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Cognitive Remediation Therapy in Anorexia nervosa - a randomized controlled trial

Cognitive Remediation Therapy in Anorexia nervosa - a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00006870
Enrollment
168
Registered
2015-02-17
Start date
2015-06-02
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 F50.1

Interventions

Group 1: Treatment as usual (TAU) + Cognitive Remediation Therapy (CRT) for AN (group format, 1 session per week, 100 min. each, over 10 weeks) *CRT belongs to the so-called neurobehavioral treatment

Sponsors

Klinik Lüneburger Heide
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to No maximum

Inclusion criteria

Inclusion criteria: DSM-V diagnosis of AN, indication for inpatient treatment

Exclusion criteria

Exclusion criteria: acute life-threatening conditions; medical instability; severe psychiatric comorbidity (i.e. schizophrenia, bipolar disorder, organic mental disorder)

Design outcomes

Primary

MeasureTime frame
Body Mass Index, total score in the Eating Disorder Examination Questionnaire and total score in the Eating Disorders Quality of Life Questionnaire 6 months after treatment

Secondary

MeasureTime frame
Body Mass Index, total score in the Eating Disorder Examination Questionnaire and total score in the Eating Disorders Quality of Life Questionnaire 10 weeks after first treatment session; cognitive flexibility as assessed by the Wisconsin Card Sorting Test, the Trail Making Test and the Detail and Flexibility Questionnaire 10 weeks after first treatment session; Drop-out rate 10 weeks after first treatment session; treatment acceptance as measured by an evaluation form 10 weeks after first treatment session

Countries

Germany

Contacts

Public ContactWally Wünsch-Leiteritz

Klinik Lüneburger Heide

wuensch-leiteritz@klinik-lueneburger-heide.de+49 5821 960 0

Outcome results

None listed

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