VIADUKT-I 6-month lifestyle intervention programme for patients with class III obesity

ID: 

53

DZPG Site: 

Tübingen
General Information
Status

Other

Other status

Since 2014 ongoing in the clinical setting. This program is continously used for research.

Description

Interdisciplinary 6-month lifestyle intervention programme for patients with obesity (VIADUKT). The programme targets patients with obesity, with the majority of them having Class 3 obesity (mean BMI = 42.7 kg/m2). Per year between 80 and 120 patients participate.

Paper

Attitude Matters! How Attitude towards Bariatric Surgery Influences the Effects of Behavioural Weight Loss Treatment. Bauer K, Schild S, Sauer H, Teufel M, Stengel A, Giel KE, Schellhorn P, Junne F, Nieß A, Zipfel S, Mack I. Obes Facts. 2021;14(5):531-542. doi: 10.1159/000517850; PMID: 34521092

Contact
PI

Dr. Isabelle Mack

Further PIs

Stephan Zipfel Andreas Stengel

Survey Results
Is it an interventional or non-interventional study?
  • Interventional
Specification of study type
  • Single group
Is it a mono- or multicentric study?

Monocentric

Is it a single or multi country study?

Single

Which country?

Germany

Who are participants?
  • Patients with specific diseases
Which diseases? (ICD-11 classification)
  • Mental, behavioural or neurodevelopmental disorders (06)
  • Other
Mental, behavioural or neurodevelopmental disorders (ICD-11 classification)
  • Mood disorders
  • Anxiety or fear-related disorders
  • Feeding or eating disorders
  • Disorders of bodily distress or bodily experience
  • Impulse control disorders
Recruitment setting
  • Outpatient
Target sample size

80-120 per year

Obtained sample size

450

Start of recruitment

2014

End of recruitment

ongoing

Minimum age of participants

18

Data sources for the study
  • Biological samples
  • Questionnaire
Is it planned to share the data?

No, there is no plan to make data available

Additional information about data sharing

Please contact us if this setting is interesting for future research questions.

Are further follow-ups planned?

Yes

Is there consent to re-contact participants?

Yes

Is the implementation of further study components possible?

Yes

View raw data