Purpose

The goal of this study is to develop and test a digital program to help people with eating disorders in their everyday lives. The program uses brief surveys and sensor data collected by smartphones to understand when someone may be at higher risk for behaviors like restricting food, binge eating, or using unhealthy weight control behaviors.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 70 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Age 18-70 2. At least 12 ED behaviors from the same behavioral category in the past 12 weeks (i.e., at least 12 binge eating episodes, at least 12 compensatory behaviors, and/or at least 12 instances of dietary restriction) 3. Ownership of a smartphone 4. Willingness to complete ecological momentary assessment (EMA) and sensor data collection 5. Live in the United States 6. Has a primary care provider or is willing to establish a primary care provider

Exclusion Criteria

  1. Inability to fluently speak, read, and write in English 2. Body mass index < 17.5 kg/m2 3. Medical complications of ED symptoms requiring immediate treatment 4. Current ED-focused therapy 5. Severe psychopathology (i.e., active suicidal ideation, psychosis, bipolar disorder, or substance use disorder) or intellectual disability inhibiting engagement in study protocols

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Intervention Model Description
The study involves a micro-randomized trial design, in which participants will all receive just-in-time adaptive interventions, the content of which will be micro-randomized (i.e., randomized in the moment of delivery). Participants will not be assigned to groups at the start of the trail but instead will be assigned a specific just-in-time adaptive intervention (or no intervention) randomly at each instance when they are at elevated risk for eating disorder behaviors. All participants may receive all types of just-in-time adaptive interventions during the course of the study, but the order of receipt (and the specific timing of receipt) will vary between participants.
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
All Participants Receive Just-In-Time Adaptive Interventions (JITAIs) through the EDDI App
All participants will receive just-in-time adaptive interventions when their personalized model identifies that they are at risk for an eating disorder behavior. The content of the just-in-time adaptive intervention (i.e., the therapy skill targeted) will be randomized at the point of just-in-time adaptive intervention delivery.
  • Behavioral: Eating Disorder Dynamic Intervention
    Participants will use a smartphone-based program designed to support eating disorder recovery in daily life. Participants will complete brief surveys about their mood, thoughts, and behaviors, and the smartphone will also passively collect activity-related data. This information is used to detect times when a person may be at higher risk for eating disorder behaviors. Participants will watch 4 video modules that introduce the core enhanced cognitive-behavioral therapy skills for eating disorders (reducing dietary restraint, urge management, emotion regulation, and improving body image), provide rationale, and prompt participants to complete interactive activities to practice these skills. Participants will then receive micro-randomized JITAIs prompting them to use these skills in their daily lives; micro-randomization will be used to deliver a JITAI from one of the 4 skill categories (reducing dietary restraint, urge management, emotion regulation, improving body image) or no JITAI.

Recruiting Locations

Dartmouth College
Lebanon, New Hampshire 03766
Contact:
Emily K Presseller, PhD
603-646-7109
eddi.project@dartmouth.edu

More Details

Status
Recruiting
Sponsor
Trustees of Dartmouth College

Study Contact

Emily K Presseller, PhD
(203) 974-2949
emily.k.presseller@dartmouth.edu

Detailed Description

In this study, 170 adults with eating disorders will take part. They will regularly report on their thoughts, feelings, and behaviors throughout the day. Based on this information, the program will send "just-in-time" support, which involves short, tailored suggestions that encourage the use of helpful coping skills right when they are most needed. The study has three main goals: 1. To better understand risk patterns: The investigators will use real-time data to build personalized models that predict when someone is at higher risk for eating disorder behaviors based on their own data and patterns. 2. To test which therapy skills work best and why: The investigators will examine how different evidence-based therapy skills (such as managing urges, improving mood, reducing strict dieting, and improving body image) help reduce eating disorder behaviors in daily life, and what psychological factors explain these effects. 3. To evaluate the program's usability: The investigators will assess whether participants find the digital support helpful, easy to use, and acceptable in their daily routines.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.