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Testing the Feasibility and Preliminary Effect of Summer Camp

Testing the Feasibility and Preliminary Effect of Summer Day Camp on Excess Summer Weight Gain in Children From Low-income Communities

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04085965
Enrollment
94
Registered
2019-09-11
Start date
2017-05-17
Completion date
2018-08-22
Last updated
2019-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Obesity Prevention

Keywords

Summer Camp, Child overweight / obesity, Diet, Physical Activity

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.

Interventions

BEHAVIORALBoys and Girls Club summer day camp

Daily camp activities included sports, games, obstacle courses, swimming and boating, summer learning and arts and crafts. Lunch was served daily via the USDA's Summer Food Service Program.

Sponsors

Hassenfeld Child Health Innovation Institute
CollaboratorUNKNOWN
The Miriam Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
RetentionBaseline to end of summer; 8 weeksNumber of participants who completed both baseline and end of summer assessments
Camp Attendance8 weeksNumber of days children attended the Boys and Girls Club Camp
Participation in Summer Activities8 weeksNumber 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

Secondary

MeasureTime frameDescription
Excess summer weight gainBaseline to end of summer; 8 weeksChange 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
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
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
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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026