Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
NCT05345041

Church-based Intervention to Improve Physical Function

Led by Rush University Medical Center · Updated on 2025-04-18

360

Participants Needed

1

Research Sites

153 weeks

Total Duration

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AI-Summary

What this Trial Is About

This is a 12-month multi-level behavioral cluster randomized trial testing a church-based intervention to improve physical function (PF) in Americans with PF limitations.

CONDITIONS

Official Title

Church-based Intervention to Improve Physical Function

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Church with membership of 300 or more adults
  • Church located in Cook, Lake, Dupage, Will, McHenry, Kane, or Kendall counties
  • Participants aged 40 or older
  • Have mobility limitations (SPPB score of 9 or less)
  • Ambulatory without assistance or use of a straight cane
  • Able to speak and read English
  • Attend the recruitment church
  • Safe to begin an exercise program as determined by the EASY Tool
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment (five or more errors on the Short-Portable Mental Status Questionnaire)
  • Unable to consistently attend group classes due to transportation, scheduling, travel, relocation, surgery, or similar issues
  • Currently participating in a medically supervised rehabilitation program (e.g., cardiac rehab)
  • Inpatient psychiatric treatment within the past 6 months or current treatment for serious psychiatric illness
  • Contraindications to exercise as determined by EASY or healthcare follow-up
  • Congestive heart failure NYHA Class I or higher, unstable angina, or recent heart attack or stroke within past 6 months
  • Visual or hearing impairment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Rush University Medical Center

Chicago, Illinois, United States, 60422

Actively Recruiting

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Research Team

E

Elizabeth M Lynch, PhD

CONTACT

Y

Yolanda Cartwright, PhD, RD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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