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End Stage Renal DiseaseNCT03925168

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

A study testing Music therapy in people with End Stage Renal Disease and Depression, run by Tulane University at 3 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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 more about this study

Who is it for?
Ages 21 years and older
Conditions the study is for
End Stage Renal Disease, Depression, Anxiety
What is being tested?
Music therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
3 sitesUnited States
Study dates
8 Mar 2019to 1 Jan 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • do not speak English, deafness

Trial locations and contacts

3 sites in 1 country.

United States3 sites
  • DCI Canal Street

    New Orleans, Louisiana, 70112

  • Tulane University School of Medicine

    New Orleans, Louisiana, 70112

  • DCI West Bank

    Terrytown, Louisiana, 70056

Other trials in United States

About this study

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.

Being tested
Music therapy
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
Medical subject headings
Kidney Failure, Chronic, Depression, Anxiety Disorders, Depressive Disorder, Major, Generalized Anxiety Disorder, Patient Compliance, Medication Adherence, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Music therapyBehavioural

    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.

Study groups in NCT03925168
Study groupRoleWhat they receive
ExperimentalExperimentalMusic therapy
Receives: Behavioral: Music therapy
ControlNo interventionNo music therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 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.

    Measured: 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.

    Measured: Until 90 days post study

  4. Compliance with dialysis

    Self-reported

    Measured: Up to 5 months

  5. Number of hospitalizations

    Self-reported

    Measured: Up to 5 months

Secondary outcomes (6)
  1. Blood pressure

    Measured: Up to 5 months

  2. Heart rate

    Measured: 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.

    Measured: 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.

    Measured: 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.

    Measured: 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.

    Measured: Up to 5 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Apr 2019
  2. Study start8 Mar 2019
  3. Primary completion1 Jan 2020
  4. Study completion1 Jan 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Cluster-randomized clinical trial
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03925168
Sponsor's protocol ID
2017-866
Status last verified
Jan 2021
First submitted
16 Apr 2019
Last updated
15 Jan 2021
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Music therapy in people with End Stage Renal Disease and Depression, run by Tulane University at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Jan 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Depression (time frame: Until 90 days post study). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jan 2021.

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