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Clinical Trials/NCT05417438
NCT05417438
Completed
Not Applicable

Survivor mHealth: Assessing Feasibility of a Wearable Device and App in Cancer Survivors

University of Massachusetts, Worcester1 site in 1 country31 target enrollmentStarted: January 15, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
University of Massachusetts, Worcester
Enrollment
31
Locations
1
Primary Endpoint
Feasibility of Enrollment

Overview

Brief Summary

The Survivor mobile health (mHealth) study is testing the use of wearable devices (Fitbits) and a smartphone application in cancer survivors. The goal of the program is to increase survivor's physical activity levels. The Fitbit will be synced to the app and participants will receive messages and notifications about their activity levels. Participants will also complete surveys through the app asking how useful it is and ways to improve it. The study team will conduct qualitative interviews at the completion of the 3 months to see how participants liked the program, and ways it can be improved and make it more specific to cancer survivors. The study team will also conduct interviews with providers and clinic staff to assess their perceptions of patient digital health programs and preferences for receiving patient-generated health data.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Past cancer diagnosis
  • At least 18 years of age
  • Capacity to provide informed consent
  • Medically cleared to perform physical activity (as noted by Physical Activity Readiness Questionnaire form or physician's clearance if needed)
  • Owns a smartphone
  • Aims 1 and 2

Exclusion Criteria

  • Is a prisoner
  • Non-English speaking
  • Is unable to provide consent
  • Under 18 years of age
  • No prior cancer diagnosis
  • Does not own a smartphone
  • Aim 3 Inclusion Criteria:
  • Are a current UMass Memorial Cancer Clinic patient navigator, oncologist, radiologist, or cardiologist
  • Consent to participate
  • Aim 3 Exclusion Criteria:

Outcomes

Primary Outcomes

Feasibility of Enrollment

Time Frame: Baseline

Feasibility will be determined by a participant meeting all three criteria: 1) Enrollment in trial, 2) completion of baseline measures, and 3) Fitbit sync to app.

Secondary Outcomes

  • 3-month Daily Step Count(At study completion, within 3-months of enrollment)
  • 1-Month Usability Overall APP Rating(1-month post-enrollment)

Investigators

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

Jamie Faro

Assistant Professor

University of Massachusetts, Worcester

Study Sites (1)

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