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Examining Self-tracking Behaviors in a Mobile Intervention for Binge Eating and Weight Management

Not Applicable
Completed
Conditions
Obesity
Binge Eating
Interventions
Behavioral: Track clinician-determined symptoms
Behavioral: Track clinician-determined and self-determined symptoms
Registration Number
NCT04711577
Lead Sponsor
Northwestern University
Brief Summary

The purpose of this study is to understand users' experiences and interests completing self-tracking in a mobile intervention for binge eating and weight management.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Adults age 18 years or older
  • Obesity (BMI ≥30)
  • Recurrent binge eating (≥12 episodes in the past 3 months)
  • Interested in losing weight and reducing binge eating
  • Willing to use a mobile application
  • Willing to practice self-monitoring
  • Has access to a scale
  • Not pregnant
  • English-speaking
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Condition 1Track clinician-determined symptomsTrack clinician-determined symptoms
Condition 2Track clinician-determined and self-determined symptomsTrack clinician-determined and self-determined symptoms
Primary Outcome Measures
NameTimeMethod
Compliance3 weeks

Number of tracking entries completed

Satisfaction with tracking3 weeks

Self-reported satisfaction with tracking, based on the Satisfaction subscale of the Usefulness, Satisfaction, and Ease of use (USE) Questionnaire, with higher scores on the 1-7 rating scale indicating greater satisfaction

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Northwestern University

🇺🇸

Chicago, Illinois, United States

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