Skip to main content
Clinical Trials/NCT00635011
NCT00635011
Completed
N/A

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

Helse Fonna1 site in 1 country100 target enrollmentFebruary 2008
ConditionsObesity, Morbid

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obesity, Morbid
Sponsor
Helse Fonna
Enrollment
100
Locations
1
Primary Endpoint
psychiatric comorbidity
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
December 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Helse Fonna
Responsible Party
Principal Investigator
Principal Investigator

Haldis Økland Lier

PhD, medical doctor

Helse Fonna

Eligibility Criteria

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.

Outcomes

Primary Outcomes

psychiatric comorbidity

Time Frame: five years

Secondary Outcomes

  • weight loss(five years)

Study Sites (1)

Loading locations...

Similar Trials