Relase prevention via videoconference after inpatient care in anorexia nervosa - a pilot study

Not Applicable

• Conditions: F50.0; Anorexia nervosa

• Registration Number: DRKS00003476
• Lead Sponsor: niversitätsklinikum Tübingen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-01-05
• Study Completion: 2015-09-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 16

Inclusion Criteria

Full-syndrom or subsyndromal Anorexia nervosa according to ICD-10 (F50.0 or F50.1) at admission to inpatient treatment, regular completion of inpatient treatment, written informed consent

Exclusion Criteria

Severe somatic disorder, current substance dependance, psychosis, current suicidal crisis, pregnancy or lactation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
need for, feasability and acceptance of the intervention<br><br>The primary endpoint will be assessed by interviews and self-report instruments at the end of intervention (4 months after beginning of the intervention).

Secondary Outcome Measures

Name	Time	Method
relapse rate, health care utilization<br><br>The secondary endpoint will be assessed by weight measurement, interviews and self-report instruments at the end of intervention (4 months after beginning of the intervention).