Impact of the COVID-19 pandemic on stress and eating habits
Influence of the COVId-19 Pandemic on STRESS and Eating Habits
This study looks at how the COVID-19 pandemic has changed people's stress levels and eating habits by asking them questions about their nutrition and lifestyle.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 10 Years and up |
| Sex | All |
| Sponsor | University Hospital, Clermont-Ferrand Academic / other |
| Locations | 1 site (clermont-Ferrand, Aura) |
| Trial ID | NCT04621084 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess how the COVID-19 pandemic has influenced stress levels and eating habits among individuals. Participants will complete a self-administered questionnaire that includes specific questions about nutrition and general questions related to their lifestyle and socio-demographic factors. The study will gather data through flyers placed in COVID screening centers, allowing for a broad collection of responses without any incentives for participation. The findings will help understand the relationship between confinement and changes in eating behaviors.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals who have been screened at COVID-19 screening centers and are willing to share their experiences regarding stress and eating habits.
Not a fit: Patients who are not affected by the COVID-19 pandemic or those who do not experience changes in their eating habits may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into how the pandemic has affected nutrition and stress, potentially guiding public health interventions.
How similar studies have performed: While there may be limited data on this specific topic, other studies have explored the impact of pandemics on lifestyle changes, suggesting that this area of research is relevant and necessary.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All volunteers who are screened Exclusion Criteria: * none
Where this trial is running
clermont-Ferrand, Aura
- Clermont-Ferrand University Hospital — clermont-Ferrand, Aura, France (Recruiting)
Study contacts
- Study coordinator: Lise Laclautre
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 0473754963
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.