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A Novel Motivational Ecological Momentary Intervention for Anorexia Nervosa

A Novel Motivational Ecological Momentary Intervention for Anorexia Nervosa

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02076854
Enrollment
12
Registered
2014-03-04
Start date
2013-10-01
Completion date
2015-02-01
Last updated
2026-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Disorders

Keywords

eating disorders, anorexia nervosa, treatment, technology

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.

Interventions

BEHAVIORALText-Message Intervention

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Change in Motivation to Change Eating Disorder BehaviorsDaily for 8 weeks
Change in Eating Disorder SymptomsDaily for 8 weeks
Kilocalorie Intake (measured by self-report food records)Daily for 8 weeks

Secondary

MeasureTime frame
Feasibility measured by compliance with daily questionnaire8 weeks
Acceptability measured by self-report ratings8 weeks

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRebecca Shingleton, M.A.

Boston University Charles River Campus

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026