Completed

Physical Activity Intervention for Sedentary Childhood Cancer Survivors

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Study Aim

This study aims to evaluate the change in physical activity levels in sedentary childhood cancer survivors, measured using accelerometers worn for 4 days before the study and six months later.

What is being tested

Intervention, Camp plus reunions

Behavioral
Who is being recruted

Neoplasms

From 8 to 12 Years
See all eligibility criteria
How is the trial designed

Supportive Care Study

Early Phase 1
Interventional
Study Start: February 2013
See protocol details

Summary

Principal SponsorSidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Last updated: February 25, 2014
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2013

Actual date on which the first participant was enrolled.

This study focuses on childhood cancer survivors who lead inactive lifestyles. Its main goal is to test if a long-term physical activity program, based on Social Cognitive Theory, can help these children become more active and confident about exercising. The study is important because it aims to improve the quality of life for childhood cancer survivors, addressing the common challenge of inactivity among this group. During the study, participants wear accelerometers for 4 days before the study and again six months later. These devices measure the level of physical activity. The hope is that children who participate in the program will show an increase in daily moderate to vigorous physical activity. The study also looks at how the program might affect cardiovascular risk factors, such as fitness and body composition.

Principal SponsorSidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Last updated: February 25, 2014
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

20 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 8 to 12 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neoplasms

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: None

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
5 day , day camp plus 5 monthly reunions

Group II

No Intervention

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Sidney Kimmel Comprehensive Cancer Center

Baltimore, United StatesOpen Sidney Kimmel Comprehensive Cancer Center in Google Maps
CompletedOne Study Center