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Online Relapse Prevention Study

A Pilot Randomized Control Trial of a Relapse Prevention Online Exposure Protocol for Eating Disorders and Mechanisms of Change

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04862247
Acronym
ORP
Enrollment
130
Registered
2021-04-27
Start date
2021-06-04
Completion date
2025-02-01
Last updated
2025-03-30

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

Conditions

Anorexia Nervosa, Anorexia Nervosa, Atypical, Bulimia Nervosa, Eating Disorders, Other Specified Feeding or Eating Disorder

Keywords

Relapse Prevention, Treatment, Eating Disorder Symptoms, Therapy

Brief summary

The purpose of this study is to collect preliminary data on the feasibility and acceptability of the randomization of two relapse-prevention treatment conditions after discharge from intensive eating disorder (ED) treatment: an imaginal exposure therapy and a writing and thinking intervention. The second aim to test for (a) differences between the two treatments for the prevention of relapse and (b) preliminary change on clinical ED outcomes (e.g., ED symptoms, fears). The investigators further aim to examine the two treatments target fear extinction and if fear extinction is associated with ED outcomes. The investigators also plan to test if baseline differences in fear conditioning relate to change in ED outcomes across treatment.

Interventions

BEHAVIORALImaginal Exposure Condition

Participants will be asked to think and write about an eating related fear or anxiety. Specifically, they will be asked to spend 20-30 minutes writing about a specific fear or anxiety they have, then another 20-35 minutes re-reading and imagining that what they have written is happening.

BEHAVIORALWriting and Thinking Condition

Participants will be asked to think and write about their eating disorder using specific prompts designed to help them process their eating disorder. Specifically, they will be asked to spend 20-30 minutes writing their eating disorder, then another 20-35 minutes re-reading what they wrote.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
King's College London
CollaboratorOTHER
University of Louisville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* over the age of 18 * discharged from intensive treatment within the last four months (inpatient, residential, partial hospital/day program, intensive outpatient program) * currently meet criteria for anorexia nervosa, other specified feeding and eating disorder-atypical anorexia nervosa, or bulimia nervosa

Exclusion criteria

* high and active suicidality, psychosis, mania, or medical compromised status will be excluded, as these comorbidities would make it difficult to complete study procedures * under the age of 18 * does not meet criteria for anorexia nervosa, other specified feeding and eating disorder-atypical anorexia nervosa, or bulimia nervosa. * discharged from intensive treatment more than four months ago

Design outcomes

Primary

MeasureTime frameDescription
Rate of Eating Disorder Relapse6-Month Follow-UpFirst, the investigators will define relapse as moving from one stage of remission to another (e.g., remission to partial remission or partial remission to currently ill). Second, the investigators will define relapse as re-entry into a more intensive treatment setting (e.g., moving from outpatient to partial hospitalization).
Change in Eating Disorder Symptoms using the EDE-QUp to 6-Month Follow-UpThe Eating Disorder Examination Questionnaire (EDEQ), a self-reported measure, is assessed at multiple time points throughout the duration of the study and is used to examine the attitudes and behaviors in individuals with eating disorder symptoms.
Re-admission Percentage1 Month Follow Up and 6 Month Follow UpUsing the Treatment Interview, we will assess all current and past treatment experiences, dates of treatment, and primary type of treatment. Re-admission will be assessed at follow up timepoints and defined as re-entry into a more intensive treatment setting.

Secondary

MeasureTime frameDescription
Change in Eating Disorder SymptomsTreatment Session 2 through 5Eating Disorder-15 is a 15-item measure of eating disorder cognitions and behaviors, which will be collected at the beginning of each treatment session.
Change in State AnxietyTreatment Session 1 through 5Subjective Units of Distress(SUDS) is a valid and reliable behavioral measure of state anxiety used during each treatment session to measure anxiety and distress and will be collected before, during, and after each session. Additionally, the Brief State Anxiety Measure is a 6-item measure with acceptable reliability and validity and sensitivity to fluctuations in state anxiety levels and will be collected at the beginning and end of each session.
Fear ExtinctionUp to 6 Month Follow UpFLARe is a validated smart-phone behavioral assessment of fear learning that will assess target engagement at baseline, post, and one and six month follow-ups.
Change in State Fear of FoodTreatment Session 2 through 5State Fear of Food Measure will be used to assess food anxiety, food avoidance, and feared concerns and will be collected at the beginning and end of each session.
Change in Positive and Negative AffectTreatment Session 2 through 5State Positive and Negative Affect Schedule will be used to assess positive and negative affect at the beginning and end of each session.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026