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Clinical Trials/NCT04601948
NCT04601948
Completed
N/A

AYActive Study! A Physical Health Activity Intervention

Lucas Carr1 site in 1 country14 target enrollmentNovember 6, 2019
ConditionsCancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer
Sponsor
Lucas Carr
Enrollment
14
Locations
1
Primary Endpoint
Number of steps taken per day
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this pilot study is to explore the feasibility, acceptability, and efficacy of a 6-week mobile health (mHealth) physical activity intervention among adolescent and young adult (AYA) cancer survivors being treated at the University of Iowa Hospitals and Clinics.

Detailed Description

The purpose of this pilot study is to explore the feasibility, acceptability, and efficacy of a 6-week mobile health (mHealth) physical activity intervention among adolescent and young adult (AYA) cancer survivors being treated at the University of Iowa Hospitals and Clinics. Eligible participants will receive a Fitbit activity monitor and access to the mHealth physical activity intervention for 6 weeks. The intervention will include regular motivational messages to encourage activity, a social media thread to provide social support, and a series of fun virtual walking races. AYA cancer survivors between 13-39 years are invited to participate and the impact of this intervention will be tested over 6 weeks.

Registry
clinicaltrials.gov
Start Date
November 6, 2019
End Date
September 4, 2020
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Lucas Carr
Responsible Party
Sponsor Investigator
Principal Investigator

Lucas Carr

Associate Professor

University of Iowa

Eligibility Criteria

Inclusion Criteria

  • Male and female cancer survivors
  • Diagnosed between 13 and 39 years old
  • Currently 3-24 months post-treatment (or in maintenance therapy)
  • Receiving survivorship care at HCCC/UIHC
  • In remission
  • Physically able to walk without limitations
  • Own a smartphone with a data plan that is also capable of receiving and sending texts
  • Able to understand English and provide informed assent/consent

Exclusion Criteria

  • Physically unable to walk without limitations
  • Actively receiving cancer treatment
  • Does not own a smartphone with a data plan
  • Visual or cognitive impairments causing inability to read, complete or sign the consent form and survey
  • Participants with diagnosis of thyroid cancer (due to differences in physical, psychological, emotional, and social effects)
  • Presence of a psychiatric disorder that is not managed/unstable or suicidal ideation/actuation in preceding 12 months
  • Currently meeting physical activity requirements per American Cancer Society guidelines (150 or more minutes per week of moderate to vigorous physical activity)

Outcomes

Primary Outcomes

Number of steps taken per day

Time Frame: Dail steps will be measured each day of the intervention for 7 weeks

Number of steps taken per day on each day of the intervention

Secondary Outcomes

  • PROMISE Pain Scale(Change in pain over 7 weeks)
  • PROMIS Fatigue Scale(Change in fatigue over 7 weeks)
  • PROMIS Anxiety Scale(Change in anxiety over 7 weeks)
  • Social Support for exercise(Change in social support for exercise over 7 weeks)
  • PROMIS Physical Function Scale(Change in physical function over 7 weeks)
  • PROMIS Depression Scale(Change in depression over 7 weeks)
  • Exercise Self-Regulatory Efficacy(Change in exercise self regulatory efficacy over 7 weeks)

Study Sites (1)

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