Skip to main content
Clinical Trials/NCT04531436
NCT04531436
Completed
Not Applicable

Testing a Brief Mindful Eating Program: Feasibility and Proof of Concept

McGill University1 site in 1 country68 target enrollmentSeptember 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Overeating
Sponsor
McGill University
Enrollment
68
Locations
1
Primary Endpoint
Change in overeating
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This project evaluated the effects of a brief manualized mindful eating intervention as a treatment for overeating with individuals with overweight and obesity.

Detailed Description

Overeating leads to overweight and obesity. Effective eating regulation largely depends on an individual's responsiveness to internal cues of physiological hunger and satiety; this phenomenon is known as interoceptive awareness and has been shown to be lower in individuals with overweight or obesity. Mindfulness training may improve interoceptive awareness and thus may facilitate more effective regulation of eating through increased sensitivity to cues of hunger and fullness. Mindful eating programs have been shown to increase interoceptive awareness of hunger and satiety cues and decrease weight in individuals with obesity. Although these programs are effective, they involve lengthy group sessions, require extensively trained staff, and are not widely available outside of clinical research. Thus, the reach and impact of these programs are limited. The present study developed and tested a brief mindful eating intervention inspired by Kristeller \& Wolever's (2010) Mindfulness-Based Eating Awareness Training program to increase interoceptive awareness in individuals with overweight and obesity as a means to increase mindful and intuitive eating, reduce overeating and facilitate weight loss. The program consisted of 9 weekly 10-15 minute sessions structured around one simple evidence-based mindful eating exercise, and was delivered to adult (ages 18-67) employees from a Canadian university.

Registry
clinicaltrials.gov
Start Date
September 1, 2017
End Date
September 1, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Barbel Knauper

James McGill Professor

McGill University

Eligibility Criteria

Inclusion Criteria

  • BMI of 25 to 45 kg/m2 (overweight/obese)
  • Willingness to commit to program and complete various assessment measures

Exclusion Criteria

  • Having been pregnant in the past six months or planning on becoming pregnant in the next year
  • Undergoing treatment for cancer
  • Using medications that affect body weight or appetite
  • Being diagnosed with bulimia nervosa, binge-eating disorder, major depressive disorder, or another severe psychiatric disease (including dementia)

Outcomes

Primary Outcomes

Change in overeating

Time Frame: Baseline, week 9, and 24-week follow-up

As measured by the Overeating Questionnaire. Scores can range from 0 to 40, with higher scores indicating a greater tendency to overeat

Secondary Outcomes

  • Change in body weight(Baseline, week 9, and 24-week follow-up)

Study Sites (1)

Loading locations...

Similar Trials