A Preoperative Cognitive Behavioural Therapy Program Based on Self-determination Theory for Bariatric Surgery Candidates

Obesity Clinical Trial

— ACRoBAT  

Official title:

Evaluation of a Preoperative Cognitive Behavioural Therapy (CBT) Program Based on Self-determination Theory for Bariatric Surgery Candidates : an Open-label Controlled, Randomized, Superiority Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03976674
• Other study ID #: RC-P0061
• Status: Completed
• Phase: N/A
• Start date: February 5, 2018
• Est. completion date: September 10, 2020

Study information

• Verified date: February 2024
• Source: Lille Catholic University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to evaluate the impact of a pre-surgical intervention program based on Cognitive and Behavioural Emotional Therapies, on the degree of dietary restriction of patients who are candidates for bariatric surgery in order to increase the long-term effectiveness of this kind of surgery

Recruitment information / eligibility

• Status: Completed
• Enrollment: 94
• Est. completion date: September 10, 2020
• Est. primary completion date: September 5, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Patient starting a preparation for bariatric surgery in the endocrinology department at St Philibert Hospital

• 18 =Age=60 years

• Patient meeting the criteria of the High Authority of Health (HAS) for the agreement of a bariatric treatment

• Patient affiliated to the social security

• Patient giving informed consent

Exclusion Criteria:

• Low level of comprehension of French

• Pregnant women

• Patient under guardianship or curatorship.

Related Conditions & MeSH terms

• Bariatric Surgery Candidate
• Obesity

Intervention

Behavioral:
• Cognitive Behavioural Therapy (CBT)
5 group sessions (2h30/session) before the surgery

Locations

Country	Name	City	State
France	• Lille Catholic University Hospital Group, Saint Philibert Hospital	Lomme	Haits De France

Sponsors (1)

Lead Sponsor	Collaborator
Lille Catholic University

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Eating Disorder Examination-Questionnaire (EDE-Q) score	The EDE-Q is a 28 item self-report questionnaire. It concerns behaviors over a 28-day time period and retains the scoring system of 0-6: 0 = behaviour was absent and 6 = behaviour was present daily or to an extreme degree	One year after therapy