- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02206191
The Primary Care Obesity Network (PCON): Incorporating Principles of Self-regulation of Intake (PCON)
March 29, 2018 updated by: Ihuoma Eneli, Nationwide Children's Hospital
In response to the high prevalence rates of childhood obesity in central Ohio, the Center for Healthy Weight and Nutrition (CHWN) established the Primary Care Obesity Network (PCON); a partnership between primary care physicians and Nationwide Children's Hospital's Center for Healthy Weight and Nutrition, a tertiary care obesity center, the first of its kind in Ohio.
The overall goal of PCON is to bring an effective and user friendly obesity management program to the community physician's office to prevent and treat the growing number of obese children in the setting of the private office.
The predominant nutrition messaging approach to tackling childhood obesity has revolved around the food choices and portion sizes.
While this is relevant, an area with significant potential for impact for maintaining optimal growth and a healthy weight for young children is addressing feeding behaviors and self-regulation of intake;.
- the "how" of eating.
The investigators objective it to investigate whether this self-regulation approach can be employed for an older age group of 6-11 years old.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
120
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
-
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Ohio
-
Columbus, Ohio, United States, 43205
- Nationwide Children's Hospital
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Mothers of 6-11 year olds being seen in primary care offices throughout Columbus, OH.
Description
Inclusion Criteria:
- Mother of a 6-11 year old child
Exclusion Criteria:
- Unable to speak and read English
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
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Mothers of 6-11 year olds
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Examining use of disordered self-regulatory feeding behaviors, at survey completion
Time Frame: At survey completion, which will occur about 30 minutes after the survey is administered
|
At survey completion, which will occur about 30 minutes after the survey is administered
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: ihuoma Eneli, MD, Nationwide Childrens Hospital, Columbus, Ohio
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
July 1, 2013
Primary Completion (Actual)
January 30, 2017
Study Completion (Actual)
January 30, 2017
Study Registration Dates
First Submitted
July 21, 2014
First Submitted That Met QC Criteria
July 31, 2014
First Posted (Estimate)
August 1, 2014
Study Record Updates
Last Update Posted (Actual)
March 30, 2018
Last Update Submitted That Met QC Criteria
March 29, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB13-00262
- Food Innovation Center (Other Grant/Funding Number: The Ohio State University)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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