Examining the impact of self-efficacy on treatment outcomes for eating disorders
Does Self-Efficacy at the Start of Treatment Predict Treatment Outcome in Patients With EDs?
This study is trying to see if feeling more confident in themselves helps people with eating disorders do better in treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Altrecht Academic / other |
| Locations | 1 site (Zeist, Utrecht) |
| Trial ID | NCT06790030 on ClinicalTrials.gov |
What this trial studies
This observational study aims to improve treatment outcomes for patients with eating disorders by investigating the role of self-efficacy at the start of treatment. It will assess whether higher levels of self-efficacy predict better treatment outcomes and whether self-efficacy improves during the course of treatment. Participants will undergo Cognitive Behavior Therapy - Ten (CBT-T) and complete questionnaires at the beginning, during, and at the end of their treatment. The study will also explore correlations between self-efficacy, autonomous motivation, and self-esteem.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have a diagnosed eating disorder and are starting CBT-T treatment.
Not a fit: Patients with intellectual disabilities, those unable to communicate in Dutch, or those under legal treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to enhanced treatment strategies that improve recovery outcomes for patients with eating disorders.
How similar studies have performed: Previous studies have indicated that self-efficacy is a significant predictor of treatment outcomes in eating disorders, suggesting that this approach is supported by existing research.
Eligibility criteria
Show full inclusion / exclusion criteria
Patients are eligible for participation when they meet the following inclusion criteria: * Participants must be 18 years or older * Having an eating disorder diagnosed according to the Diagnostic Statistical Manual (DSM-5) * Starting CBT-T treatment Exclusion criteria * 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
Where this trial is running
Zeist, Utrecht
- Altrecht Eatings Disorders Rintveld — Zeist, Utrecht, Netherlands (Recruiting)
Study contacts
- Study coordinator: Alberte Jansingh, MSc
- Email: a.jansingh@altrecht.nl
- Phone: +31306965477
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.