CClinicalTrials.gg
CompletedNCT03925168Updated Jan 15, 2021

Music Therapy and Dialysis: A Pilot Investigation Into the Effectiveness of Patient-Selected Music Interventions on Physiological, Psychological, and Quality-of-Life Outcomes

An interventional study of Music therapy in End Stage Renal Disease, Depression and Anxiety, sponsored by Tulane University. Completed at 3 sites in United States. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2021-01-15.

Sponsored by Tulane University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
21 Years and older
Sex
All
01

Study summary

The objective of this study is to determine the effect of music therapy during dialysis on:

depression, anxiety, quality of life, blood pressure, heart rate, medication compliance, compliance with dialysis treatment, number of hospitalizations, pain level, and energy level.

Read the detailed description

This study will be a cluster-randomized clinical trial. In order to limit contamination bias, dialysis sessions at each site will be randomized to the experimental group or the wait-list control group. For example, patients receiving MWF first-session dialysis may be randomized to the experimental group while patients receiving TTS second-session dialysis may be randomized to the control group. Due to this randomization scheme, patients will be able to receive individualized music therapy while sitting in an open dialysis unit. The subject population includes English-speaking, adult (21+) hemodialysis patients who receive dialysis at the one of the two outpatient dialysis centers included in this study. Subjects will be excluded if they do not speak English or if they are deaf as these patient populations would not be likely to benefit from music therapy administered in English. Up to 100 patients will be enrolled in this study.

Patients receiving dialysis at DCI, Inc, who consent to participate and are randomized to the experimental group will receive 30-minute music therapy sessions over the course of several months. Music therapy will be administered by certified music therapists and music therapy students according to the Eyre (2008) decision tree model. According to this model, the patient chooses his or her preferred musical intervention at the beginning of each session. Choices include: sing songs, compose a song, listen to songs, play instruments, have an imagery experience, listen to music, improvise, and use music for relaxation. If the patient is unwilling or unable to make a decision, then the music therapist will choose an intervention based on the patient's perceived needs. For example, if the perceived need is expression of emotions, then the music therapist may suggest song composition, song choice, song singing, or improvisation. The music therapist will continue to assess the client's perceived needs based on their physical, verbal, and emotional responses to the chosen musical interventions, and the therapist will adjust their musical interventions accordingly (the complete Eyre Decision Tree Model is attached). The instruments utilized in music therapy will include a classic guitar, gato box (a small, drum-like instrument), and a 3-piece egg shaker set. All of these instruments can be played loudly enough to provide music therapy to the patient but softly enough as to not disturb the adjacent patients in the dialysis unit. In fact, these instruments are frequently used to provide music therapy to patients in open neonatal intensive care units.

The primary variables in this study include depression, anxiety, and quality of life. The median time to recovery for a major depressive episode is 20 weeks; therefore, patients randomized to the control group will receive music therapy for approximately 20 weeks. Depression will be measured using the Patient Health Questionnaire-9 (PHQ-9), anxiety will be measured using the Generalized Anxiety Disorder-7 (GAD-7), and quality of life will be measured using the Kidney Disease and Quality of Life (KDQOL™-36) questionnaire. These tools are self-administered questionnaires that will be provided by the music therapists to both the experimental and control groups once a month during the study. Any patient with a PHQ-9 score greater than 10 (moderate depression) or a GAD-7 score greater than 10 (moderate anxiety) will additionally be given resources for available mental health providers in the area. While these tools are validated to be utilized every two weeks, they will be utilized every month during this study to limit testing fatigue. In addition, the PHQ-9, GAD-7, and KDQOL™-36 will be administered 30, 60, and 90 days after the experimental group receives their last music therapy session to both the experimental and control groups to assess for recurrent episodes. Among patients with major depressive disorder, recurrent episodes occur in approximately 50 percent. The risk of reoccurrence appears to be greatest in the first few months after cessation of depressive therapy.

The secondary variables in this study include blood pressure, heart rate, medication compliance, compliance with dialysis treatment, number of hospitalizations, pain level, and energy level. The music therapists will record the heart rate (HR) and blood pressure (BP) of each patient at the beginning of dialysis as well as at the beginning and end of music therapy (or a 30-minute period during which music therapy would have been administered). These HRs and BPs will be recorded using nursing vitals. Prior to the start of each session, the music therapist will provide self-administered questionnaires that ask patients to rate their pain (utilizing the Numeric Rating Scale [NRS-11]), mood, anxiety, and energy level. The patients will rate their pain, mood, anxiety, and energy level at the end of the session as well. The music therapist will record if the patient stayed for their entire treatment, or if they asked to stop dialysis early (the complete weekly and monthly data collection forms are attached). Music therapy sessions will be audio recorded using a condenser microphone and iPad Pro, and any subjective feedback from dialysis patients about music therapy sessions will be recorded as well.

02

Conditions studied

  • End Stage Renal Disease
  • Depression
  • Anxiety
  • Major Depressive Disorder
  • Generalized Anxiety Disorder
  • Compliance, Patient
  • Compliance, Medication
  • Mood
  • Pain
  • Energy Supply; Deficiency
  • Quality of Life
  • Blood Pressure
  • Heart Rate Fast

Keywords

  • end stage kidney disease
  • depression
  • major depressive disorder
  • anxiety
  • generalized anxiety disorder
  • music therapy
  • dialysis
  • quality of life
  • blood pressure
  • heart rate
  • pain
  • energy
  • mood
  • medication compliance
  • music
03

In context

Kidney Failure, Chronic

2,085 studies on the registry are indexed under Kidney Failure, Chronic; 260 are open to participants now.

This study's enrollment of 50 is close to the median of 55 across 1,557 interventional studies indexed under Kidney Failure, Chronic.

Browse Kidney Failure, Chronic studies →

Lead sponsor

Tulane University is the lead sponsor of 98 studies on the registry; 30 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 5 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • English-speaking, adult (21+) hemodialysis patients who receive dialysis at the one of the two outpatient dialysis centers

Exclusion criteria

Exclusion Criteria:

  • do not speak English, deafness
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Experimental

    Music therapy

    Behavioral: Music therapy

  • No intervention
    Control

    No music therapy

Interventions

  • BehavioralMusic therapy

    Music therapy will be administered according to the Eyre (2008) decision tree model. According to this model, the patient chooses his or her preferred musical intervention at the beginning of each session. Choices include: sing songs, compose a song, listen to songs, play instruments, have an imagery experience, listen to music, improvise, and use music for relaxation.

06

What researchers measure

Primary outcomes

  1. Depression

    Measured by Patient Health Questionnaire 9 (PHQ-9). The PHQ-9 measures depression symptoms. Scores range from 0 to 27. A score of 0 to 4 indicates no depression symptoms, 5 to 9 indicates mild symptoms, 10 to 14 indicates moderate symptoms, 15 to 19 indicates moderately severe symptoms, and 20 to 27 indicates severe symptoms.

    Time frame: Until 90 days post study

  2. Anxiety

    Measured by Generalized Anxiety Disorder 7 patient screening tool (GAD-7). The GAD-7 measures anxiety symptoms. Scores range from 0 to 21. A score of 5 or higher indicates mild anxiety, 10 or higher indicates moderate anxiety, and 15 or higher indicates severe anxiety.

    Time frame: Until 90 days post study

  3. Measuring change in Quality of life using Kidney Disease and Quality of Life 36 patient screening tool (KDQOL36)

    Measured by Kidney Disease and Quality of Life 36 patient screening tool. The KDQOL36 measures quality of life for kidney disease patients. Scores range from 36 to 172. Lower scores indicate greater quality of life. Appropriate scores vary by age.

    Time frame: Until 90 days post study

  4. Compliance with dialysis

    Self-reported

    Time frame: Up to 5 months

  5. Number of hospitalizations

    Self-reported

    Time frame: Up to 5 months

Secondary outcomes

  1. Blood pressure

    Time frame: Up to 5 months

  2. Heart rate

    Time frame: Up to 5 months

  3. Medication compliance questionnaire.

    A questionnaire about medication compliance will be administered to patients so that they can self report compliance with medications and compliance with dialysis.

    Time frame: Up to 5 months

  4. Measure change in Pain using the Numeric Rating Scale 11 (NRS11)

    Measured by the Numeric Rating Scale 11. This scale ranges from 0 to 11. A score of 0 indicates no pain while a score of 11 indicates severe pain.

    Time frame: Up to 5 months

  5. Participant Energy

    A questionnaire about energy will be administered to patients so that they can rate their energy on a scale from 0 to 5. A score of 0 indicates no energy while a score of 5 indicates a great amount of energy.

    Time frame: Up to 5 months

  6. Mood

    A questionnaire about mood will be administered to patients so that they can rate their mood on a scale from 0 to 5. A score of 0 indicates poor mood while a score of 5 indicates a great mood.

    Time frame: Up to 5 months

07

Study locations

3 sites
  • DCI Canal Street
    New Orleans, Louisiana 70112, United States
  • Tulane University School of Medicine
    New Orleans, Louisiana 70112, United States
  • DCI West Bank
    Terrytown, Louisiana 70056, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 15, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03925168
Lead sponsor
Tulane University
Collaborators
National Kidney Foundation
Responsible party
Sponsor
First posted
Apr 24, 2019
Start date
Mar 8, 2019
Primary completion
Jan 1, 2020
Completion
Jan 1, 2020
Last update
Jan 15, 2021

Study contacts

Angelina Dixon, MD
principal investigator · Tulane University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion