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Testing the Feasibility and Preliminary Effect of Summer Camp

Not Applicable
Completed
Conditions
Childhood Obesity Prevention
Interventions
Behavioral: Boys and Girls Club summer day camp
Registration Number
NCT04085965
Lead Sponsor
The Miriam Hospital
Brief Summary

This pilot randomized controlled trial was designed to assess the feasibility and preliminary efficacy of randomizing children, ages 6-12 years from two low-income communities in Rhode Island, to attend a summer day camp (CAMP) or to experience summer as usual (SAU). Children randomized to CAMP attended a Boys and Girls Club summer day camp for 8-weeks in summer 2017 or 2018. As part of the consent process, children randomized to SAU agreed to experience an unstructured summer (i.e. not enroll in more than one week of summer camp, summer school or other structured summer programming). Primary feasibility outcomes included retention, engagement and completion of midsummer measures. Secondary outcomes, change in BMIz (a proxy for excess summer weight gain), physical activity engagement, sedentary behavior, and diet (energy intake and diet quality), were collected by blinded research staff at the end of the school year, midsummer and the end of the summer.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
94
Inclusion Criteria
  • Qualify for free or reduced-price meals at school
  • Speak English (for purposes of camp participation)
  • Agree, along with their parent(s), to randomization.
Exclusion Criteria
  • A medical condition that interferes with participation in physical activity
  • Enrollment in summer programming (camp, summer school, etc) for more than one week

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CAMPBoys and Girls Club summer day campChildren randomized to CAMP were enrolled in the Boys and Girls Club Camp in one of two low-income Rhode Island communities in summer 2017 or 2018 for 7-weeks in 2017 and 8-weeks in 2018 due to a delayed end to the 2017 school year (i.e. snow days). Camp was offered daily from 8:30 to 4:30.
Primary Outcome Measures
NameTimeMethod
Camp Attendance8 weeks

Number of days children attended the Boys and Girls Club Camp

Participation in Summer Activities8 weeks

Number of days children attended camp, summer school, or day care over the summer

Completion of study measuresBaseline (May / June); Midsummer (mid-July)

Number of participants who completed three 24-hour diet recalls and/or 7-days of actigraphy at baseline and mid-summer assessment visits

RetentionBaseline to end of summer; 8 weeks

Number of participants who completed both baseline and end of summer assessments

Secondary Outcome Measures
NameTimeMethod
Excess summer weight gainBaseline to end of summer; 8 weeks

Change in BMIz

Diet Quality4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

Change in Diet Quality as measured by the HEI-2015 from three non-consecutive 24-hour diet recalls

Sedentary Behavior4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

Change in percent time spent sedentary as measured by ActiGraph accelerometer

Physical Activity4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

Change in minutes of moderate to vigorous physical activity (MVPA) as measured by ActiGraph accelerometer

Energy Intake4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

Change in total energy intake as measured from 3 non-consecutive 24-hour diet recalls

Trial Locations

Locations (1)

The Miriam Hospital

🇺🇸

Providence, Rhode Island, United States

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