Home Plate: A Trial to Improve Home Food Preparation Practices Among Parents of Toddlers
NCT ID: NCT02458833
Last Updated: 2019-04-24
Study Results
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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COMPLETED
NA
115 participants
INTERVENTIONAL
2015-06-30
2017-07-13
Brief Summary
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Detailed Description
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1. Test the intervention's effect on diet and physical health.
Hypothesis 1: The intervention group will have improved home food preparation practices and a healthier diet compared to the control group.
2. Test the intervention's effect on family health.
Hypothesis 2: The intervention group will report improved parenting skills and more hopeful patterns of thinking.
3. Identify factors present at baseline and during engagement with the intervention that distinguish intervention participants who have improved diet, physical health, and family health from those who do not.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Intervention
Behavioral: Home Plate intervention
Home Plate
Home Plate is a community-based, peer mentored intervention aimed at improving home food preparation practices in families with young children. Through 6 classes, this intervention explores topics related to regularly preparing healthy foods at home.
Delayed Entry Control
This Arm will receive the Home Plate intervention 3 months after the Intervention Arm completes the intervention.
Home Plate
Home Plate is a community-based, peer mentored intervention aimed at improving home food preparation practices in families with young children. Through 6 classes, this intervention explores topics related to regularly preparing healthy foods at home.
Interventions
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Home Plate
Home Plate is a community-based, peer mentored intervention aimed at improving home food preparation practices in families with young children. Through 6 classes, this intervention explores topics related to regularly preparing healthy foods at home.
Eligibility Criteria
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Inclusion Criteria
2. Able to give informed consent.
3. Legal guardian and caregiver of at least one child, age 1-3 years
1. 1-3 year old children of mentee primary caregivers enrolled in the study
2. If a mentee caregiver has more than one child, then all their eligible children (ages 1-3 years) will be enrolled in the study.
In addition,
2. The study team will decide which participants will be invited to be peer mentors, based on attributes including interest, leadership ability, and home food preparation skills.
2. Caregivers who are pregnant at the time of enrollment.
3. Caregivers or children with a medical condition that significantly affects their diet or eating habits. (The study team will ask during the time of recruitment if subjects or their children have a medical condition that significantly affects diet or eating habits.)
4. Subjects who, in the opinion of the Investigator, may be unable to participate in the study schedules or procedures.
18 Years
ALL
No
Sponsors
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University of Pennsylvania
OTHER
Children's Hospital of Philadelphia
OTHER
Responsible Party
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Principal Investigators
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Senbagam Virudachalam, MD, MSHP
Role: PRINCIPAL_INVESTIGATOR
Children's Hospital of Philadelphia
Locations
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The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Countries
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Other Identifiers
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15-011720
Identifier Type: -
Identifier Source: org_study_id
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