Actively Recruiting

Age: 18Years +
All Genders
NCT06790030

Does Self-Efficacy at the Start of Treatment Influence Treatment Outcome in Patients With EDs?

Led by Altrecht · Updated on 2025-01-23

50

Participants Needed

1

Research Sites

139 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to contribute to the improvement of treatment for eating disorders, by identifying factors that might positively affect treatment outcome. The main questions it aims to answer are: 1. Do higher levels of self-efficacy positively predict a more positive treatment outcome? 2. Does self-efficacy in itself improve during treatment? 3. Do autonomous motivation, self-esteem and self-efficacy correlate? These factors will be measured in patients being treated for their eating disorders with Cognitive Behavior Therapy - Ten (CBT-T). Researchers will administer questionnaires at start, session four and end of treatment. Participants will: 1. Receive their treatment as usual. 2. fill in questionnaires at the start of treatment, session 4 and end of treatment.

CONDITIONS

Official Title

Does Self-Efficacy at the Start of Treatment Influence Treatment Outcome in Patients With EDs?

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be 18 years or older
  • Have an eating disorder diagnosed according to the Diagnostic Statistical Manual (DSM-5)
  • Starting CBT-T treatment
Not Eligible

You will not qualify if you...

  • Intellectual disability according to the Diagnostic Statistical Manual (DSM-5) or an IQ below 80
  • Inability to speak or read Dutch
  • Patients treated under a legal act

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Altrecht Eatings Disorders Rintveld

Zeist, Utrecht, Netherlands, 3705WE

Actively Recruiting

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Research Team

A

Alberte Jansingh, MSc

CONTACT

U

Unna Danner, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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