- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01835509
Group Intervention to Increase Physical Activity in Childhood Cancer Survivors
February 24, 2014 updated by: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Early Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Maryland
-
Baltimore, Maryland, United States, 21287
- Sidney Kimmel Comprehensive Cancer Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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:
None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention, Camp + Reunions
5 day , day camp plus 5 monthly reunions
|
|
No Intervention: Control, Newsletters
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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
|
change from pre-study and at 6months after camp
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Self efficacy
Time Frame: Change in self efficacy measrued prestudy and 6 months after camp
|
Self efficacy is measured with a questionnaire
|
Change in self efficacy measrued prestudy and 6 months after camp
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2013
Primary Completion (Actual)
February 1, 2014
Study Completion (Actual)
February 1, 2014
Study Registration Dates
First Submitted
April 11, 2013
First Submitted That Met QC Criteria
April 18, 2013
First Posted (Estimate)
April 19, 2013
Study Record Updates
Last Update Posted (Estimate)
February 25, 2014
Last Update Submitted That Met QC Criteria
February 24, 2014
Last Verified
February 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- J12136
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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