Camp NERF: Methods of a Summer Nutrition Ed Rec & Fitness Program to Prevent Unhealthy Weight Gain in Children
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ClinicalTrials.gov Identifier: NCT02908230 |
Recruitment Status :
Completed
First Posted : September 20, 2016
Last Update Posted : September 21, 2016
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The primary aims of this research project are to:
- Evaluate the efficacy of Camp NERF to improve child nutrition, physical activity, mental health, and anthropometric outcomes.
- Evaluate the efficacy of Camp NERF to improve caregiver self-efficacy for establishing healthy family nutrition and physical activity practices, amount of physical activity, and BMI.
- Evaluate the efficacy of Camp NERF to improve youth mentor nutrition, physical activity, and anthropometric outcomes.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Childhood Obesity | Behavioral: Enhanced Care Behavioral: Standard Care Behavioral: Active Control | Not Applicable |
Background: The number of obese children in the US remains high, which is problematic due to the mental, physical, and academic effects of obesity on child health. Data indicate that school-age children, particularly underserved children, experience unhealthy gains in BMI at a rate nearly twice as fast during the summer months. Few efforts have been directed at implementing evidence-based programming to prevent excess weight gain during the summer recess.
Methods: Camp NERF is an 8-week, multi-component (nutrition, physical activity, and mental health), theory-based program for underserved school-age children in grades Kindergarten - 5th grade coupled with the USDA Summer Food Service Program. Twelve eligible elementary school sites will be randomized to one of the three programming groups: 1) Active Control (non-nutrition, physical activity, or mental health [4H curricula]); 2) Standard Care (nutrition and physical activity); or 3) Enhanced Care (nutrition, physical activity, and mental health) programming. Anthropometric, behavioral, and psychosocial data will be collected from child-caregiver dyads pre- and post-intervention. Site-specific characteristics and process evaluation measures will also be collected.
Discussion: This is the first, evidence-based intervention to address the issue of weight gain during the summer months among underserved, school-aged children. Results from this study will provide researchers, practitioners, and public health professionals with insight on evidence-based programming to aid in childhood obesity prevention during this particular window of risk.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 87 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Official Title: | Camp NERF: Methods of a Theory-Based Nutrition Education Recreation and Fitness Program Aimed at Preventing Unhealthy Weight Gain in Underserved Elementary Children During Summer Months |
Study Start Date : | May 2015 |
Actual Primary Completion Date : | August 2015 |
Actual Study Completion Date : | August 2015 |
Arm | Intervention/treatment |
---|---|
Placebo Comparator: Active Control
Active Control: exposure to a non-nutrition, physical activity, or mental health curriculum/program
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Behavioral: Active Control
8-week (non-nutrition, physical activity or mental health) summer curriculum/program |
Active Comparator: Standard Care
Standard Care: exposure to a nutrition and physical activity curriculum/program
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Behavioral: Standard Care
8-week (nutrition and physical activity) summer curriculum/program |
Experimental: Enhanced Care
Enhanced Care: exposure to a nutrition, physical activity, and mental health curriculum/program
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Behavioral: Enhanced Care
8-week (nutrition, physical activity, and mental health) summer curriculum/program |
- Change in child BMI z-score [ Time Frame: Baseline and 8 weeks ]

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Ages Eligible for Study: | 4 Years to 12 Years (Child) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria (site level):
- Elementary school; USDA Summer Food Service Program open site; and 3) lacking structured programming
Exclusion Criteria:
-

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02908230
Principal Investigator: | Carolyn W Gunther, PhD | Ohio State University |
Responsible Party: | Carolyn Gunther, Assistant Professor, Ohio State University |
ClinicalTrials.gov Identifier: | NCT02908230 |
Other Study ID Numbers: |
2014B0197 |
First Posted: | September 20, 2016 Key Record Dates |
Last Update Posted: | September 21, 2016 |
Last Verified: | September 2016 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Pediatric Obesity Weight Gain Body Weight Changes Body Weight |
Obesity Overnutrition Nutrition Disorders Overweight |