of this study, monitoring of source data handling will be performed locally. The monitoring will follow and check the standard operating procedure (SOP) of the Amsterdam University Medical Centers.

Serious adverse events need to be reported till end of study within the Netherlands. The investigator will report all serious adverse events to the sponsor without undue delay after obtaining knowledge of the events. All other adverse events will be followed until they have abated, or until a stable situation has been reached. Depending on the event, follow-up may require additional tests or medical procedures as indicated and/or referral to the general physician or a medical specialist.

Patients can discontinue participation at any time. The general practitioner of the patient receives information on participation of the patient during start of the program. Patients will decide with their physician whether discontinuation is necessary. Subjects can leave the study at any time for any reason if they wish to do so without any consequences. The investigator can decide to withdraw a subject from the study for urgent medical reasons.

The investigator/sponsor will notify the accredited ethical medical committee of the (premature) end of the study or of a temporary halt (including the reason) within a period of 8 weeks. Within 1 year after the end of the study, the investigator/sponsor will submit a final study report with the results of the study, including any publications/abstracts of the study, to the accredited ethical medical committee.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplement 1.

SPIRIT checklist

Additional file 2: Supplement 2.

Plants for Joints Program

Additional file 3: Supplement 3.

Summary fasting protocol

Additional file 4: Supplement 4.

Tapering scheme medication

Additional file 5: Supplement 5.

Detailed overview of measurements

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Walrabenstein, W., van der Leeden, M., Weijs, P. et al. The effect of a multidisciplinary lifestyle program for patients with rheumatoid arthritis, an increased risk for rheumatoid arthritis or with metabolic syndrome-associated osteoarthritis: the “Plants for Joints” randomized controlled trial protocol. Trials 22, 715 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: