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Clinical Trials/NCT05870176
NCT05870176
Enrolling By Invitation
Not Applicable

ActivityChoice: A Clinic-delivered Implementation Program to Increase Physical Activity and Decrease Cardiovascular Disease Risk Amongst Cancer Survivors

University of Massachusetts, Worcester1 site in 1 country114 target enrollmentSeptember 11, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Massachusetts, Worcester
Enrollment
114
Locations
1
Primary Endpoint
Proportion of patients referred as obtained by the electronic referral system and electronic health record
Status
Enrolling By Invitation
Last Updated
5 months ago

Overview

Brief Summary

Cardiovascular disease, the number one leading cause of death in the United States, is highly prevalent in cancer survivors. Physical activity can reduce risk, and referrals to programs addressing survivors' choices are highly recommended from providers in cancer survivorship, though rarely implemented. The study team proposes to develop ActivityChoice, a clinic-based implementation program, using patient narrative decision aids to support choices to a group in-person, group virtual, or self-monitored digital health physical activity program.

Registry
clinicaltrials.gov
Start Date
September 11, 2023
End Date
November 1, 2026
Last Updated
5 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Principal Investigator
Principal Investigator

Jamie Faro

Assistant Professor

University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Proportion of patients referred as obtained by the electronic referral system and electronic health record

Time Frame: Baseline

The number of patients referred/The number of eligible patients

Secondary Outcomes

  • Proportion of eligible clinicians enrolling in the the study(Baseline)
  • Patient Engagement(Examined at baseline, 3-, and 6-months)
  • Clinic/Clinician fidelity of delivering patient decision aids(Baseline)
  • Patient Retention(3- and 6-months)
  • Patient Autonomous Regulation(Baseline, 3- and 6-months)
  • Patient Self-Report Physical Activity(Baseline, 3- and 6-months)
  • Patient narrative decision aid acceptability and effectiveness (Enhanced Referral only)(Baseline following referrals)
  • Patient Health-related Quality of Life(Baseline, 3- and 6-months)
  • Patient Objective Physical Activity(Baseline, 3- and 6-months)

Study Sites (1)

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