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Clinical Trials/NCT01835509
NCT01835509
Completed
Early Phase 1

Group Intervention to Increase Physical Activity in Childhood Cancer Survivors

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins1 site in 1 country20 target enrollmentFebruary 2013

Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Pediatric Cancer
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Enrollment
20
Locations
1
Primary Endpoint
Change in level of physical activity
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The primary aim of this randomized, controlled study is to evaluate the impact and feasibility of a prolonged physical activity intervention in school-aged childhood cancer survivors who self-report sedentary lifestyles. The study will test the hypothesis that childhood cancer survivors participating in a physical activity intervention guided by Social Cognitive Theory will increase the amount of time spent daily in moderate to vigorous physical activity, and improve exercise self-efficacy compared to children randomized to usual care. A secondary aim is to assess the impact of the intervention on cardiovascular risk factors including fitness and body composition.

Registry
clinicaltrials.gov
Start Date
February 2013
End Date
February 2014
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Cancer survivors ages 8-12 years.
  • Off therapy for at least 3 months and not more than 5 years and in remission.
  • Medical clearance to participate in physical activities from the survivor's primary oncology provider;
  • Self-report of \< 60 minutes of moderate to vigorous physical activity (MVPA) per day.
  • Must be able to ambulate.
  • Signed informed consent/assent.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in level of physical activity

Time Frame: change from pre-study and at 6months after camp

Physical activity will be measured with Accelerometers worn for 4 days pre-study and six months later

Secondary Outcomes

  • Change in Self efficacy(Change in self efficacy measrued prestudy and 6 months after camp)

Study Sites (1)

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