Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01869179
Other study ID # R01AG042526
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2013
Est. completion date August 1, 2018

Study information

Verified date January 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 390
Est. completion date August 1, 2018
Est. primary completion date December 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility 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)

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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Community of Voices choir program
Attend weekly choir sessions for 12 months at the Senior Center. All choir sessions will include activities that focus on cognitive, psychosocial, and physical engagement components Choir sessions will last 90 minutes each with a 10 minute break. Take part in 3-4 informal choir concerts.
Wait-list control group


Locations

Country Name City State
United States UCSF Institute for Health & Aging San Francisco California

Sponsors (3)

Lead Sponsor Collaborator
University of California, San Francisco Department of Aging and Adults Services San Francisco, San Francisco Community Music Center

Country where clinical trial is conducted

United States, 

References & Publications (3)

Johnson JK, Gregorich SE, Acree M, Nápoles AM, Flatt JD, Pounds D, Pabst A, Stewart AL. Recruitment and baseline characteristics of the Community of Voices choir study to promote the health and well-being of diverse older adults. Contemp Clin Trials Commu — View Citation

Johnson JK, Nápoles AM, Stewart AL, Max WB, Santoyo-Olsson J, Freyre R, Allison TA, Gregorich SE. Study protocol for a cluster randomized trial of the Community of Voices choir intervention to promote the health and well-being of diverse older adults. BMC Public Health. 2015 Oct 13;15:1049. doi: 10.1186/s12889-015-2395-9. — View Citation

Johnson JK, Stewart AL, Acree M, Nápoles AM, Flatt JD, Max WB, Gregorich SE. A Community Choir Intervention to Promote Well-being among Diverse Older Adults: Results from the Community of Voices Trial. J Gerontol B Psychol Sci Soc Sci. 2018 Nov 9. doi: 10 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Physical function 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. up to 12 months
Primary Cognitive Function 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. up to 12 months
Primary Depressive Symptoms 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. up to 12 months
Secondary Health-Related Quality of Life 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 up to 12 months
Secondary Health Care Services Utilization 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 up to 12 months
Secondary Falls 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 up to 12 months
Secondary Shortness of breath We will ask three questions about shortness of breath based on Blazer and colleagues. Baseline, 6 months, 12 months up to 12 months
Secondary Balance and Endurance 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. up to 12 months
Secondary Memory and Executive Function 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. up to 12 months
Secondary Emotion 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. up to 12 months
See also
  Status Clinical Trial Phase
Completed NCT04100928 - Evaluating the Well-being Among Dental Students With Warwick-Edinburg Mental Well-Being Scale
Completed NCT01510275 - Combined Use of Respiratory Devices After Thoracic Surgery N/A
Completed NCT04576260 - Effect of CBT Intervention to Improve Sleep on Wellbeing, Dietary Intake and Food Preference N/A
Completed NCT03648164 - CREATION Health Assessment Tool for College Students
Completed NCT05430685 - The Impact of Ashwagandha on Perceived Stress, Sleep and Food Cravings in College Students Phase 2
Completed NCT02522260 - OptiTrain - Optimal Training Women With Breast Cancer N/A
Completed NCT05239429 - Improving the Mental Health and Well Being of Healthcare Providers Through the Transcendental Meditation Technique N/A
Completed NCT01501994 - Personalized Approach for Promoting Physical Activity in Mayo Clinic Physicians N/A
Recruiting NCT05447312 - Adaptive Music Therapy for Psychosocial and Cognitive Functions of Older Adults N/A