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Psychological treatment of Eating Disorders: A multi-centered randomized controlled trial on the (cost-)effectiveness of Enhanced Cognitive Behavior Therapy (CBT-E) Titel for patients: Effectiveness study on the therapy of eating disorders

Phase 3
Recruiting
Conditions
Eating Disorder
10014067
Registration Number
NL-OMON39403
Lead Sponsor
Parnassia Bavo Groep (Den Haag)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
140
Inclusion Criteria

Adult outpatients (from age 18) with an ED diagnosis, AN, BN, EDNOS (SCID-I, with additional proposed DSM-5 criteria for BED) and a 17.5 < BMI <40

Exclusion Criteria

The patients who will be excluded will be those whose current clinical state or circumstances make it inappropriate for them to enter treatment experiment (e.g., those at high medical or suicidal risk, psychoses), or patients who are not available for the coming 20 weeks. (For specific exclusion criteria see Research Protocol page 15).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary treatment outcome measure is the post treatment Eating Disorder<br /><br>level. This is assessed with the SCID-I. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary treatment outcome measures are the level of eating disorder pathology<br />(EDE-Q), the presence of common mental disorders (WSQ), self-esteem (RSE/ IAT),<br />perfectionism (F-MPS), interpersonal problems (IPP-32) and anxiety and<br />depression symptoms (MASQ). The cost-effectiveness measures are health related<br />quality of life (EQ-5D and SF-36), service receipt and productivity losses<br />(TiC-P; SF-HLQ), including use of mental and primary health care, social<br />services, out-of-pocket expenditures, travel costs and waiting time (TiC-P;<br />SF-HLQ). The CarerQoL is used to measure and value the subjective burden of<br />informal care in terms of well-being.</p>
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