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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02431195
Other study ID # 13SCW-SOCIOB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2015
Est. completion date June 2019

Study information

Verified date June 2019
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this study is to identify changes in eating behaviors and physical activity in patients after bariatric surgery and their family members living in same household: children aged between 11-17 years, spouse, parents, cohabitee or partner in a civil union.


Description:

As secondary objectives, the study aims to:

- Describe the sociodemographic and clinical characteristics of post bariatric surgery patients.

- Assess changes in quality of life of the post-surgery patients.

- Explain changes of post-surgery in eating behavior and activity varied according to gender

- Explain changes of post-surgery in eating behavior and activity varied according to socio-economic conditions

- Explain changes of post-surgery in eating behavior and activity varied according to inter-generational relation

- Have a overview on the surgery as a turning point in the life of patients

- Estimate the relevant message of cares given to patients, in order to better adjust medical intervention, in conjunction with patients and their family members.

This is a prospective observational study. It will be performed in two university hospitals: CHU Ambroise Paré at Boulogne-Billancourt city and CHU Pitié Salpétrière at Paris, in nutrition department and metabolic surgery department. The study will involve collaboration of a team of social researchers.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date June 2019
Est. primary completion date February 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Aged = 18 years

- Eligible to undergo bariatric surgery

- Post bariatric surgery follow-up visits will take place in the nutrition department

- Living together with family member (children aged 11-17 years, parents, spouse, cohabitee or partner in civil union)

- Informed consent signed

Exclusion Criteria:

- Higher-order cognitive disorders

- Language difficulties in understanding

- Living alone or living without any family member

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Department of Nutrition, CHU Ambroise Paré Boulogne Billancourt Hauts Des Seine

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes from baseline in different eating habits and culinary items in responses to questionnaires Changes from baseline in different eating habits and culinary items in responses to questionnaires at 3 months, 6 months and 1 year after bariatric surgery. It is expected that patient's feeding practice should be in accordance with the postsurgical dietary guidelines. At 3 month, 6 month and 12 month
Secondary Changes from baseline in different items about physical activity in responses to questionnaires Changes from baseline in different items about physical activity in responses to questionnaires at 3 months, 6 months and 1 year after bariatric surgery. It is expected that patient's physical activity practice should be in accordance with the postsurgical guidelines. At 3 month, 6 month and 12 month
Secondary Quality of life measured by scores Quality of life will be measured by scores at baseline, 3 month, 6 month and 12 month At baseline, 3 month, 6 month and 12 month
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