Community Choirs To Promote Healthy Aging; Community of Voices Chorus
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|ClinicalTrials.gov Identifier: NCT01869179|
Recruitment Status : Unknown
Verified January 2015 by University of California, San Francisco.
Recruitment status was: Recruiting
First Posted : June 5, 2013
Last Update Posted : January 15, 2015
The investigators will recruit 450 older adults and will utilize 12 Administration on Aging (AoA)-supported senior centers to implement a multisite, cluster randomized (by center), wait-list clinical trial. Centers will be randomized to receive the choir program immediately (intervention group) or after a 6-month delayed intervention phase (control group). The community choirs will be led by professional music directors. The investigators will assess both primary and secondary outcomes at baseline, 6 and 12 months, with the main intervention group comparison being at 6 months. The investigators will also evaluate the start-up and ongoing program costs for senior centers, including cost/person served and determine quality adjusted life years.
The hypotheses are:
- Compared to delayed intervention controls, participation in a community choir program will be associated with improvements/maintenance on the primary outcomes of physical function (balance, walking speed, strength), depressive symptoms, and cognition (executive function and memory) at 6 months. The investigators also predict within-group improvements on these primary outcomes at 12 months.
- Compared to delayed intervention controls, participation in a community choir program will be associated with improvements in the secondary outcomes of well-being (depressive symptoms, loneliness, resilience, social participation, health-related quality of life, shortness of breath, functional status, falls, and health services use) at 6 months. The investigators also predict within-group improvements on these secondary outcomes at 12 months.
|Condition or disease||Intervention/treatment||Phase|
|Well Being||Behavioral: Choir program||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||450 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Community Choirs To Promote Healthy Aging And Independence Of Older Adults|
|Study Start Date :||February 2013|
|Estimated Primary Completion Date :||September 2015|
|Estimated Study Completion Date :||September 2016|
Experimental: Choir program
Participants will receive the 12 month choir program as soon as possible after study enrollment.
Behavioral: Choir program
Attend weekly choir sessions for 12 months at the Senior Center. Choir sessions will last about 90 minutes each with a 20 minute break. Take part in 3 informal choir concerts.
No Intervention: Wait-list Control
Waits six months, and at the end of the six months is offered the option of participating in the 12 month choir program.
- Physical function [ Time Frame: up to 12 months ]We will measure several physical function outcomes. The Short Physical Performance Battery (SPPB) chair stands will be the primary outcome measure. Baseline, 6 months, 12 months. Additional motor function outcomes using the NIH Toolbox are listed below.
- Cognitive Function [ Time Frame: up to 12 months ]We will use the Trailmaking Test as a primary outcome of executive function. Baseline, 6 months, 12 months. Additional tests of executive function and memory are listed as secondary outcomes.
- Depressive Symptoms [ Time Frame: up to 12 months ]We will use the Patient Health Questionnaire (PHQ-8) as a primary measure of depressive symptoms. Baseline, 6 months, 12 months. Additional NIH Toolbox Emotion measures are listed as secondary outcomes.
- Health-Related Quality of Life [ Time Frame: up to 12 months ]We will use the brief, self-report European Quality of Life (EQ-5D) to measure health-related quality of life. It has versions in both English and Spanish and also alternate and phone versions. It covers five dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Baseline, 6 months, 12 months
- Health Care Services Utilization [ Time Frame: up to 12 months ]We will track utilization of health care services for cost analysis. The list of health care services is modified from the Chronic Disease Self-Management study and includes visits to a doctor, mental health provider (e.g., counselor, psychologist), other health providers (e.g., home health nurse, physical therapist), and emergency room and hospitalizations (and reason for stay). Participants (including those on the wait-list) will be contacted by phone every three months to complete the form about health care services used in the prior three months. Baseline, 6 months, 12 months
- Falls [ Time Frame: up to 12 months ]We will query frequency of falls using a single question commonly used in several large diverse studies about falls. Falls will also be assessed by phone every three months. Baseline, 6 months, 12 months
- Shortness of breath [ Time Frame: up to 12 months ]We will ask three questions about shortness of breath based on Blazer and colleagues. Baseline, 6 months, 12 months
- Balance and Endurance [ Time Frame: up to 12 months ]We will use the NIH Toolbox Motor to assess endurance (4 Meter Walk Gait Speed Test) and balance (Standing Balance Test). Baseline, 6 months, 12 months.
- Memory and Executive Function [ Time Frame: up to 12 months ]As secondary cognitive outcomes, we will use the NIH Toolbox to assess executive function and attention (NIH Toolbox Flanker Inhibitory Control and Attention Test) and verbal memory (NIH Toolbox Auditory Verbal Learning Test - Rey). Baseline, 6 months, 12 months.
- Emotion [ Time Frame: up to 12 months ]We will also be using the NIH Toolbox to assess additional aspects of emotion, including psychological well-being (Positive Affect), Self-Efficacy, social relationships (Emotional Support, Friendship, Loneliness), negative affect (Fear-Affect, Sadness), Medical Outcomes Study (MOS) social support, and Apathy. Baseline, 6 months, 12 months.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01869179
|Contact: Rachel Freyre, BS||415-476-5903||Rachel.Freyre@ucsf.edu|
|Contact: Jasmine Santoyo-Olsson, MSemail@example.com|
|United States, California|
|UCSF Institute for Health & Aging||Recruiting|
|San Francisco, California, United States, 94118|
|Principal Investigator:||Julene K Johnson, PhD||University of California, San Francisco|