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Evaluation of an impulsivity-focused group intervention in clinical practice for patients with binge eating disorder

Evaluation of an impulsivity-focused group intervention in clinical practice for patients with binge eating disorder - IMPULS in clinical practice

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025697
Enrollment
40
Registered
2021-06-28
Start date
2021-06-18
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

DSM-5 Binge Eating Disorder F50.9

Interventions

Group 1: treatment group: Patients with binge eating disorder who participate in a impulsivity-focused group treatment (9-14 sessions a 60-90 min in biweekly rhythm)

Sponsors

Universitätsklinikum Tübingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of BED; participation on the outpatient IMPULS treatment; informed written consent

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Primary outcomes are feasability and acceptance of the outpatient IMPULS treatment, that will be assessed by the rate of recruitment, drop-out rate, extent of participation in the sessions, extent of homework done, subjective evaluation of patients, subjective evaluation of therapists. We assess primary outcomes depending on the frequency of participated sessions and type of session (digital vs. face to face format).

Secondary

MeasureTime frame
Secondary outcomes are time effects between T0 and T1 concerning the effectivity of the outpatient IMPULS treatment, in particular the frequency of binge eating episodes in the last four weeks according to EDE-Q. Other secondary outcomes comprise time effects between T0 and T1 concerning eating disorder pathology (EDE-Q), depression (BDI II), impulsive eating behaviour (TFEQ, process analyses, work sheets, eating-related self efficacy) and impulsivity (BIS-15). We assess secondary outcomes depending on the frequency of participated sessions and type of session (digital vs. face to face format).

Countries

Germany

Contacts

Public ContactKathrin Schag

Universitätskliniukum TübingenPsychosomatische Medizin & Psychotherapie

kathrin.schag@med.uni-tuebingen.de07071-29-89117

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 27, 2026