Aging Mastery Program® (AMP) Evaluation

Healthy Clinical Trial

— AMP  

Official title:

Evaluation of Aging Mastery Program® in Senior Centers Throughout Los Angeles County

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03342729
• Other study ID #: IRB #17-000137
• Status: Completed
• Phase: N/A
• Start date: May 1, 2017
• Est. completion date: March 15, 2018

Study information

• Verified date: December 2019
• Source: University of California, Los Angeles
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The Aging Mastery Program® (AMP) is designed to inform, encourage, and support older adults as they take steps to improve their lives and stay engaged in their communities. The program incorporates evidence-informed materials, expert speakers, group discussion, peer support, and small rewards to give participants the skills and tools they need to achieve measurable improvements in managing their health, remaining economically secure, and contributing actively to society. L.A. CAPRA in partnership with the National Council on Aging, City of Los Angeles and the Los Angeles County Department of Aging will evaluate the effectiveness of the AMP program across 5 community-based senior sites. The overall objective of the proposed study is to evaluate the effectiveness of AMP program on improving the health and well-being of older adults using a randomized wait-list controlled trial.

Description:

The Aging Mastery Program® (AMP) offers community-based organizations a clear path to engage older adults and address the physical, financial, and emotional wellness of older adults. First piloted nationally in five senior centers, AMP incorporates evidence-based materials, expert speakers, group discussion, and peer support to give participants the skills and tools they need to achieve measurable improvements in managing their health and remaining economically secure. The program aims to empower seniors to make and maintain small, impactful changes to their behaviors to live a healthier, happier, and more secure life. AMP has been field-tested in various rural and urban setting, senior centers, and across an ethnically diverse middle-aged and older adult population, reaching almost 6,000 since 2013. Currently, the program is being evaluated through a quasi-experimental study in New York State and under consideration as an evidence-based program.

The National Council on Aging study team will train six program leads from the City of Los Angeles Department of Aging and Los Angeles Area on Aging to implement Aging Mastery Program® (AMP). The intervention will consist of a 10-week series held once-a-week for an hour and half (90 minutes). It will be group-based and led by trained facilitators and designated expert speakers in a community-based setting (senior centers). The program reviews 10 central areas of aging (1) navigating longer lives, (2) physical activity, (3) sleep, (4) healthy eating and hydration, (5) financial security, (6) medication management, (7) advance care planning, (8) healthy relationships, (9) falls prevention, and (10) community engagement. The intervention is based in social cognitive theory and attribution retraining and incorporates elements such as verbal persuasion, goal setting, problem solving, and attribution retraining techniques that encourage students to adopt controllable and unstable explanations.

Study Participants (N=200 or n=40/site) will be recruited from 5 study sites to participate in the Aging Mastery Program. UCLA study personnel will be on-site to consent older adults to participate in the evaluation of intervention and take part of baseline and post-intervention assessments. Upon signing the consent, study staff will collect self-administered baseline data (measures and measurement tools --i.e. Patient Information Survey, PROMIS and Patient Activation Survey (PAM) from all participants (n=200). After baseline data has been collected, participants will be randomized and assigned to either the immediate intervention groups (n=100 intervention) or the wait-list control (n=100). At each site, forty participants will be in the intervention group and 40 will be in wait-list control. Following the 10-week Aging Mastery Program®, post-intervention assessment (measures and measurement tools --i.e. Patient Information Survey, Patient Satisfaction, PROMIS and PAM) will be administered. During the data collection sessions, study staff will go to community sites and collect post-treatment self-reported assessment

Recruitment information / eligibility

• Status: Completed
• Enrollment: 180
• Est. completion date: March 15, 2018
• Est. primary completion date: March 15, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 50 Years to 100 Years

Eligibility

Inclusion Criteria:

1. Available to attend the baseline and post-treatment data collection session and subsequent weekly intervention sessions

2. Available to speak and understand English

3. Plans to be living in the region during the next 6 months

4. Has cognitive ability to provide informed consent to participate

Exclusion Criteria:

1. Cannot Speak or Communicate well in English

2. Unavailable to attend the baseline data collection session and subsequent weekly intervention sessions

3. Plans to move away from the region during the next 6 months

4. Lacks cognitive ability to provide informed consent to participate

Related Conditions & MeSH terms

• Aging
• Healthy
• Older Adults

Intervention

Behavioral:
• Intervention
Participants receive the AMP 10-week program immediately
• Control
Participants will not received the AMP 10-week program immediately, rather will wait 3-months

Locations

Country	Name	City	State
United States	Antelope Valley Senior Center	Lancaster	California
United States	Freda Mohr Multipurpose Center	Los Angeles	California
United States	Potrero Heights Community Center	Montebello	California
United States	San Pedro Service Center	San Pedro	California
United States	Sherman Oaks East Valley Adult Center	Sherman Oaks	California

Sponsors (4)

Lead Sponsor	Collaborator
University of California, Los Angeles	City of Los Angeles Department of Aging, Los Angeles County Area Agency on Aging, The National Council on Aging

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Improvements in health and well-being	Patient self-reported questionnaire PROMIS scale; SF-16	Pre-intervention (baseline) and questions will be repeated again 10-weeks after the baseline (for waitlist control/for those in class immediately after the class) as a Post-intervention.
Primary	Improvements in Patient Activation	Patient self-reported questionnaire PAM scale	Pre-intervention (baseline) and questions will be repeated again 10-weeks after the baseline (for waitlist control/for those in class immediately after the class) as a Post-intervention.