Group Intervention to Increase Physical Activity in Childhood Cancer Survivors

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-02-28

Study Completion Date

2014-02-28

Brief Summary

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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.

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Detailed Description

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Conditions

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Pediatric Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Intervention, Camp + Reunions

5 day , day camp plus 5 monthly reunions

Group Type EXPERIMENTAL

Intervention, Camp plus reunions

Intervention Type BEHAVIORAL

Control, Newsletters

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Intervention, Camp plus reunions

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

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