COMPLETED

Physical Activity and Percussive Massage Therapy for Reducing Pain in Older Women

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

Over 60% of women aged 65 and older suffer from pain, yet this group is underrepresented in research. Physical activity and percussive massage therapy may help manage pain, but both require consistent engagement, making long-term participation challenging for most people. Self-monitoring could improve adherence to these pain management efforts, but the optimal strategies for self-monitoring remain unknown. This is a a 2x2 factorial randomized controlled trial in older women (N = 108) to determine which behavior(s) should be self-monitored to (1) promote engagement in physical activity and percussive massage therapy and (2) reduce pain. This study design will allow examination on effects of self-monitoring across different behaviors to identify the most effective strategies for improving pain management adherence and reducing pain.

Official Title

Physical Activity and Percussive Massage Therapy for Reducing Pain in Older Women

Quick Facts

Study Start:2025-01-15
Study Completion:2025-11-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT07056335

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:65 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Older aged female (65 years of age or older)
  2. 2. Self-report pain as a barrier to PA
  3. 3. Self-report not engaging in regular aerobic physical activity
  4. 4. Express an interest in increasing PA levels.
  5. 5. Proficient in English
  6. 6. Own an IOS or Android smartphone with regular internet access
  7. 7. Check emails at least daily
  8. 8. Capable of providing informed consent
  9. 9. Willing to use a massage gun for 3 months
  10. 10. Live in continental US
  1. 1. Planned surgery that limits mobility in the next 2 months.
  2. 2. Concurrently participating in other pain management or physical activity programs
  3. 3. Cancer-related pain
  4. 4. Neurological disorder that affects cognition
  5. 5. Mobility impairments that prevent unassisted walking.
  6. 6. Receiving active medical treatment that would impair protocol compliance

Contacts and Locations

Principal Investigator

Shiyu Li, PhD
PRINCIPAL_INVESTIGATOR
University of Michigan

Study Locations (Sites)

University of Michigan
Ann Arbor, Michigan, 48109
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • Shiyu Li, PhD, PRINCIPAL_INVESTIGATOR, University of Michigan

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 Date2025-01-15
Study Completion Date2025-11-01

Study Record Updates

Study Start Date2025-01-15
Study Completion Date2025-11-01

Terms related to this study

Keywords Provided by Researchers

  • behavior change

Additional Relevant MeSH Terms

  • Pain, Chronic