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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00635011
Enrollment
100
Registered
2008-03-13
Start date
2008-02-29
Completion date
2017-12-31
Last updated
2018-02-27

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

Conditions

Obesity, Morbid

Keywords

comorbidity, Quality of Life, Body Weight Changes

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.

Interventions

BEHAVIORALpsychotherapy

Cognitive Behavioral therapy

Sponsors

Helse Vest
CollaboratorOTHER
Helse Fonna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
psychiatric comorbidityfive years

Secondary

MeasureTime frame
weight lossfive years

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026