Eating Disorder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
Exclusion criteria
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).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary treatment outcome measure is the post treatment Eating Disorder level. This is assessed with the SCID-I. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary treatment outcome measures are the level of eating disorder pathology (EDE-Q), the presence of common mental disorders (WSQ), self-esteem (RSE/ IAT), perfectionism (F-MPS), interpersonal problems (IPP-32) and anxiety and depression symptoms (MASQ). The cost-effectiveness measures are health related quality of life (EQ-5D and SF-36), service receipt and productivity losses (TiC-P; SF-HLQ), including use of mental and primary health care, social services, out-of-pocket expenditures, travel costs and waiting time (TiC-P; SF-HLQ). The CarerQoL is used to measure and value the subjective burden of informal care in terms of well-being. | — |
Countries
Netherlands