Impact of a Mobile App-Based Waitlist Intervention (MI-Coach: ED) on Readiness for Eating Disorder Treatment: A Randomized Controlled Trial
Sponsor: University of British Columbia
Trial Details
| Condition | Eating Disorders |
| Intervention | MI-Coach: ED Mobile App |
| Phase | NA |
| Status | Recruiting |
| Participants | 74 |
| Est. Completion | 1 June 2027 |
| Last Updated | 8 May 2026 |
Primary Outcome
Change from Baseline in Overall Motivation for Treatment as Measured by the Readiness and Motivation Questionnaire (RMQ) at 4 Weeks; Rate of Change in Weekly Motivation Levels as Measured by the Motivational Stages of Change for Adolescents Recovering from an Eating Disorder (MSCARED) During the Initial 4 Weeks; Change from Baseline in Confidence to Engage in Treatment as Measured by the Confidence Subscale of the Readiness and Motivation Questionnaire (RMQ) at 4 Weeks
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Must self-identify as a woman, including cisgender or transgender individuals. * Must be at least 18 years old at the time of enrollment. * Currently on a waitlist to receive treatment for an eating disorder at provincially funded eating disorder programs in British Columbia. * Meets criteria for a threshold or subthreshold eating disorder, including anorexia nervosa (restricting or binge/purge subtype), bulimia nervosa, binge eating disorder, or other specified feeding or eating disorder (OSFED). * Able to read and understand English fluently. * Owns or has regular access to a smartphone or mobile device capable of running the MI-Coach: ED app. Exclusion Criteria: * Does not identify as a woman, regardless of sex assigned at birth. * Currently receiving active treatment for an eating disorder, such as outpatient therapy, inpatient care, or day programs. * Diagnosed with a schizophrenia-spectrum disorder or other psychotic disorder. * Presence of a cognitive impairment or sensory deficit (e.g., severe visual or hearing impairment) that would interfere with the ability to use the app or complete study assessments. * History of a recent traumatic brain injury or neurological condition that might impact participation. * Any condition that, in the opinion of the investigators, would interfere with the participant's ability to comply with the study protocol or complete the intervention.
Trial Sites
Countries
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