Community Choirs To Promote Healthy Aging; Community of Voices Chorus

Not Applicable

Completed

• Conditions: Well Being
• Interventions: Behavioral: Community of Voices choir program; Behavioral: Wait-list control group

• Registration Number: NCT01869179
• Lead Sponsor: University of California, San Francisco

Brief Summary

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:

1. 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.

2. 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2013-01-09
• Study Start: 2013-02
• Study First Submitted QC: 2013-05-30
• Study First Posted: 2013-06-05
• Primary Completion: 2016-12-01
• Study Completion: 2018-08-01
• Status Verified: 2020-01
• Last Update Submitted: 2020-01-13
• Last Update Posted: 2020-01-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 390

Inclusion Criteria

• Age 60 and older
• Living independently
• Have adequate visual and auditory acuity (with correction) to complete testing
• Speak English or Spanish (including both bilingual and monolingual Spanish speakers)

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Exclusion Criteria

• A baseline diagnosis of dementia, determined by the screening tool or self-report of diagnosis
• Have an unstable or serious medical condition that would limit participation in the weekly choir sessions or assessments, including current (but not prior) severe psychiatric disorder
• Currently singing in a choir, within the last 6 months
• Plans to move out of the area within 12 months

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Wait-list control group	Community of Voices choir program	Waits six months, and at the end of the six months is offered the option of participating in the 12 month choir program.
Wait-list control group	Wait-list control group	Waits six months, and at the end of the six months is offered the option of participating in the 12 month choir program.
Community of Voices choir program	Community of Voices choir program	Participants will receive the 12 month choir program as soon as possible after study enrollment.

Primary Outcome Measures

Name	Time	Method
Physical function	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	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	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.

Secondary Outcome Measures

Name	Time	Method
Health Care Services Utilization	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	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
Health-Related Quality of Life	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
Shortness of breath	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	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.
Emotion	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.
Memory and Executive Function	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.

Trial Locations

Locations (1)

UCSF Institute for Health & Aging; 🇺🇸 San Francisco, California, United States