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Clinical Trials/NCT02076854
NCT02076854
Completed
Not Applicable

A Novel Motivational Ecological Momentary Intervention for Anorexia Nervosa

Boston University1 site in 1 country12 target enrollmentOctober 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Eating Disorders
Sponsor
Boston University
Enrollment
12
Locations
1
Primary Endpoint
Change in Motivation to Change Eating Disorder Behaviors
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of this study is to pilot an innovative motivational text-message intervention for individuals with anorexia nervosa and subthreshold anorexia nervosa. Patients will receive personalized motivational text-messages as an adjunct to cognitive behavioral therapy (CBT). CBT will be provided to patients at no cost for the duration of the study. The investigators hypothesize that the text-messages will help increase motivation to change and kilocalorie intake and decrease eating disordered behavior.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
February 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Anorexia nervosa/subthreshold anorexia nervosa (i.e., individuals who exhibit significant dietary restraint)
  • 18+ years old

Exclusion Criteria

  • BMI \< 16.5
  • Medication instability for 6 weeks
  • Recent/current suicidal risk
  • Comorbid substance abuse or dependence, bipolar disorder, schizophrenia, or mental retardation
  • Inability to provide release of information to a medical provider

Outcomes

Primary Outcomes

Change in Motivation to Change Eating Disorder Behaviors

Time Frame: Daily for 8 weeks

Change in Eating Disorder Symptoms

Time Frame: Daily for 8 weeks

Kilocalorie Intake (measured by self-report food records)

Time Frame: Daily for 8 weeks

Secondary Outcomes

  • Feasibility measured by compliance with daily questionnaire(8 weeks)
  • Acceptability measured by self-report ratings(8 weeks)

Study Sites (1)

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