Skip to main content
Clinical Trials/NCT02496637
NCT02496637
Completed
Not Applicable

A Brief Appetite Awareness Intervention for Eating and Weight Regulation Among College Freshmen: A Randomized Clinical Trial

University of Minnesota1 site in 1 country130 target enrollmentAugust 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Minnesota
Enrollment
130
Locations
1
Primary Endpoint
Change in Appetite Awareness as assessed by the Interoceptive Awareness Questionnaire (appetite subscale)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The proposed study is a randomized clinical trial investigating the effects of a weight gain and eating dysregulation prevention intervention among college freshmen women. It will compare Appetite Awareness Training (AAT) to a standard nutritional education group and a no treatment control group. Appetite Awareness Training approach to increasing eating regulation through training individuals to eat in response to their appetite cues rather than external or emotional cues.

Detailed Description

All female freshmen students residing in the university dorms were recruited to participate in this study. After completing the baseline assessment, eligible participants were randomly assigned to one of the three arms. Those in the AAT condition received guided administration of AAT over the course of three weekly group sessions, with an additional booster session three weeks after completion (week 6). The standard treatment comparison group received four similarly timed group sessions of psychoeducational/nutrition information facilitated by a registered dietician. A manualized approach to administration of the intervention was created based on the AAT treatment and was strictly followed in order to standardize the implementation of the prevention groups. The no-treatment control group only participated in the assessments.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
October 1, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Incoming University of Minnesota Duluth freshmen women residing in on campus dormitories

Exclusion Criteria

  • Males, non-dormitory residing, non-freshmen.

Outcomes

Primary Outcomes

Change in Appetite Awareness as assessed by the Interoceptive Awareness Questionnaire (appetite subscale)

Time Frame: Baseline, 6 weeks, 4 months

Change in Body Weight measured in pounds

Time Frame: Baseline, 6 weeks, 4 months

Secondary Outcomes

  • Change in Body Image as assessed by the Satisfaction and Dissatisfaction with Body Parts Scale(6 weeks, 4 months)
  • Change in Weight Management self-efficacy as assessed by the Weight Efficacy Lifestyle Questionnaire(6 weeks, 4 months)

Study Sites (1)

Loading locations...

Similar Trials