An Adaptive Design for Dosing Physical Activity Among Older Cancer Survivors Who Experience Chronic Pain: a Micro-randomized Trial
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this study is to assess the best time to deliver a message to increase physical activity and how often participants will experience a pain episode in the 24 hours following their receipt of a message to increase physical activity.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Healthy Volunteers: f
View:
• Age greater than or equal to 65 years.
• Patients with a history of bladder, breast, cervical, colorectal, endometrial, lung, and prostate cancer diagnosis and treatment.
• Fluent in spoken and written English.
• Patient has access to smartphone
• Ability to understand a written informed consent document, and the willingness to sign it.
Locations
United States
Wisconsin
Froedtert Hospital
RECRUITING
Milwaukee
Contact Information
Primary
Kelly Clohesey Clinical Research Coordinator, MOT
kclohesey@mcw.edu
4149554099
Backup
Whitney Morelli, PhD
wmorelli@mcw.edu
Time Frame
Start Date: 2025-12
Estimated Completion Date: 2026-12
Participants
Target number of participants: 50
Treatments
Experimental: Micro-randomized trial study arm
In this one-armed, 4-week trial, participants will receive prompts to report their pain symptoms 4 times throughout the day. Participants may receive up to 4 reminders to move messages throughout the day to promote participants to engage in physical activity. The receipt of messages is randomized each day. Participants will wear a research-grade activity monitor throughout the duration of their participation in the intervention to measure physical activity behaviors.
Related Therapeutic Areas
Sponsors
Leads: Medical College of Wisconsin
Collaborators: National Cancer Institute (NCI)