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CompletedNCT04085965Updated Sep 11, 2019

Testing the Feasibility and Preliminary Effect of Summer Camp

An interventional study of Boys and Girls Club summer day camp in Childhood Obesity Prevention, sponsored by The Miriam Hospital. Completed at 1 site in United States. Open to participants aged 6 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-11.

Sponsored by The Miriam Hospital · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 2 years 3 months after the study started (first participant enrolled May 2017, registered Sep 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Randomized
Ages
6 Years to 12 Years
Sex
All
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Study 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.

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Conditions studied

  • Childhood Obesity Prevention

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Keywords

  • Summer Camp
  • Child overweight / obesity
  • Diet
  • Physical Activity
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In context

Pediatric Obesity

1,117 studies on the registry are indexed under Pediatric Obesity; 189 are open to participants now.

This study's enrollment of 94 is close to the median of 103 across 862 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

The Miriam Hospital is the lead sponsor of 178 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
6 Years to 12 Years
Sexes eligible
All
Accepts 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

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
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    CAMP

    Children 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.

    Behavioral: Boys and Girls Club summer day camp

  • No intervention
    Summer As Usual

    Children randomized to the SAU group were asked to experience an unstructured summer as otherwise planned by their parent / guardian. They agreed to not attend structured summer programming (i.e. camp, summer school, or day care) for more than one week over the summer so as to provide an inactive control group for comparison to those in CAMP.

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.

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What researchers measure

Primary outcomes

  1. Retention

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

    Time frame: Baseline to end of summer; 8 weeks

  2. Camp Attendance

    Number of days children attended the Boys and Girls Club Camp

    Time frame: 8 weeks

  3. Participation in Summer Activities

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

    Time frame: 8 weeks

  4. Completion of study measures

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

    Time frame: Baseline (May / June); Midsummer (mid-July)

Secondary outcomes

  1. Excess summer weight gain

    Change in BMIz

    Time frame: Baseline to end of summer; 8 weeks

  2. Physical Activity

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

    Time frame: 4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

  3. Sedentary Behavior

    Change in percent time spent sedentary as measured by ActiGraph accelerometer

    Time frame: 4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

  4. Energy Intake

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

    Time frame: 4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

  5. Diet Quality

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

    Time frame: 4-6 weeks (from baseline (end of May / beginning of June) to mid-summer (mid-July))

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Study locations

1 site
  • The Miriam Hospital
    Providence, Rhode Island 02906, United States
08

References and documents

Publications

  • Evans EW, Wing RR, Pierre DF, Howie WC, Brinker M, Jelalian E. Testing the effect of summer camp on excess summer weight gain in youth from low-income households: a randomized controlled trial. BMC Public Health. 2020 Nov 17;20(1):1732. doi: 10.1186/s12889-020-09806-y. PubMed 33203385 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 11, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04085965
Lead sponsor
The Miriam Hospital
Collaborators
Hassenfeld Child Health Innovation Institute
Responsible party
Sponsor
First posted
Sep 11, 2019
Start date
May 17, 2017
Primary completion
Aug 22, 2018
Completion
Aug 22, 2018
Last update
Sep 11, 2019

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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