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Social and Psychological Impacts of SARS-Cov-2 Pandemic Period in the Obese Population. (OBIMPACOV)

U

University Hospital of Bordeaux

Status

Completed

Conditions

Covid19
Obesity

Treatments

Other: Questionnaire
Other: Interview

Study type

Observational

Funder types

Other

Identifiers

NCT04910607
CHUBX 2020/38

Details and patient eligibility

About

The population suffering from obesity is particularly at risk during this pandemic period. The Nouvelle Aquitaine region is not spared, since according to the regional epidemiological report of 7 May 2020, carried out by Santé Publique France, 39.2% of cases admitted to the intensive care unit in Nouvelle Aquitaine and presenting risk factors are overweight or obese.

Other risk factors, such as social-environmental factors, must be taken into consideration. Socio-demographic surveys in this area highlight the socio-economic and territorial inequalities that interfere with obesity issues. Similarly, the issues of stigmatisation and isolation seem to be at the heart of the question of how to deal with these people.

Full description

This is a prospective multicentre study. Participating patients will be recruited from the Specialised Obesity Centres (CHU and SSR, as well as patient associations) to fill in a questionnaire and take part in an interview (a varied panel representative of the target population in terms of place of residence, socio-professional category, sex and age).

The medical and paramedical staff involved in the partner CSOs and the patients' resources (identified by the patients' associations) will also be asked to participate in a semi-directive interview.

Enrollment

279 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients 18 years of age.
  • Be registered in an active file of the 3 partner CSOs.

Exclusion criteria

  • Patients under 18 years of age.

  • Patients under protective measures or deprived of liberty:

    • pregnant or breastfeeding woman,
    • under guardianship,
    • under guardianship,
    • safeguard of justice,
    • incarcerated.

Trial design

279 participants in 2 patient groups

Patient
Description:
Participating patients will be recruited from the Specialised Obesity Centres =CSO (CHU and Follow-up and rehabilitation care (SSR), as well as patient associations) to fill in a questionnaire and take part in an interview (varied panel representative of the target population in terms of place of residence, socio-professional category, sex and age).
Treatment:
Other: Questionnaire
Other: Interview
Professional
Description:
Medical and paramedical staff involved in the partner CSOs will also be asked to participate in a semi-structured interview.
Treatment:
Other: Interview

Trial contacts and locations

3

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Central trial contact

Maud MONSAINGEON-HENRY, Dr; Blandine GATTA-CHERIFI, Pr

Data sourced from clinicaltrials.gov

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