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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00003476
Enrollment
16
Registered
2012-01-05
Start date
2012-08-02
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F50.0

Interventions

Group 1: AN patients receive 10 sessions of a manualized relapse prevention (based on cognitive-behavioral therapy) after discharge from inpatient treatment via videoconferencing.

Sponsors

Universitätsklinikum Tübingen
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
need for, feasability and acceptance of the intervention 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

MeasureTime frame
relapse rate, health care utilization 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).

Countries

Germany

Contacts

Public ContactKatrin Giel

Universitätsklinikum Tübingen

katrin.giel@med.uni-tuebingen.de+ 49 7071 2986719

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026