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

Primary Purpose

End Stage Renal Disease, Depression, Anxiety

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Music therapy
Sponsored by
Tulane University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Disease focused on measuring 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

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  • do not speak English, deafness

Sites / Locations

  • DCI Canal Street
  • Tulane University School of Medicine
  • DCI West Bank

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental

Control

Arm Description

Music therapy

No music therapy

Outcomes

Primary Outcome Measures

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.
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.
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.
Compliance with dialysis
Self-reported
Number of hospitalizations
Self-reported

Secondary Outcome Measures

Blood pressure
Heart rate
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.
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.
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.
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.

Full Information

First Posted
April 16, 2019
Last Updated
January 13, 2021
Sponsor
Tulane University
Collaborators
National Kidney Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03925168
Brief Title
Music Therapy and Dialysis: A Pilot Investigation Into the Effectiveness of Patient-Selected Music Interventions on Physiological, Psychological, and Quality-of-Life Outcomes
Official Title
Music Therapy and Dialysis: A Pilot Investigation Into the Effectiveness of Patient-Selected Music Interventions on Physiological, Psychological, and Quality-of-Life Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
March 8, 2019 (Actual)
Primary Completion Date
January 1, 2020 (Actual)
Study Completion Date
January 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tulane University
Collaborators
National Kidney Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster-randomized clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental
Arm Type
Experimental
Arm Description
Music therapy
Arm Title
Control
Arm Type
No Intervention
Arm Description
No music therapy
Intervention Type
Behavioral
Intervention Name(s)
Music therapy
Intervention Description
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.
Primary Outcome Measure Information:
Title
Depression
Description
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
Title
Anxiety
Description
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
Title
Measuring change in Quality of life using Kidney Disease and Quality of Life 36 patient screening tool (KDQOL36)
Description
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
Title
Compliance with dialysis
Description
Self-reported
Time Frame
Up to 5 months
Title
Number of hospitalizations
Description
Self-reported
Time Frame
Up to 5 months
Secondary Outcome Measure Information:
Title
Blood pressure
Time Frame
Up to 5 months
Title
Heart rate
Time Frame
Up to 5 months
Title
Medication compliance questionnaire.
Description
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
Title
Measure change in Pain using the Numeric Rating Scale 11 (NRS11)
Description
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
Title
Participant Energy
Description
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
Title
Mood
Description
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English-speaking, adult (21+) hemodialysis patients who receive dialysis at the one of the two outpatient dialysis centers Exclusion Criteria: do not speak English, deafness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angelina Dixon, MD
Organizational Affiliation
Tulane University
Official's Role
Principal Investigator
Facility Information:
Facility Name
DCI Canal Street
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
Tulane University School of Medicine
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
DCI West Bank
City
Terrytown
State/Province
Louisiana
ZIP/Postal Code
70056
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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