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Music to improve sleep quality in adults with depression-related insomnia (MUSTAFI): study protocol for a randomized controlled trial
Trials volume 21, Article number: 305 (2020)
Insomnia is a common sleep disorder for adults with depression, with major impact on their quality of life. Previous trials suggest that listening to music may be helpful in the treatment of sleep disturbances in healthy populations, including students and elderly. In addition, small studies with clinical populations of traumatized refugees, adults with chronic insomnia and adults with depression insomnia add to the evidence base. However, the impact of music listening in the treatment of depression related insomnia is not well documented.
To examine the efficacy of music listening on sleep quality, symptoms of depression, and quality of life in adults with depression-related insomnia.
A single-center randomized controlled trial (RCT) in a two-arm parallel-group design is conducted and reported according to the CONSORT guidelines. The trial consists of an experimental group and a standard care control group. Both groups receive standard treatment for depression following Danish clinical guidelines in an outpatient psychiatry unit. The experimental group listens to music for a minimum of 30 minutes at bedtime for 4 weeks.
This trial will provide information on the efficacy of music intervention as a non-pharmacological intervention in the treatment of depression-related insomnia. This study will provide novel knowledge concerning music medicine as an evidence-based treatment for depression.
Clinicaltrials.gov. ID NCT03676491, registered on 19 September 2018.
Depression is a common health problem and an increasing global burden. WHO has found unipolar depression to be the third largest burden of disease globally in 2004 and is projected to rank first in 2030 . A result of depression is the loss of social and cognitive functions and quality of life. One of the symptoms in depression is reduction in sleep quality (insomnia). Sleep disturbances associated with depression include difficulties in falling asleep and maintaining sleep. Cognitive behavioral therapy (CBT) is recommended in clinical guidelines as first-line treatment [2, 3]. Other treatment modalities for sleep promotion include sleep hygiene, physical activity, light therapy, relaxation techniques, music/nature sounds and acupuncture . Resolving sleep disturbances in patients with active or previous depression is important as it may prevent worsening of symptoms and relapse of depression .
Music listening is widely used as a sleep aid . This practice is supported by a recent Cochrane review concluding that music may be helpful in improving sleep quality in insomnia [5, 6]. The review underlines that the small sample sizes of the studies performed so far is a major limitation and concludes that there is a need for additional intervention studies concerning the effect of music listening on insomnia on specific populations, including patients with depression.
Moreover, a systematic review shows that music listening may reduce symptoms of depression in adults when the music listening is conducted regularly for more than 3 weeks . It was reported that patients responded more when given a choice of music .
Giving a choice of music and offering a selection of music with a variety to meet individual preferences are both important factors highlighted in research [8, 9]. New research should offer a broad selection of calm music to meet these criteria .
Patient-selected music has a risk of being too stimulating (effect-evoking or too dynamic, i.e. increasing pulse and respiratory rate) . Therefore, playlists designed purposefully by music therapists are more likely to have a sleep-inducing effect .
Music preference and culture have an influence on the music-listening experience. The perceived quality of the music depends on age, gender, preference, musical training, and cultural belonging . Music listening is a complex experience that influences the individual in many ways, not strictly in relation to sleep and relaxation, but also in relation to wellbeing and sense of self . An improved sense of wellbeing may positively affect the subjective feeling of restedness. The association between wellbeing and quality of sleep is known and reported in the literature .
This study aims to add knowledge into these domains, investigating wellbeing by quality-of-life questionnaires as well as subjective and objective measures of sleep quality.
We have carried out an observational feasibility study introducing music listening as a non-pharmacological intervention to improve sleep quality for patients with depression . Outpatients diagnosed with unipolar depression and sleeping problems (n = 11) were asked to listen to music for at least 30 minutes before going to sleep every night for a period of 4 weeks. Music listening was provided by a sound pillow equipped with an mp3 player containing 10 playlists of 30–60 minutes of relaxing music with different music styles (classical, easy listening, pop, rock) based on the literature of receptive music therapy . The study indicated signs of improved sleep quality . However, the study lacked a control group.
Rationale for a randomized trial
Effective treatment modalities are in demand to supplement existing treatment of insomnia in depression. The positive effect of music on sleep quality has been reported in a number of study settings with clinical and nonclinical populations . This study contributes to the investigation of the efficacy of music listening in the treatment of depression-related insomnia by combining subjective measures (self-reported data) and objective measures (accelerometer). In addition, a new app with specially designed playlists makes a large selection of music available to meet individual preferences.
Method – aim and hypothesis
The primary aim is to investigate the effect of music listening on sleep quality at 4 weeks follow-up. The secondary aim is to examine whether music listening is effective in reducing symptoms of depression and improving quality of life as well as improving sleep quality at 8 weeks follow-up in patients with depression-related insomnia.
The following hypothesis is tested
Music listening, music intervention, and music medicine refer to the use of music as an intervention without an active music therapist. In this protocol, music listening implies listening to pre-recorded music.
Insomnia, sleep disturbances and sleeping problems refer to a broad understanding of the disorder. Symptoms include difficulties initiating and maintaining sleep.
The study is named MUsic STAr For Insomnia (MUSTAFI).
A single-center randomized controlled trial in a two-arm parallel-group design is conducted from May 2018 to December 2019 following the revised Consolidated Standards of Reporting Trials (CONSORT) guidelines . The RCT includes two groups of participants, an experimental group and a waitlist control group. Both groups receive standard treatment for depression following national guidelines.
The duration of the intervention is 4 weeks. The participants are followed for 8 weeks. Participation takes place in the home of the patient. In addition, three scheduled visits to the hospital in relation to the research project are required. Baseline assessment is performed on the starting day. Follow-up measurements are performed after 4 and 8 weeks (Fig. 3).
The black element in the bottom left of Fig. 3 illustrates the intervention given as an option to the waitlist control group. The participants may take home the sound equipment for 4 weeks. There is no data collection involved. This has been added to the study for ethical reasons and to limit drop out from the control group . The schedule for the trial is described in the SPIRIT flow chart (Fig. 4) and the dimensions of the study protocol have been described, adhering to the SPIRIT checklist (Additional File 1).
Based on a previous study, we assume that the mean decrease in Pittsburgh Sleep Quality Index (PSQI) scale is 3.04 (SD 2) points for the music intervention group and 2.04 (SD 1.67) points for the waitlist control group after 4 weeks of follow-up . When estimating the sample size, we assume that 25% of the eligible patients will be willing to participate in the project. Based on the patient flow in the outpatient clinic and the available resources from the staff recruiting the patients, we assume that a total of 120 participants can be recruited over a period of 18 months. A dropout rate of 20% is expected. Hence, a total of 100 randomized patients are expected to complete the study. Based on the Satterwaite’s two-sample t test and with a total of 100 patients (n = 50 per group) the power of our study is estimated to be 76% (at a confidence level of 5%).
Setting and participants
The study will be conducted at a single study site: the Unit for Depression in Psychiatry at Aalborg University Hospital, Denmark. The participants are adult outpatients aged 18–65 years in treatment for unipolar depression in the Northern part of Denmark.
Patients are referred to the unit for depression with different backgrounds. Some patients have not previously been associated with psychiatry and are referred directly from private practice with moderate or severe symptoms of depression. Another group of patients are referred from an inpatient unit. These patients are in recovery and have a stabilized condition in need of follow-up treatment after discharge. A third group of patients have been diagnosed in previous contact or hospitalization and in need for treatment after a recurrent depression.
All patients are required to have a diagnosis of unipolar depression (ICD-10 Depressive singular episode F32 or Periodic depression F33) and sleeping problems identified by the Hamilton Depression Rating Scale (HAM-D) by a score of at least 2 of a single item or at least 3 in total for the three items (sleep items 4–6). In addition, the patients should receive treatment according to national guidelines for depression. This may include pharmacological treatment, psychotherapy, psycho education and electroconvulsive therapy. Participants are eligible if within age 18–65, in stabilized pharmacological treatment, and having at least 4 weeks of treatment.
Exclusion criteria are unipolar depression with psychotic episodes, substance or alcohol abuse, or sentence to treatment by law. Patients will be excluded if they have restless legs syndrome, obstructive sleep apnea, or other organic sleep disorders as well as hearing loss. In addition, patients with a dislike of music will be excluded.
Patients are recruited in the Unit for Depression. Nurses, psychiatrists, and psychologists use the screening tool 4 weeks after the beginning of treatment or after medical treatment is stabilized. Participants are recruited through posters, information by doctors and word of mouth in the unit. After an initial assessment for eligibility, the patient is informed of the option to participate. The recruitment takes place during group meetings or during individual consultation in the unit. When the patient has declared an interest to participate, the psychiatrist of the patient fill out an inclusion document based on information from the patient journal and his/her knowledge of the patient. The document is forwarded to the research leader. If the patient is eligible, the music therapist makes an appointment to give detailed information on participation in the research project.
Patients are included according to the inclusion and exclusion criteria. The patient may be discharged during participation in the research project and finalize as a private person. If the increase in depression symptoms results in hospitalization, the patient may continue participation in agreement with caretakers in the unit. If the patient is changing medication but is interested in participation, the patient will be registered on a waitlist for inclusion.
The patient may sign the informed consent after receiving oral and written information about the research project. The information explains the aim and the procedures of the research project, the use of sound equipment and accelerometer and the rights as a participant in a scientific health study. The patient has the option to ask questions and if the patient need time to consider the participation, the music therapist offer to call the patient after 1 week and a new meeting is set up for the signing of the informed consent. When the informed consent is obtained and the inclusion criteria are confirmed in the inclusion document, the music therapist proceeds with the randomization. An additional consent for collection and use of log file data from accelerometer and the Music Star app is signed after randomization. Documents of informed consent are kept in a securely locked place.
Randomization takes place when the inclusion document has confirmed eligibility and the informed consent has been signed following the regulations of the The North Denmark Region Committee on Health Research Ethics Randomization is carried out by the use of REDCap (Research Electronic Data Capture) hosted at Aalborg University Hospital. REDCap is a secure web-based application designed to support data capture for research studies. The randomization will be stratified according to age, i.e., under 30 years versus 30 years and above. Randomization is performed using computer-generated block randomization (random block sizes 2–8) with 1:1 allocation between the intervention group and the waitlist control group.
The principal investigator is assigned to give information on the research project to groups and individuals by team members and coming to the unit by appointment. When offering thorough information to obtain informed consent, the music therapist takes the participant to the music therapy clinic situated in a hospital building close by.
The music intervention consists of listening to music with the use of a sound pillow, applying the music from the Music Star app with special designed playlists. The duration of music listening for 30 minutes minimum at bedtime is guided by previous studies . The principal investigator HNL gives an oral guideline to music listening and use of sound equipment at the baseline appointment including how to adjust the volume. The pillow speakers allow audio listening at very low volume. Adherence to the intervention (30 minutes of bedtime music) is monitored through log file data from The Music Star app.
Instructions for the experimental intervention:
It is required that you listen to music of your choice from the Music Star for at least 30 minutes at bedtime every night for 4 weeks. You may use the Music Star during the night or in the early hours of the morning if you wake up and have difficulty falling asleep again.
You may turn off the Music Star if you wake up when the music plays and it is disturbing.
The music will automatically stop when the playlist ends after 30 or 60 minutes.
You may use the Music Star in the daytime to assist a rest. It is important only to use the Music Star for relaxation and sleep.
You are advised to listen to the different music available to select your preferred playlists. You may select a particular playlist to play every night. Some people find that it is helpful to let a specific piece of music be a signal for sleep initiation.
Consider choosing music that you like and that may help you fall asleep.
You have to listen to music at night in the way it is described for the research purpose, i.e. the sound pillow in combination with the Music Star app.
You may listen to your own music during the daytime.
Instructions on the use of the sound equipment:
Place the sound pillow on your bed (remove your own pillow) and place the Music Star close to the bed on a small table or chair for easy access during the night.
Make sure that you have recharged the Music Star during the day.
If you have technical problems with the sound equipment, you may contact the research leader by phone from 9am to 12pm on weekdays.
Waitlist control group
The participants in the waitlist control group are asked to continue their normal bedtime routines. They are not given any instructions concerning music listening during the 8 weeks. At the baseline appointment, they are informed of the option to take home the music equipment to test for 4 weeks at the end of the 8-week period.
The data are derived from four questionnaires (three are self-reported and one is scored by the psychiatrist, researcher, or project nurse) and log file data from the accelerometer and from the Music Star app. The references concerning validation of each instrument below are selected according to their relevance to this study.
The Pittsburgh Sleep Quality Index (PSQI)
Is a commonly used questionnaire measuring self-reported sleep habits in clinical populations in research and clinical practice . A Danish version of the questionnaire will be used. The items refer to sleep habits and disturbances within the last month. The 19 items are divided in seven domains: subjective sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbances, daytime dysfunctions and use of antidepressant agents. The seven components form a global score ranging from 0 to 21, each component with a range from 0 to 3. Buysse et al. reported a score of > 5 (indicating poor sleep) yielded a diagnostic sensitivity of 89.6% and a specificity of 86.5% . The scale shows good homogeneity with an internal consistency, with α = 0.83. Acceptable measures of validity were obtained through the ability to distinguish between clinically distinct groups and comparing these with polysomnographic results. A score of > 5 is indicative of severe sleep difficulties in at least two areas, and separating participants in two categories “good” and “poor”. PSQI is validated in psychiatric populations .
The Hamilton Depression Scale (HAM-D17)
The HAM-D17 consists of 17 items . The items cover the depressive state, the unspecific stress and arousal symptoms, the suicidal thoughts, and lack of insight. The respondent is asked to consider the last 3 days when responding.
Each item in the score is rated from 0 to 4 or 0 to 2, the higher number indication an increase in the symptoms of depression. A guide to the Hamilton rating questioning is used in combination with a rating sheet. The total score indicates the severity of depression symptoms graduating in four categories from unlikely depression to severe depression, with 8–12 indicating minimal depression, 13–17 indicating light depression, 18–24 indicating moderate depression, and 25–52 indicating severe depression.
The 17-item version of the Hamilton Depression Rating Scale is validated .
The 5-item World Health Organization Well-Being Index (WHO-5)
The 5-item World Health Organization Well-Being Index (WHO-5) is among the most widely used questionnaires assessing subjective psychological well-being . It measures subjective quality of life based on positive mood (good spirits, relaxation), vitality (being active and waking up fresh and rested), and general interest (being interested in things). WHO-5 only contains positively phrased items. The WHO-5 items are: (1) ‘I have felt cheerful and in good spirits’, (2) ‘I have felt calm and relaxed’, (3) ‘I have felt active and vigorous’, (4) ‘I woke up feeling fresh and rested’, and (5) ‘My daily life has been filled with things that interest me’. The respondent is asked to rate how well each of the five statements applies to him or her when considering the last 14 days. Each of the five items is scored from 5 (all of the time) to 0 (none of the time). The score therefore theoretically ranges from zero (absence of well-being) to 25 (maximal well-being). The use of WHO-5 as a measure of severity of depression is validated [24).
The World Health Organization Quality of Life BREF (WHOQOL-BREF)
In 1991, the World Health Organization initiated a project with the aim of developing an international, cross-culturally comparable QOL assessment instrument. “It assesses the individual’s perceptions in the context of their culture and value systems, and their personal goals, standards and concerns. The WHOQOL instruments were developed collaboratively in a number of centres worldwide, and have been widely field-tested.” . The WHOQOL-BREF instrument is a shorter version of the original 100-item self-report questionnaire, comprising 26 items measuring four domains: physical health, psychological health, social relationships, and environment. In each question, the respondent reports his/her QOL in the four domains on a 5-point Likert scale. A high score reflects the subjective experience of high QOL. The use of WHO-QOL-BREF is validated .
The Music Star app
An app designed for iPad in 2014. The Music Star is a self-explanatory user interface to select music from specifically designed playlists. Music therapists have selected the music for the playlists. The app has a built-in log function that registers each event when using the app. The Music Star gives information from log files of music played, time, and duration .
The 16 playlists of 30–60 minutes duration are represented by colored triangles forming a star. The four playlists in shades of blue are the most quiet and simple (lowest stimuli), the four playlists in shades of green include some variation and dynamics (moderate stimuli), the four playlists in shades of red have more intensity (highest stimuli). The grey triangles are intended to contain playlists for specific purposes. A grey triangle contains the only non-music playlist of ‘Summer Rain’ consisting of sounds of rain and bird sounds. The rain sound adds a non-music track for the purpose of variety in sound stimuli to meet individual preferences. Two other grey triangles contain special designed playlists for sleep. The classification of music is correlated to the degree of complexity and tension of the musical stimulus based on the taxonomy of music by Wärje & Bonde . The playlists in The Music Star are all categorized in subdivisions of supportive music according to the taxonomy of music. The two sleep playlists have a 30- minute duration. Sleep 1 is a short version of a playlist with music specially composed for relaxation and sleep, including a male voice humming. Sleep 2 is a playlist with a guitar-bass jazz duo playing slow ballads. Sleep 1 and 2 are included for meeting criteria of minimum duration and variety in the music selection. More than 100 music pieces in different genres are available in the playlists.
One triaxial accelerometer with on board memory (Axivity Ax3, Newcastle upon Tyne, UK) placed in a wrist bracelet will be used to measure arm movement during the night. The measurement range was set to ± 8G with a sampling frequency of 25 Hz. A sleep analysis function using a generic algorithm will provide data on sleep duration. Assessing sleep duration with an accelerometer is validated .
Primary outcome measure
We assess subjective quality of sleep through patient self-reports using the PSQI to obtain data on psychological and emotional well-being.
The primary endpoint is defined as change of subjective sleep quality from baseline at 4 weeks. Treatment benefit is achieved when the PSQI score is decreased with statistical significant change after the 4-week intervention period.
Secondary outcome measures
We assess sleep quality using actigraphy to obtain objective sleep data. We assess symptoms of depression using HAM-D17 to obtain data on the depressive state. Finally, we assess quality of life using WHO-5 and WHOQOL-BREF to obtain data on psychological well-being considering mood, vitality, and interests (WHO-5) and physical/psychological health, social engagement, and environment (WHOQOL-BREF).
The secondary outcome measures are selected to address these objectives (secondary outcome measure 2, 4, 6, and 8). Measuring change from baseline at 8 weeks, assess sustainability of results, and progression of symptoms over time (secondary outcome measure 1,3,5,7, and 9).
The nine secondary endpoints are defined and listed below:
Subjective sleep quality (PSQI): Change of sleep quality from baseline at 8 weeks
Objective sleep quality (Actigraphy): Change of sleep quality from baseline at 4 weeks
Objective sleep quality (Actigraphy): Change of sleep quality from baseline at 8 weeks
Symptoms of depression (HAM-D17): Change of depression level from baseline at 4 weeks
Symptoms of depression (HAM-D17): Change of depression level from baseline at 8 weeks
Quality of life (WHO-5): Change of quality of life from baseline at 4 weeks
Quality of life (WHO-5): Change of quality of life from baseline at 8 weeks
Quality of life (WHOQOL-BREF): Change of quality of life from baseline at 4 weeks
Quality of life (WHOQOL-BREF): Change of quality of life from baseline at 8 weeks
All outcome measures are collected at baseline, after 4 weeks experimental/wait-list control and again after 4 weeks of follow-up. In addition, registration of pharmacological treatment during the period of participation is included in the data collection.
At baseline, demographic information including age, sex, ethnicity, and partnership, children living at home, handedness, diagnosis code for present depression, first diagnosis of depression, and first psychiatric diagnosis will be gathered. In addition, the participant may add self-reported other disease and/or diagnosis. Work status and education, alcohol use, and habitual use of music for sleep will be registered.
We initially perform a descriptive analysis on age, gender, medication, illness duration etc. The two groups are compared within groups and between groups using F-tests and chi-squared tests. Additionally, we compare the groups on outcome measures at baseline.
Data analysis for the RCT will be performed using mixed effects linear regression with subject specific random effects. The intervention group will be initially compared with the control group on change of all outcome measures after 4 and 8 weeks. Age and gender will be added as covariates in all regression analyses. Repeated-measures analysis of variance (RM-ANOVA) will be used to compare results from baseline follow-up one and follow-up two.
Finally, a descriptive analysis of the playlists is included in the study, i.e. analysis of playlist preferences (style, duration, time of day) in the group of patients benefitting most from treatment compared to the group of patients benefitting the least.
Blinding of the researchers performing the scorings before and after the treatment as well as the subjects of the study will not be possible. Patients will be anonymized when analyzing data. All main analyses will be carried out based on the intention-to-treat principle. Information on adherence is obtained from the Music Star log file data. Compliance rate will be part of the primary study publication.
In case treatment is associated with dropout rate, we will investigate differences in baseline characteristics between complete cases and patients that are lost to follow-up. Any baseline characteristics that are significantly different between these two groups will be used as adjustment parameters in a sensitivity analysis of music listening treatment on the primary outcome.
A multiple comparisons analysis will not be performed, since the results of the analyses of music listening treatment on secondary outcome are purely exploratory, in which case multiple testing analysis is less important .
Data collection and management
Data collection consists of several elements. The PSQI, WHO-5, and WHOQOL-BREF are questionnaires filled out exclusively by the participants. The HAM-D rating is performed by the researcher (HNL). Data management is carried out by the use of REDCap. Double data entry is performed by research assistants.
The study is approved by the local ethics committee (N-20170055) and registered by the Danish Data Protection Agency (ID 2017–236). A yearly report of adverse events and other unintended effects of the trial will be obtained by the local ethics committee.
Results of the study will be published in open-access peer-reviewed scientific journals and presented at international scientific conferences regardless of the conclusion. Broadcast of findings on Danish radio and TV media will be planned through the study.
The aim of this RCT is to investigate the efficacy of music medicine compared with standard care. In order to increase the clinical value of the research, the inclusion and exclusion criteria have been selected to target a group of depressive patients who have serious sleep disturbances. This group of patients is less likely to respond to interventions such as cognitive behavioral therapy. Further, there is an augmented risk of relapse and suicide [27, 28]. Sleep disturbances in depression result in a slowdown of the recovery process for the individual and this is costly for the individual and for the society .
If music medicine using the Music Star app combined with a sound pillow shows to be effective in improving sleep, it may not only have a positive effect on sleeplessness but also promote compliance with treatment and increase overall functioning .
The primary outcome measure is self-reported sleep. Negative thinking is a symptom in depression that may influence self-rating. The HAM-D17 rating is not performed consistently by one person in all cases. Inter-rater reliability has not been tested and may cause bias.
This study does not consider issues of comorbidity. For some patients, sleep disturbances have been present long before the onset of depression. In this study, sleep disturbances are associated with depression although the comorbid presentation of depression and insomnia may be complex. The analysis of secondary outcomes is exploratory and thus more studies will be needed to confirm the results.
Recruitment will take place from 23 May, 2018 to the end of February 2020. By May 2019, 42 participants had been included in the study. The current protocol is version 3, dated 17 October, 2018.
Availability of data and materials
The data sets used during the current study are available from the corresponding author on reasonable request.
Hamilton Depression Rating Scale
Pittsburg Sleep Quality Index
World Health Organization-Five Well-Being Index
World Health Organization Quality of Life BREF questionnaire
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We thank Lars Ole Bonde for assistance adjusting the study design and Lars Rye Bertelsen for setting up software and data collection for the Music Star. We thank Maria Rodrigo Domingo for statistical assistance, Simon Grøntved for setting up software (REDCAP) and Mette Munk for administrative assistance. We thank the patients who gave their consent to participate.
The study is funded by Clinic South, Aalborg University Hospital - Psychiatry, The Obel Family Foundation, Aase and Ejnar Danielsens Foundation, and The Danish North Region Health Research Foundation. We thank the funding bodies for their vital financial support. The funding bodies have no role or authority over any part of the research or publication of the trial.
Ethics approval and consent to participate
The study was approved by the North Denmark Region Committee on Health Research Ethics on 5 September 2017; N-20170055 case number 58691. Additional applications have been approved 15 March, 2018 and 17 October, 2018 case number 62478. Protocol version number 3. Participants sign an informed consent to participate. Additional consent for collection and use of log data from the accelerometer and the Music Star app has been signed by all participants.
Consent for publication
HNL is co-inventor of the Music Star app and has economic interest in the research due to ownership and sales of the Music Star app. The Music Star app is commercialized in collaboration with the company AudioCura, which delivers sound equipment to Aalborg University Hospital. The company has no influence on the study. The inventors HNL and LRB are music therapists employed at Aalborg University Hospital of whom only HNL (the first author) is a member of the research group. The inventors follow the ethical principles by the Danish Union of Music Therapists (Dansk Musikterapeutforening). HNL is responsible for data collection. All data are entered in REDCAP by a research assistant independently of the first author. A statistician is responsible for data analysis. The authors INP, SPJ, AMH-S, MT, GB, JIL, EK, AL, HØ, BG, HB, JBV, and JM declare that they have no competing interests.
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Lund, H.N., Pedersen, I.N., Johnsen, S.P. et al. Music to improve sleep quality in adults with depression-related insomnia (MUSTAFI): study protocol for a randomized controlled trial. Trials 21, 305 (2020). https://doi.org/10.1186/s13063-020-04247-9