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Recruitment of patients with de novo Parkinson disease: successful strategies in a randomized exercise clinical trial
© The Author(s). 2018
- Received: 17 November 2017
- Accepted: 3 October 2018
- Published: 14 November 2018
Recruitment of sufficient patients with Parkinson disease into clinical trials is a barrier to successful, timely study completion. Non-pharmacologic studies have shown to be even more challenging for recruitment, despite some studies focusing on de novo Parkinson disease populations. This paper describes successful recruitment techniques from a randomized exercise clinical trial in Parkinson disease.
Several recruitment strategies were used to enroll de novo patients with Parkinson disease into a year-long clinical trial. Strategies focused on infrastructure included fast-track clinic scheduling, weekly research meetings, an established clinical repository, real-time clinic recruitment, and outreach to the community. The nature of the study facilitated recruitment by offering a wait-listed control group, exercise at a local fitness center with a paid membership, and collection of data by shipping equipment foregoing some visits. An experienced nurse study coordinator involved in recruitment and training of the principal investigator in recruitment of minorities enhanced overall recruitment. Finally, the patient population chosen for this study, patients with de novo Parkinson disease, may be more likely to enroll in an exercise study than patients with later stage disease.
Seventy-six patients with de novo Parkinson disease were successfully enrolled into the exercise clinical trial from a single site.
Targeted recruitment strategies were successful in this study. Additional modifications to the study protocol, such as eliminating treadmill stress tests before randomization, travel to an urban downtown location for study visits, and a relatively healthy Parkinson disease population, may also have impacted this study. These strategies could all be adopted for other studies in Parkinson disease, neurodegenerative diseases, or other chronic disorders.
Clinicaltrials.gov, NCT01506479. Registered on 10 January 2012.
- Parkinson disease
- Clinical trial
- Treadmill training
- De novo
Recruitment of adequate numbers of suitable patients for randomized clinical trials (RCTs) is frequently a major challenge in successful, timely completion of these studies . Only 31% of RCTs complete recruitment on time and only a minority of RCTs recruit to the original target, even with an extension . These problems are also seen in the recruitment of patients with Parkinson disease (PD) . Recruitment for non-pharmacological intervention studies may be even more challenging, especially when the intervention is readily available to the patient, such as in physical therapy studies .
There are four critical domains that have been previously reported to be influential to recruitment: infrastructure; nature of the research; recruiter characteristics; and patient characteristics . The strategies that will be described were performed at a tertiary movement disorder clinic that had nine movement disorder neurologists, two movement disorder fellows, two nurse study coordinators, two non-nurse study coordinators, two research assistants, a research administrator, videographer, database technician, and database manager. The movement disorder neurologists saw approximately 7000 patients per year, with 43% of them having PD.
Fast-track scheduling: All new patients to the clinic were scheduled through a centralized process within the Department of Neurology. After Institutional Review Board (IRB) approval of the exercise RCT, clinic schedulers were trained to ask prospective patients with PD if they had been treated with PD medication. If the patient had not, the patient was labeled “de novo” and one of the two study neurologists was contacted to see the patient. Patients with de novo PD were “fast-tracked”: seen within one week for a clinical evaluation, with many patients seen within 48 h. Patients confirmed to have de novo PD by the investigator, not requiring PD medication, and meeting inclusion criteria were recruited into the exercise RCT if they were interested in enrolling.
Research meetings: Meetings within the clinic occurred every Monday morning in order to review the current roster of recruiting studies, the numbers of enrolled individuals, and deadlines to reach recruitment milestones. All neurologists, fellows, study coordinators, and research assistants attended the meeting. PD studies were discussed by category of PD (such as de novo), inclusion and exclusion criteria were reviewed, number of individuals enrolled updated, and the number needed to fill the study were confirmed. Additional up-to-date reports from the study coordinator and/or research assistant and the study principal investigator (PI) were provided. Based on this process, the PD exercise RCT was discussed at the meeting at least twice monthly, with reminders to the faculty to refer any patients with de novo PD to the study team.
Clinical repository: Each new patient was consented for enrollment into an IRB-approved repository and videotaped ; the treating neurologist completed a database form with basic clinical information (Additional file 1). The data from the form were entered into a database, which could be quickly queried to ascertain specified patient populations for studies that were IRB-approved. Patients who enrolled in the repository were asked whether they agreed to be contacted for future studies. In addition to investigator data pulls, the database manager could also program the system to provide a research study alert sheet (“yellow form”) that was attached to each follow-up patient chart for those individuals in the repository who qualified for a particular study. This prompted the treating neurologist to recruit the patient for the identified study. Database pulls and study alert sheet were used to identify patients with de novo PD as they were seen in the clinic.
Real-time clinic recruitment: The physical space of the clinic consisted of staff and faculty offices that were contiguous with the clinic rooms so that the patient could be recruited at the time of their clinical visit. For this PD exercise RCT, the majority of the patients met with a study coordinator, research assistant, or PI at the time of their clinical appointment. A patient information form/consent form was given to the individual with follow-up via phone by the study coordinator within one week. In addition, flyer postings (IRB-approved) were used in the waiting room and in clinic exam rooms. This captured additional patients at the time of their visit.
Nature of the research
Demographics of the participants
62.6 ± 9.7
Sex (% women)
Ethnicity (% Hispanic)
Body mass index (kg/m2)
27.5 ± 4.5
Time since symptoms started (years)
2.3 ± 1.8
Time since diagnosis (years)
0.8 ± 0.9
Hoehn &Yahr Stage II (%)
Montreal Cognitive Assessment
27.7 ± 1.1
Unified Parkinson Disease Rating Scale Score
23.3 ± 8.2
16.5 ± 6.6
Activities of daily living
6.2 ± 3.6
Parkinson Disease Quality of Life Score
7.6 ± 5.7
Step count total (average daily)
5498 ± 2886
Geographic distance from study site (n)
Within 15 miles of Chicago
> 15 miles from Chicago
It is widely reported that patients are more likely to agree to participate in research if they are asked by a medical doctor and that successful recruitment is frequently a team effort . This PD exercise RCT had two movement disorder neurologists who shared responsibilities on the study, which allowed for fast-tracking clinic patients with de novo PD, coverage of in-person clinic recruitment, and greater flexibility in scheduling in-person assessments. In addition, the assigned nurse study coordinator had a 25-year history working with patients with PD and had a successful history of recruiting patients with de novo PD. She was frequently available after hours to talk to possible participants, would attend symposia and recruiting events, and was willing to contact participants using social media or texting. Midway through the PD exercise RCT, one of the study neurologists joined a NIH study designed to increase minority enrollment of patients with de novo PD into a second PD clinical trial. This study required extensive training in the recruitment of minority individuals; after completion, the study team was able to increase minority enrollment into the PD exercise RCT as well. Although it is argued whether it is possible to teach the “art of recruitment,” the experience of the current study team may have played a role.
The decision to take part in a study relies on three principal domains: (1) altruism; (2) personal health benefit; and (3) patient’s trust . Personal health benefit may have been the largest contributor to recruitment in this exercise study, given the wealth of data that supports exercise as a therapeutic intervention in both healthy individuals and in PD. In addition, many of the patients received their clinical care in the recruiting clinic and this established relationship may have increased the patient’s trust and their likelihood to enroll. The design of the study may have increased the likelihood of recruitment as this exercise study enrolled patients with de novo PD. This patient population, as opposed to later stage patients, is more likely to be able to complete a long duration, labor-intensive exercise intervention. However, the patient characteristics were consistent across sites so this is not likely to have been a major contributor to the success at a single site. Patients with de novo PD need to be captured early in the disease course and may present to community neurologists initially. Two senior faculty members phoned general neurologists in the community who had previously referred patients to the program and described the PD exercise RCT and inclusion criteria. These calls yielded several de novo participants from two practices. Each community physician also received a letter from the study team when the individual enrolled, thanking them for the referral and detailing the specifics of the study. As part of the community outreach, faculty members hosted a yearly movement disorder symposium referring neurologists and patients, that typically drew 150–200 patients with PD, some of which are treated in the community. Research studies were highlighted as part of this program. Further outreach was done through several PD-related events, including Michael J. Fox Foundation events, during which recruitment occurs. In addition, a quarterly “PD101” symposium was started, specifically geared towards patients with early stage PD. A database pull identified patients who were within three years of disease onset and those patients were sent a personal invitation. Patients were also referred to PD101 by their treating neurologist. Data regarding the PD exercise RCT were included in the 3-h free seminar and the PI was available at the seminar to recruit.
Recruitment strategies and reason for success
Reason for success
Shortened time for entry into the clinic and subsequently to recruitment
Research meeting recruitment reviews
Reminder to clinicians of the study entry criteria every Monday morning before the week’s clinics, increasing real-time recruitment
Clinical repository enrollment
Allowed creation of reminder sheets for recruitment into the exercise study at the time of the patient’s clinic visit
Contiguous clinic and research space
Study coordinators could meet with the potential subject immediately at the time of the clinic visit
Wait-listed control group
All patients knew that they would be receiving an exercise intervention
Local exercise and paid gym memberships
Patients could exercise locally and reduce the need to drive into a high traffic urban center
Heart rate monitors could be mailed back to study team
Alleviated the need for patients to travel back to the research clinic to return equipment
Multiple neurologists on the study
Allowed for in-person recruitment and more options for research visit scheduling at all times by a study neurologist
Experienced RN study coordinator
Facilitated recruitment by multiple techniques: support groups, social media, and after hours
Focused minority recruitment training
Raised investigator awareness and resulted in increased numbers of minorities recruited
De novo PD population
May be more motivated to participate in an intensive one-year exercise study due to a milder phenotype
Outreach to local neurologists
Increased the numbers of patients referred from the community for recruitment
Parkinson disease 101 course started
Focus on de novo Parkinson disease allowed for targeted recruitment at the quarterly seminars
Suboptimal recruitment for RCTs can be a substantial barrier in the study and approval of new therapies for PD. This paper summarizes strategies that were used at an academic site to recruit 76 patients with de novo PD for an exercise RCT over a three-year period. This recruitment is high for exercise studies in PD. There have been only a few other studies that have successfully recruited this number of patients. Our group recruited 121 patients with PD who were on PD medications in a prior study for a 16 month study investigating flexibility training or aerobic training compared to home exercises, using many of the same recruitment methods described in this paper . Eighty patients were recruited for a study investigating treadmill exercise at high and low intensity compared to stretching for a three-month study and is most similar to our study, albeit shorter in length . Ninety-three patients were recruited for a treadmill study compared to controls for six months, but only 34 participants were available at the end of the study for analysis . Finally, 105 patients were recruited for a recent exercise in PD study; however, the intervention was a minimally supervised exercise program . There have been an additional 26 studies published since 2012 investigating exercise in PD, with an average recruitment of 40 participants per study,  making our studies in the high end of what has been reported in the past.
A focus on the infrastructure of the research program, experience of the study team, and ease of participation for the individuals were key players in the success of this PD exercise RCT. Several features of the study design also enhanced the ability of the study team to recruit. Although the strategies described here may not be feasible within all movement disorder programs, it is possible that some or all of them could be adopted or adapted accordingly.
We sincerely thank our patient participants and work of our research team: Alyce Negron and Lucia Blasucci. This work was supported by the following: NS082416 (DH), NS074343(MS, DC), and the National Parkinson Foundation.
SPARX Study Group: B Berman, CL Christiansen, B Kluger, WM Kohrt, Ed Melanson, M Schenkman: University of Colorado Anschutz Medical Campus; CG Moore: Carolinas Healthcare System; DM Corcos, C Poon: Northwestern University; A Delitto, DA Josbeno, S Jain*: University of Pittsburgh; JA Robichaud: University of Illinois Chicago.
Dr. Hall has received research support from NINDS, Parkinson Foundation, Anti-Aging Foundation, Shapiro Foundation, Pfizer, and Abbvie.
She reports no conflicts of interest related to this manuscript.
Dr. Comella has received research funding from NINDS, grants from Allergan Inc., grants and personal fees from Iosen Biopharmaceiticals, grants and personal fees from Merz pharmaceutical, grants from Biotie, grants and personal fees from Revance Therapeutic, personal fees from Acorda Therapeutics, personal fees from Lundbeck Ltd., personal fees from Medtronic, personal fees from Acadia Pharmaceuticals, personal fees from Neurocrine Biosciences Inc., personal fees from Ultragenyx, other from Cambridge Humana Press, other from Wolters Kluwer, grants from URDR, and grants from Dystonia Medical Research Foundation.
Dr. Berman reports grants from National Institutes of Health, during the conduct of the study; grants from NIH/NCATS Colorado CTSI Grant Number KL2 TR001080.
Dr. Kluger has received support from NINDS, NIA, NINR, the Michael J Fox Foundation, the Parkinson Foundation, PCORI, the Colorado Clinical and Translational Sciences Institute, and the Davis Phinney Foundation.
Drs. Corcos, Delitto, Kohrt, Melanson, Moore, Poon, Robichaud, Schenkman, and Ms. Josbeno have received funding from the NIH.
Dr. Christiansen has no disclosures.
Availability of data and materials
The data supporting the conclusions of this article are summarized in the primary outcome paper cited Schenkman et al., 2018 and are physically located at the data coordinating center under the care of Dr. Charity Moore.
DAH and CC are responsible for drafting and editing the manuscript, CM provided the statistical support, and the SPARX study group edited the final manuscript. All authors were involved in the conduct of the exercise clinical trial. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The exercise RCT was approved at each participating institutions IRB – University of Colorado, University of Pittsburgh, and Rush University.
Consent for publication
All authors give consent for publication.
The authors declare that they have no competing interests.
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