MAVIPAN: My Life and the COVID-19 Pandemic

NCT04575571 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2020-10-05

No results posted yet for this study

Summary

The health crisis imposed by COVID-19 is forcing major worldwide social reorganization that will have profound consequences on our society. Currently, one-third of the world's population (\~3 billion individuals) is living under some kind of isolation or quarantine measures, causing an unprecedented and rapidly evolving psychosocial crisis.

The psychosocial consequences of this health crisis will persist long after restriction measures are lifted and the pandemic is over. This impact will be significant for individuals facing unique contexts or challenges (e.g., older adults, individuals living with a disability, underprivileged families) and will most likely exacerbate existing social and gender inequalities in health and human development.

There is an urgent need for information on the evolution of the psychosocial dimensions of health and coping strategies used by our population and our health and social services structures. Thus, this study is designed to accelerate the availability of high-quality, real-time evidence within health and social services structures to address, support and minimize psychosocial consequences of the COVID-19 pandemic. Through constantly evolving research questions responsive to the course of the pandemic evolution, the rapid system transformations and adaptation of services, and knowledge users (KUs) needs, MAVIPAN aims to address, document, monitor, and evaluate the following:

1. Individuals and families' adjustments and mitigation strategies, especially for those considered vulnerable and in high-risk contexts.
2. Healthcare and social services workers and managers' adjustments and mitigation strategies.
3. The organization of service structures.
4. The social and economic response.

To achieve these objectives, we use a mixed methods study design that combines quantitative questionnaires and qualitative interviews to deepen our understanding of elements such as the coping strategies used during the pandemic. A first measure was taken during lock-down as well as a follow-up at 3 months. Another follow-up will be made at 7 months. At least one per year follow-up will be made over the course of the study (5 years). Additional measures may be taken depending on the evolution of the pandemic and the sanitary measures put in place by the authorities.

Conditions

  • Psychosocial Impacts of the COVID-19 Pandemic

Interventions

OTHER

No intervention, this is an observational study that uses validated questionnaires and qualitative interviews..

No intervention, this is an observational study that uses validated questionnaires and qualitative interviews.

Sponsors & Collaborators

  • VITAM: Research Center on Sustainable Health

    collaborator UNKNOWN
  • Centre de recherche CERVO

    collaborator UNKNOWN
  • Centre Interdisciplinaire de Recherche en Réadaptation et Intégration Sociale

    collaborator OTHER
  • Centre de recherche universitaire sur les jeunes et les familles

    collaborator UNKNOWN
  • Réseau québécois de recherche sur le vieillissement

    collaborator UNKNOWN
  • Participation sociale et villes inclusives

    collaborator UNKNOWN
  • Société inclusive

    collaborator UNKNOWN
  • CISSS de Chaudière-Appalaches

    collaborator OTHER_GOV
  • Centre intégré de santé et de services sociaux de la Côte-Nord

    collaborator UNKNOWN
  • Fondation Mirella et Lino Saputo

    collaborator UNKNOWN
  • Ville de Québec

    collaborator UNKNOWN
  • Living Lab de Charlevoix

    collaborator UNKNOWN
  • Centre intégré de santé et de services sociaux du Bas St-Laurent

    collaborator UNKNOWN
  • Réseau provincial de recherche en adaptation réadaptation

    collaborator UNKNOWN
  • Réseau international sur le Processus de production du handicap

    collaborator UNKNOWN
  • Centre de recherche intégrée pour un système apprenant en santé et services sociaux

    collaborator UNKNOWN
  • Regroupement des organismes de personnes handicapées de la région 03

    collaborator UNKNOWN
  • Laval University

    lead OTHER

Principal Investigators

  • Annie LeBlanc, PhD · Faculty of Medecine, Laval University

Eligibility

Min Age
14 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-04-29
Primary Completion
2025-04-29
Completion
2025-04-29

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04575571 on ClinicalTrials.gov