Physical Activity Intervention for Sedentary Childhood Cancer Survivors
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.
Intervention, Camp plus reunions
Neoplasms
Supportive Care Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
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.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
No InterventionStudy 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