Emotion Focused Internet Delivered Treatment for Adults with Eating Disorders

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-02

Study Completion Date

2024-06-01

Brief Summary

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The goal of this clinical trial is to develop and test a new internet delivered treatment for adult patients with eating disorders, focused on developing normalized eating patterns and emotion regulation skills. The main focus is to investigate the additional effect of emotion regulation interventions, beyond the effect of other central tratment components normally included in evidence based eating disorder treatment.

The internet delivered treatment is divided into two phases, phase A and phase B. Phase A focus on establishing normalised eating patterns, and in phase B the emotion regulation interventions are added. Participants will get access to treatment modules every third day over a time period of 8.5 weeks, each module consist of psychopedagogical material, excercises and home work.

Data will be collected via the online research platform every third day during the treatment. Data is also collected at more comprehensive assessment points pre-treatment, post-treatment, and follow up 3 months after end of treatment.

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Detailed Description

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This study uses an experimental single-case design, specifically a randomized replicated AB design.

The baseline lenght (i.e., phase A) is randomized for each participant. There is six possible assignments, as the randomization is restricted to give all participants minimum 8 and maximum 12 treatment modules in each phase, with minimum 9 and maximum 14 baseline assessment points.

Conditions

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Eating Disorders

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

A single-case experimental randomized AB-design. Baseline length (i.e., phase A) and start of the B-phase is randomized for each participant. Both phases consist of active treatment, with the purpose of investigating if the interventions added in phase B could enhance treatment results additionally beyond the interventions given during the baseline period.

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Emotion regulation treatment

Group Type EXPERIMENTAL

Emotion regulation treatment

Intervention Type BEHAVIORAL

Emotion regulation intervention in two phases. Phase A focus on establishing normalised eating patterns, and in phase B the emotion regulation interventions are added. Participants will get access to treatment modules every third day over a time period of 8.5 weeks, each module consist of psychopedagogical material, excercises and home work.

Interventions

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Emotion regulation treatment

Emotion regulation intervention in two phases. Phase A focus on establishing normalised eating patterns, and in phase B the emotion regulation interventions are added. Participants will get access to treatment modules every third day over a time period of 8.5 weeks, each module consist of psychopedagogical material, excercises and home work.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* DSM5 eating disorder
* Minimum 18 years old
* Ongoing contact with a psychiatric clinic in sweden

Exclusion Criteria

* Body mass index below 18,5
* Somatic instability due to eating disorder severeness
* High risk of suicide or severe self-harm
* Ongoing addiction or substance abuse
* Ongoing psychological treatment or psychotherapy
* New or changed mediciation for psychiatric disorders in the past 2 months
* Planned or ongoing pregnancy or recently gave birth

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No