F50 F33 F60 F40 F41 F42 F43 F44 F45 F34 F32
Conditions
Interventions
Group 1: One-to-one sessions and group therapy of 12 week inpatient setting
specific cognitive interventions to change overevaluation of shape, weight and their control according to the individual for
cognitive concept
dieting as a typical core problem due to low self-esteem
joined information on eating disorder specific themes
high individualization of the therapy
Group 2: One-to-one sessions and group therapy of 12 week inpatient setting
focus on relation of emotional regulation and eating behavior
dysfunctional emotion regulation as core problem
dialectical strategies (balance of acceptance and change, validation, commitment strategies, pro/cons lists)
mealtime as mindfulness exercise
joined information
systematic skills training
limited individualization
Group 3: wait control group: treatment-as-usual, e.g. practical doctor
Sponsors
Universitätsklinikum Schleswig-Holstein Campus Lübeck
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Eating Disorder Examination Questionnaire (EDE-Q) Borderline Symptom List (BSL) Questionnaire on general health status (SF-12) Diagnosis (ICD-10) Brief Symptom Inventory (BSI) Quick Inventory of Depressive Symptomatology (QIDS) Anxiety (HADS-D) Emotion regulation questionaires (ICARUS, DERS, ERQ) metabolic parameter: cortisol profile, biometrical data pre, pre II, start of the treatment, end of the treatment, post (3 months after end), follow-up (9 months after end) | — |
Countries
Germany
Contacts
Public ContactSibylle Grell
psychiatrische Hochschulambulanz des UKSH, Campus Lübeck
Outcome results
None listed