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N/A N=32 Treatment

App-Based Mindfulness Training for Individuals With Anorexia Nervosa and Bulimia Nervosa

Anorexia Nervosa · Bulimia Nervosa · Anorexia Nervosa, Atypical · Bulimia; Atypical

Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcome: Primary: Feasibility of Module Completion — 87.8 percentage of modules completed

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Mindful Courage (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Yeshiva University
Primary completion
Jan 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Feasibility of Module Completion
87.8
PRIMARY
Acceptability Dimensions
4.28
SECONDARY
Change in Eating Disorder Symptoms
-1.42
SECONDARY
Change in Emotion Dysregulation
-0.40
SECONDARY
Change in Body Dissatisfaction
-26.47
SECONDARY
Savoring Beliefs
1.30
SECONDARY
Psychosocial Impairment
-13.22
SECONDARY
Change in Mindfulness
0.33

Summary

We will evaluate the acceptability and feasibility of a 8-week long digital mindfulness-based intervention for anorexia nervosa and bulimia nervosa. This study is a prospective single-arm trial during the intervention development phase. Following this phase, after the intervention has been further developed, a subsequent study (with a different clinicaltrials.gov identification #) will utilize a randomized control trial design.

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Can read and write in English
  • Meet diagnostic DSM 5 diagnostic criteria for anorexia nervosa, bulimia nervosa, or atypical anorexia nervosa/bulimia nervosa
  • Owns a smartphone
  • Willing and able to participate in an eight-week long research study
  • Have a private quiet space at home or headphones to complete modules
  • Completed one month or more of eating disorder treatment
  • Currently enrolled in eating disorder treatment

Exclusion Criteria

  • Fail to meet above-listed inclusion criteria
  • Current alcohol or drug dependence
  • Current untreated psychotic or bipolar disorder
  • Current suicidal intent
  • Significant cognitive impairment that would impair the ability to use Mindful Courage effectively
  • BMI <15 or medically unstable
  • Currently receiving residential/inpatient treatment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05753410). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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