Childhood Obesity Clinical Trial
— SHAOfficial title:
Summer Harvest Adventure: A Garden-based Obesity Prevention Program for Children Residing in Low-resource Communities
NCT number | NCT05367674 |
Other study ID # | 2016-11075 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 1, 2017 |
Est. completion date | March 31, 2022 |
Verified date | May 2022 |
Source | Ohio State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this study is to implement and test the efficacy of the "Summer Harvest Adventure," a comprehensive garden-based behavioral, social, and environmental intervention for children (ages 8-11 years) residing in low-resource communities.
Status | Completed |
Enrollment | 200 |
Est. completion date | March 31, 2022 |
Est. primary completion date | August 31, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 8 Years to 11 Years |
Eligibility | Inclusion Criteria: - Children 8-11 years of age (as of June 1) from assenting and consenting families - English-speaking families that agree to participate; 3) residents of SNAP-eligible communities in Franklin County, Ohio. Exclusion Criteria: - Inability to functionally participate in harvesting; accommodations can be implemented in the future for children with special needs - Communication difficulties (e.g. severe developmental delay) - Lack of transportation to weekly classes or harvesting activities - Non-English speakers; because coaching and classroom-based education are all conducted in English, we will of necessity restrict to English-speakers only during this phase |
Country | Name | City | State |
---|---|---|---|
United States | The Ohio State University | Columbus | Ohio |
Lead Sponsor | Collaborator |
---|---|
Ohio State University | Nationwide Children's Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Produce intake | Change in fruit and vegetable intake as assessed by dermal skin carotenoid scores using Ramon Spectroscopy (Pharmanex NuSkin Biophotonic Scanner model S3) | Baseline and 10 weeks | |
Secondary | Weight | Change in weight will be recorded with a precision of 0.1 kilogram | Baseline and 10 weeks | |
Secondary | Family engagement | Change in family engagement as assessed by the Expressed Emotion Adjective Checklist | Baseline and 10 weeks | |
Secondary | Blood Pressure | Change in blood pressure will be measured using non-invasive brachial blood pressure assessment using oscillometric technology (automated devices) to obtain BP readings | Baseline and 10 weeks | |
Secondary | Height | Change in standing height will be measured to the nearest 1 mm using a standardized fixed stadiometer with a vertical backboard and moveable headboard | Baseline and 10 weeks | |
Secondary | BMI percentile | BMI will be calculated using weight (kg) divided by the square of height (m). BMI-for-age percentile growth charts will be used to measure the size and growth patterns of children in the study | Baseline and 10 weeks |
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