- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05773157
Evaluation of SNAP-Ed Online Modules to Improve Responsive Feeding Practices of Caregivers
Study Overview
Detailed Description
the Center for Childhood Obesity Research developed three online modules for caregivers of children ages 5-12 years old who are participating in SNAP-Ed programming. These modules were developed to be used within the context of normal programming that participants will receive in any given year. The specific aim are as follows:
Aim #1: To examine acceptability of these modules by caregivers participating in SNAP-Ed programming. This will be assessed by evaluating acceptability questions answered by participants after completing the modules.
Aim #2: To examine the feasibility of these modules by caregivers participating in SNAP-Ed programming, assessed by >60% completion rate of all three modules.
Online module content will focus on topics such as:
- Shared Responsibility of Feeding:
- Parent Provides, Child Decides
- Family Mealtimes
- Hunger and Fullness
- Avoiding use of controlling feeding practices
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
University Park, Pennsylvania, United States, 16802
- Penn State
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Primary caregiver of a child between the ages of 2 to 16 years
- Over the age of 18
- English-speaking
- Have a reliable internet source and active email account so they can access the online modules
Exclusion Criteria:
- Are not the primary caregivers of a child between the ages of 2 to 16 years
- Are under the age of 18
- Are not English-speaking
- Do not have a reliable internet source or email address
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Receive Online Modules
All participants receiving the same online modules intervention.
|
Participants receive modules to improve responsive feeding practices of caregivers
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feeding Practices
Time Frame: 1 month
|
Pre/post Feeding Practices surveys
|
1 month
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00020516
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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