RECRUITING

Church-based Intervention to Improve Physical Function

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Keep it Movin': A Church-based Intervention to Improve Physical Function

Quick Facts

Study Start:2023-09-21
Study Completion:2026-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05345041

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Membership of 300 or more adults
  2. * Located in Cook, Lake, Dupage, Will, McHenry, Kane, or Kendall counties
  3. * Age 40 or older
  4. * Have mobility limitations (defined as SPPB score of ≤9)
  5. * Ambulatory, defined as able to get out of a chair and walk without assistance without using a straight cane
  6. * Able to speak and read English
  7. * Attend recruitment church; and
  8. * Safe to begin an exercise program, which will be determined using the Exercise Assessment and Screening for You (EASY) Tool.
  1. * Severe cognitive impairment, defined as five or more errors on the Short-Portable Mental Status Questionnaire
  2. * Unable to consistently attend group classes at a scheduled time due to lack of reliable transportation, schedule conflicts, travel, plans to relocate, upcoming surgery, etc.
  3. * Participating in a medically supervised rehabilitation program such as cardiac rehab
  4. * Inpatient treatment for a psychiatric condition within the past 6 months, or currently receiving treatment for schizophrenia or other serious psychiatric illness
  5. * Contraindications to exercise determined using the EASY/healthcare follow-up
  6. * Congestive heart failure New York Health Association (NYHA) Class I or higher; unstable angina; heart attack or stroke within past 6 months
  7. * Visual or hearing impairment.

Contacts and Locations

Study Contact

Elizabeth M Lynch, PhD
CONTACT
3125632254
elizabeth_lynch@rush.edu
Yolanda Cartwright, PhD, RD
CONTACT
3129429697
yolanda_cartwright@rush.edu

Study Locations (Sites)

Rush University Medical Center
Chicago, Illinois, 60422
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-21
Study Completion Date2026-09-01

Study Record Updates

Study Start Date2023-09-21
Study Completion Date2026-09-01

Terms related to this study

Additional Relevant MeSH Terms

  • Physical Function
  • Multiple Chronic Conditions