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Clinical Trials/NCT05216380
NCT05216380
Completed
Not Applicable

ActivityLink: Clinic-to-Community Physical Activity Referrals for Cardiovascular Disease Risk Reduction in Cancer Survivors.

University of Massachusetts, Worcester1 site in 1 country69 target enrollmentMarch 15, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Massachusetts, Worcester
Enrollment
69
Locations
1
Primary Endpoint
The Number of Patients Referred Using the Secure Webform
Status
Completed
Last Updated
last year

Overview

Brief Summary

Background: Cancer survivors have a greater risk of cardiovascular disease (CVD) and have low physical activity levels. Physical inactivity is one modifiable risk factor for CVD, and increased physical activity has shown a cardioprotective effect on lowering CVD risk. The objective of ActivityLink is to use an electronic referral (e-referral) implementation program for clinic staff to refer survivors to an in-person and a virtual physical activity program.

Methods: Participants in this study will include clinic staff and patients. Investigators will first conduct interviews with clinic staff and patients, followed by usability testing of a referral system with staff. The study team will then beta-test two rounds of testing using Plan, Do, Study, Act (PDSA) Cycles for clinic staff to refer patients in the clinic. Quantitative data and qualitative interviews will be collected following each PDSA cycle, with refinements made based on feedback.

Outcomes: The proposed study addresses a critical need to implement physical activity referrals into routine cancer survivorship visits.

Registry
clinicaltrials.gov
Start Date
March 15, 2021
End Date
June 12, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
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

The Number of Patients Referred Using the Secure Webform

Time Frame: 12 weeks from launch of referrals (baseline)

The number of patients clinicians referred using the secure webform

Secondary Outcomes

  • Proportion of Eligible Clinic Staff Who Enroll(12 weeks from launch of referrals (baseline))
  • Proportion of Referred Patients Who Enroll in Programs(At study completion, within 3 months of referral completion)

Study Sites (1)

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