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

Primary Purpose

Obesity, Binge Eating

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Track clinician-determined symptoms
Track clinician-determined and self-determined symptoms
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Obesity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Condition 1

Condition 2

Arm Description

Track clinician-determined symptoms

Track clinician-determined and self-determined symptoms

Outcomes

Primary Outcome Measures

Compliance
Number of tracking entries completed
Satisfaction with tracking
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

Full Information

First Posted
January 13, 2021
Last Updated
February 25, 2021
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT04711577
Brief Title
Examining Self-tracking Behaviors in a Mobile Intervention for Binge Eating and Weight Management
Official Title
Examining Self-tracking Behaviors in a Mobile Intervention for Binge Eating and Weight Management
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 8, 2021 (Actual)
Primary Completion Date
February 11, 2021 (Actual)
Study Completion Date
February 11, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Binge Eating

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Condition 1
Arm Type
Experimental
Arm Description
Track clinician-determined symptoms
Arm Title
Condition 2
Arm Type
Experimental
Arm Description
Track clinician-determined and self-determined symptoms
Intervention Type
Behavioral
Intervention Name(s)
Track clinician-determined symptoms
Intervention Description
Participants will track clinician-determined symptoms
Intervention Type
Behavioral
Intervention Name(s)
Track clinician-determined and self-determined symptoms
Intervention Description
Participants will track clinician-determined symptoms and a self-determined symptom
Primary Outcome Measure Information:
Title
Compliance
Description
Number of tracking entries completed
Time Frame
3 weeks
Title
Satisfaction with tracking
Description
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
Time Frame
3 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

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

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