Efficacy of CBT-E and DBT-E in the treatment of eating disordered patients with high comorbidity

Not Applicable

• Conditions: F50; F33; F60; F40; F41; F42; F43; F44; F45; F34

• Registration Number: DRKS00000519
• Lead Sponsor: niversitätsklinikum Schleswig-Holstein Campus Lübeck

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2010-10-07
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 398

Inclusion Criteria

Main inclusion criterion is the diagnosis an eating disorder, indication for inpatient treatment (e.g. failed outpatient treatment, high psychosocial impairment, conditions unfavourable to treatment in the immediate environment) in combination with every possible form of comorbidity. Further inclusion criteria are being female, age above 18 years, and first treatment in our hospital.

Exclusion Criteria

Patients who are not able to receive a psychotherapeutic treatment (dementia, psychosis) are excluded. Furthermore, substance abuse as the dominant present diagnosis is excluded.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome is the remission of the eating disorder assessed by EDE three months after the end of treatment (EDE-Score within one standard deviation of population mean).

Secondary Outcome Measures

Name	Time	Method
Eating Disorder Examination Questionnaire (EDE-Q)<br>Borderline Symptom List (BSL)<br>Questionnaire on general health status (SF-12)<br>Diagnosis (ICD-10)<br>Brief Symptom Inventory (BSI)<br>Quick Inventory of Depressive Symptomatology (QIDS)<br>Anxiety (HADS-D)<br>Emotion regulation questionaires (ICARUS, DERS, ERQ)<br>metabolic parameter: cortisol profile, biometrical data<br><br>pre, pre II, start of the treatment, end of the treatment, post (3 months after end), follow-up (9 months after end)