MedPath

Pre- and Postoperative Cognitive Behavior Therapy for Patients Accepted for Bariatric Surgery

Not Applicable
Completed
Conditions
Obesity, Morbid
Registration Number
NCT00635011
Lead Sponsor
Helse Fonna
Brief Summary

The purpose of this study is to investigate the relationship between the potential predictive psychological variables and success after bariatric surgery. The investigators will also investigate the purpose of a pre- and postoperative psychological intervention.

Detailed Description

Bariatric surgery is the treatment of choice for morbid obesity, but it does not lead to equal results in every patients. Research about personality factors involved in successful outcome after bariatric surgery has led to contrasting results. The existing literature about potential predictors of success after bariatric surgery is far from conclusive. The investigators want to evaluate preoperatively by standardized diagnostic interviews (MINI, SCID-II) and rating scales and questionnaires to assess co-morbid psychopathology. The same evaluation will be done after 1,2 and 5 years. The investigators will look for a relationship between psychological variables and success after bariatric surgery, including amount of weight loss, psychiatric comorbidity, quality of life and employment. The investigators will also investigate the purpose of an pre- and postoperative psychological intervention. Patients on a waiting list for bariatric surgery are randomised to an intervention- and a control group. The intervention is based on cognitive behavior therapy and mindfulness, 6 weeks preoperative and two weeks postoperative programme. Outcome measures are amount of weight loss, psychiatric comorbidity, quality of life and employment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Patients on a waiting list for bariatric surgery at Haugesund hospital
Exclusion Criteria
  • Patients with psychosis and suicidality
  • Suicidal attempts the last two years
  • Or suicidal thoughts or plans.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
psychiatric comorbidityfive years
Secondary Outcome Measures
NameTimeMethod
weight lossfive years

Trial Locations

Locations (1)

Haugesund Hospital, Helse Fonna HF

🇳🇴

Haugesund, Rogaland, Norway

© Copyright 2025. All Rights Reserved by MedPath