Skip to main content
OpenTrials
Completed

NCT Number: NCT00635011

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Haugesund Hospital, Helse Fonna HF

Haugesund, Rogaland, N-5504, Norway

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Psychotherapy

Behavioral

Cognitive Behavioral therapy

Primary outcomes

  1. psychiatric comorbidity

    Time frame: five years

Secondary outcomes

  1. weight loss

    Time frame: five years

Sponsors and collaborators

Lead sponsor

Helse Fonna

Other

Collaborators

  • Helse Vest

Registry information

Important dates

Study start
2008
Primary completion
2011
Study completion
2017
First posted
Mar 13, 2008
Registry last updated
Feb 27, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.