Testing the Feasibility and Preliminary Effect of Summer Camp

NCT ID: NCT04085965

Last Updated: 2019-09-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-05-17

Study Completion Date

2018-08-22

Brief Summary

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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

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Conditions

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Childhood Obesity Prevention

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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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.

Group Type EXPERIMENTAL

Boys and Girls Club summer day camp

Intervention Type BEHAVIORAL

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.

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.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Boys 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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hassenfeld Child Health Innovation Institute

UNKNOWN

Sponsor Role collaborator

The Miriam Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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The Miriam Hospital

Providence, Rhode Island, United States

Site Status

Countries

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United States

References

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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.

Reference Type DERIVED
PMID: 33203385 (View on PubMed)

Other Identifiers

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710-9073

Identifier Type: -

Identifier Source: org_study_id

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