- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03118635
Effect of the Enhanced Summer Food Service Program on Schoolchildren (PHAST)
September 3, 2019 updated by: The Miriam Hospital
Assessing the Effect of the Enhanced Summer Food Service Program on the Health of Schoolchildren
Convergent findings from several studies document that children, especially those who are already overweight or obese or from racial / ethnic minority groups, are at risk for accelerated weight gain during the summer months.
Therefore, this project is comprised of three separate community-based interventions designed to increase access to healthy meals and physical activity opportunities to minimize excess summer weight gain in elementary school children from a diverse, low-income Rhode Island community.
Specifically, we will complete a quasi-experimental study in which we will design and deliver a physical activity intervention in conjunction with the Summer Food Service Program (SFSP) to 50 children living in a low-income, urban community.
We anticipate that the addition of physical activity programming to the SFSP, a federal program funded by the USDA which reimburses states for serving lunch meals to children during the summer in communities where at least 50% of students are eligible for free or reduced-price school meals, will increase both the acceptability and effectiveness of the SFSP and affect 1) physical activity levels, 2) sedentary behavior, and 3) diet quality.
The primary outcome (change in BMI z-score) will be compared between the 50 kids enrolled in the active intervention and 50 children enrolled in the control condition, both recruited from the same community.
Study Overview
Study Type
Interventional
Enrollment (Actual)
85
Phase
- Not Applicable
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
-
-
Rhode Island
-
Providence, Rhode Island, United States, 02906
- The Miriam Hospital
-
-
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
6 years to 12 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Low-income (defined as qualifying for free or reduced-price meals as part of the National School Lunch Program)
- Ages 6-12 years
- Ability of child to speak, read and write English (for purposes of assessment and intervention)
- Parent/guardian involvement
- Agreement to study participation
- Intent to participate in the SFSP in the upcoming summer
Exclusion Criteria:
- Medical condition that would interfere with participation in physical activity
- Enrolled in a camp or other physical activity based summer program.
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: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
No treatment control
|
|
|
Experimental: Intervention
Daily, four-hour physical activity intervention
|
Physical activity programming in accordance with the SPARK - After School curriculum as well as engaging activities provided by local community partners.
The intervention proceeded the SFSP lunch meal service, so that children received approximately three hours of physical activity programming daily.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in BMI z-score over the summer
Time Frame: Three months (summer)
|
BMI was measured at the baseline visit (early June 2016) and three months later at the end of the summer (late August, 2016).
Outcome of interest was change (BMIz at f/u - BMIz at baseline)
|
Three months (summer)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical Activity
Time Frame: Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
Activity was measured using a wrist-worn ActiGraph for 7-days.
Outcome of interest was minutes of bout-related moderate to vigorous physical activity
|
Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
|
Sedentary Behavior
Time Frame: Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
Activity was measured using a wrist-worn ActiGraph for 7-days.
Outcome of interest was percent of total wear time spent sedentary (<100 counts/minute)
|
Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
|
Energy intake
Time Frame: Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
Reported calorie intake from three, non-consecutive 24-hour diet recalls
|
Cross-sectional measure taken for 7 days during the window of weeks 4-6 of the 8 week intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 (Actual)
June 15, 2016
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
September 1, 2016
Study Registration Dates
First Submitted
April 4, 2017
First Submitted That Met QC Criteria
April 13, 2017
First Posted (Actual)
April 18, 2017
Study Record Updates
Last Update Posted (Actual)
September 4, 2019
Last Update Submitted That Met QC Criteria
September 3, 2019
Last Verified
March 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GFT640211
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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