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NCT04621084 Clinical Trial

Influence of the COVId-19 Pandemic on STRESS and Eating Habits

Nutrition Clinical Trial

— COVISTRESSNutr  

Official title:
Influence of the COVId-19 Pandemic on STRESS and Eating Habits

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04621084
Other study ID # 2020 COVISTRESS NUTRITION
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2020
Est. completion date December 31, 2025

Study information
Verified date November 2020
Source University Hospital, Clermont-Ferrand
Contact Lise Laclautre
Phone 0473754963
Email promo_interne_drci@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Coronavirus has caused containment of more than a third of the world's population. Containment can drastically change lifestyle habits, including eating habits such as the number of meals, meal times or their composition. However, there is currently no data on the influence of confinement on eating habits.

Description:

This is an observational study by REDCap questionnaire® via a flyer deposited in the waiting room of the COVID screening centres. No incentive to complete the questionnaire will be made. The self-administered questionnaire will assess stress, changes in eating habits, and relationships with socio-demographic or lifestyle factors. This questionnaire includes 9 specific questions on nutrition and 40 general questions.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years and older
Eligibility Inclusion Criteria: - All volunteers who are screened Exclusion Criteria: - none

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Eating habits
Questionnary online

Locations
Country Name City State
France Clermont-Ferrand University Hospital clermont-Ferrand Aura

Sponsors (2)
Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand Faculty of Medicine and Paramedical Professions, Clermont-Ferrand, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Other Sociodemographic characteristics Age, gender, qualification, personal work status, ethnicity, life characteristics and stress will be assessed by questionnaires Day 1
Primary Stress measures Attitudes and stress related to screening procedure will be measured via questionnaire Day 1
Secondary Nutrition Eating habits will be measured via questionnaire Day 1
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