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Clinical Trials/NCT04203030
NCT04203030
Completed
N/A

Physical Activity to Improve Physical Function in a Community-Based Health Ministry in Chicago's West Side

Rush University Medical Center1 site in 1 country15 target enrollmentDecember 16, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aging
Sponsor
Rush University Medical Center
Enrollment
15
Locations
1
Primary Endpoint
Physical Function
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study is being conducted to test if a program with physical activity and learning about movement (including goal setting, benefits of physical activity, and how to increase physical activity gradually) helps people to become more active and to move better. The physical activity program involves specific exercises done in a group setting, and the education part will involve learning about different ways to move to make everyday activities easier. The program will last 16 weeks. This program will take place in a large fellowship area of a partner church through an established community-based participatory research partnership in Chicago, IL.

Detailed Description

Limitations in physical function (PF) are related to decreased quality of life and are predictive of disability, nursing home admission, increased healthcare costs, and mortality in older adults. Structured physical activity has been shown to prevent mobility disability among those with physical function limitations, though community-based programs are needed, particularly in underserved communities. The purpose of this study is to pilot test a tailored physical activity intervention in churches in Chicago's West Side through an existing community-based participatory research partnership. The investigators previously found high rates of physical function limitations in these communities, and through qualitative research have identified intervention components that may aid in promoting physical activity among community members with physical function limitations. The primary aim is test the intervention in a 16 week, proof-of-concept study in 20 participants who are ambulatory but have PF limitations. The group-based physical activity intervention will take place in a large common area of a church. For feasibility the investigators will be testing the intervention in one church. The intervention will be delivered over 16 weeks, with assessments at baseline and 16 weeks.

Registry
clinicaltrials.gov
Start Date
December 16, 2019
End Date
September 4, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brittney Lange-Maia

Assistant Professor in Preventive Medicine

Rush University Medical Center

Eligibility Criteria

Inclusion Criteria

  • Age 40 or older
  • Not currently participating in another formal exercise program and perform less than 150 minutes per week of exercise
  • Ambulatory, defined as able to get out of a chair and walk without assistance aside from using a straight cane.
  • Have any difficulty: Walking ¼ mile, (about 2-3 blocks) OR Walking up 10 steps without resting
  • Speak English
  • Safe to begin an exercise program (determined using the Exercise Assessment and Screening for You (EASY) Tool. Physician clearance may be needed based upon EASY Screening recommendations

Exclusion Criteria

  • Severe cognitive impairment, defined as five or more errors on the Short-Portable Mental Status Questionnaire
  • Plans to move out of the geographic area during the study period
  • Plans to have major surgery within the study period Anticipate having major schedule changes that would interfere with ability to participate in the program.
  • Inability to get to intervention location on a weekly basis
  • Unwilling to commit to a weekly, approximately 90 minute program for 16 weeks.
  • Contraindications to exercise determined using the EASY/healthcare follow-up.
  • Self-reported
  • Heart disease
  • Uncontrolled diabetes mellitus
  • Pacemaker

Outcomes

Primary Outcomes

Physical Function

Time Frame: 16 weeks

Change in Short Physical Performance Battery score Scale ranges from 0-12 (integers only) with higher scores indicating better function.

Secondary Outcomes

  • Physical Activity (Objective)(16 weeks)
  • Physical Activity (Self-Reported)(16 weeks)
  • Acceptability of intervention:(16 weeks)

Study Sites (1)

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