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NCT02206191 Clinical Trial

The Primary Care Obesity Network (PCON): Incorporating Principles of Self-regulation of Intake

Self-regulation Clinical Trial

— PCON  

Official title:
The Primary Care Obesity Network (PCON): Incorporating Principles of Self-regulation of Intake

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02206191
Other study ID # IRB13-00262
Secondary ID Food Innovation
Status Completed
Phase
First received July 21, 2014
Last updated March 29, 2018
Start date July 2013
Est. completion date January 30, 2017

Study information
Verified date March 2018
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date January 30, 2017
Est. primary completion date January 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Mother of a 6-11 year old child

Exclusion Criteria:

- Unable to speak and read English

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (2)
Lead Sponsor Collaborator
Nationwide Children's Hospital Ohio State University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Examining use of disordered self-regulatory feeding behaviors, at survey completion At survey completion, which will occur about 30 minutes after the survey is administered
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