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Clinical Trials/NCT06267547
NCT06267547
Active, Not Recruiting
N/A

Healthy Activities Improve Lives Randomized Control Trial

Massachusetts General Hospital1 site in 1 country120 target enrollmentApril 23, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Physical Activity
Sponsor
Massachusetts General Hospital
Enrollment
120
Locations
1
Primary Endpoint
Acceptability (Feedback Form)
Status
Active, Not Recruiting
Last Updated
6 months ago

Overview

Brief Summary

The investigators have developed an online platform to support the 8-week, F&S! exercise program called the Healthy Activity Improves Lives (HAIL) online platform. The aim of this study is to perform a cluster randomization of four racially diverse churches or senior centers to either the standard F&S! program, or the combined HAIL Online Platform + F&S! program to examine the efficacy of the HAIL online platform + F&S! program for older adults in black communities.

Detailed Description

This is randomized clinical trial of cluster randomization evaluating the efficacy and feasibility of the HAIL online platform + F\&S! program. We will enroll four cohorts (i.e., at two racially diverse churches or senior centers) for a total number of 120 participants. We will use a phone screen to assess participants' eligibility and explain the study procedures. Eligible individuals will then be given a link to complete an e-Consent in REDCap. Those randomized into the intervention group will also receive instructions on how to access the HAIL online platform to complete assessments as part of the baseline visit. Participants in both the intervention and comparison groups will complete the 8-week F\&S! exercise program which will be delivered in-person as well as remote. Participants in the intervention group will have access to the adjunct HAIL online platform during the F\&S! program, and then continue to use the HAIL online platform during the 3-mo follow-up.

Registry
clinicaltrials.gov
Start Date
April 23, 2024
End Date
February 1, 2027
Last Updated
6 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Louisa Grandin Sylvia

Associate Director and Associate Professor

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Individuals over the age of 55 years
  • Participants are able to travel to one of the churches for the in-person F\&S! exercise sessions
  • Participants cannot be currently participating in a regular PA program (i.e., at least 100 min per week of moderate to vigorous physical activities)

Exclusion Criteria

  • Participants do not understand study procedures or are unable to participate in the verbal consent process
  • Participants must have a physician responsible for their medical care
  • Participants endorse an item on the Revised Physical Activity Readiness Questionnaire (rPAR-Q) as confirmed by their treating physician
  • Participants who report any contraindication to exercising (e.g., recent ECG changes or myocardial infarction, unstable angina, uncontrolled arrhythmias, third degree heart block, congestive heart failure)
  • Participants who receive a score of 28 or higher on the Telephone Interview for Cognitive Status (TICS) during pre-screening

Outcomes

Primary Outcomes

Acceptability (Feedback Form)

Time Frame: Week 20

Acceptability will be assessed by the HAIL online Feedback form. We will develop a form to ask for tailored feedback on the F\&S! program and the HAIL online platform to better understand participants' satisfaction with specific aspects of this online program.

Feasibility and Retention

Time Frame: Week 20

Retention will be assessed by how many individuals completed the 3-month post-intervention follow-up

Acceptability (Exit Interviews)

Time Frame: Week 20

Acceptability will finally be assessed with focus group exit interviews, which will be qualitatively coded.

Acceptability

Time Frame: Week 8

Acceptability will be assessed by the Client Satisfaction Questionnaire (CSQ-8). The CSQ-8 assesses acceptability and feasibility of the HAIL online platform and has demonstrated good reliability and validity. Total scores range from 8 to 32, with the higher number indicating greater satisfaction.

Secondary Outcomes

  • Changes in Anxiety(Weeks 0, 8, 20)
  • Changes in Physical Activity (MVPA)(Weeks 0, 8, 20)
  • Changes in Physical Strength(Weeks 0, 8, 20)
  • Chronic Conditions(Week 0)
  • Changes in Physical Functioning(Weeks 0, 8, 20)
  • Utilization of Healthcare Resources(Week 0)
  • Changes in Physical Activity (Steps)(Weeks 0, 8, 20)
  • Changes in Aerobic Capacity(Weeks 0, 8, 20)
  • Motivation to Change(Week 0)
  • Fall History(Week 0)
  • Changes in Depression(Weeks 0, 8, 20)
  • Changes in Confidence in Exercises(Weeks 0, 8, 20)
  • Changes in Overall Wellbeing(Weeks 0, 8, 20)
  • Changes in Social Isolation(Weeks 0, 8, 20)

Study Sites (1)

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