- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03071419
A Nutrition and Parenting Program for Fathers and Their Pre-school Age Children
June 4, 2019 updated by: Amy Mobley, University of Connecticut
Father-Focused Nutrition and Parenting Program to Help Prevent Childhood Obesity in Preschool Age Children
This pilot study evaluates the feasibility and impact of a father-focused childhood obesity prevention program on paternal food-related parenting practices, mealtime behaviors and father/child nutrition and physical activity behaviors.
Half of participants (low-income father and child dyads) will receive an intervention immediately while the other half of participants will serve as a wait-list control group and receive the intervention at a later date.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
All participants (low-income father and child dyads) will receive an 8 session (2 hours/session) (DAD) including community-based, hands-on, nutrition and parent education intervention with between-session technology enhancements.
Dyads will be randomly assigned within groups of 10 to DAD or a wait-list control group (DELAY).
Assessments will be conducted at pre, post and 1 month post including a subset of data from cohabiting mothers to assess moderating influences on outcomes.
Study Type
Interventional
Enrollment (Actual)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
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East Hartford, Connecticut, United States, 06118
- Hockanum School, Head Start Program
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Manchester, Connecticut, United States, 06042
- Manchester Preschool Center
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- "Father" eligible for a federal food assistance or related program (e.g. SNAP) or living in an area with >30% poverty
- Having at least one preschool age child (ages 3-5 years old)
- At least 18 years of age and able to speak English
Exclusion Criteria:
- No presence or interaction with child during meal or snack times.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Nutrition and Parenting Intervention
Participants (n=30, father/child dyads in groups of 10) will receive an 8 session (2 hours/session) community-based intervention including nutrition and parent education with between-session technology enhancements.
|
The proposed intervention will evaluate and explore the unique influences that low-income fathers have on their preschool age children's obesogenic behaviors and obesity risk.
|
Active Comparator: Wait-list Control
Participants (n=30, father/child dyads in groups of 10) will serve as a wait-list control group and receive the same Nutrition and Parenting Intervention after completing pre and post assessments several weeks apart.
|
The proposed intervention will evaluate and explore the unique influences that low-income fathers have on their preschool age children's obesogenic behaviors and obesity risk.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Comprehensive Feeding Practices Questionnaire
Time Frame: Change from baseline at 8 weeks
|
Food-related parenting practices including parental support, control, structure, feeding
|
Change from baseline at 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Father & child diet quality
Time Frame: Change from baseline at 8 weeks
|
Diet quality assessed using Healthy Eating Index (24 hour recall)
|
Change from baseline at 8 weeks
|
Father & child BMI/BMI Z-Score
Time Frame: Change from baseline at 8 weeks
|
Change from baseline at 8 weeks
|
|
Meals in Our Household questionnaire
Time Frame: Change from baseline at 8 weeks
|
Mealtime behaviors and practices including shopping, meal planning, cooking, family meals
|
Change from baseline at 8 weeks
|
Healthy Kids Questionnaire
Time Frame: Change from baseline at 8 weeks
|
Father and child nutrition behaviors including vegetable and sweetened beverage intake frequency & Physical activity behaviors including play and screen time
|
Change from baseline at 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Amy R Mobley, PhD, RD, University of Connecticut
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
December 31, 2018
Study Completion (Actual)
April 30, 2019
Study Registration Dates
First Submitted
February 26, 2017
First Submitted That Met QC Criteria
March 3, 2017
First Posted (Actual)
March 6, 2017
Study Record Updates
Last Update Posted (Actual)
June 5, 2019
Last Update Submitted That Met QC Criteria
June 4, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H15-338
- 1R21HD087817-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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