Psychological Impact of Quarantine in Chronic Pain Patient During COVID-19 Outbreak
DolPsyCOVID
2 other identifiers
observational
312
1 country
1
Brief Summary
In the context of quarantine with COVID-19, we will study the experience and psychological impact of pain in adult patients living with chronic pain. We will evaluate the link between the question of physical and psychological confinement in the experience of pain in this particular situation
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 15, 2020
CompletedFirst Posted
Study publicly available on registry
April 20, 2020
CompletedStudy Start
First participant enrolled
April 20, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 27, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
April 27, 2020
CompletedDecember 11, 2020
May 1, 2020
7 days
April 15, 2020
December 10, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Hospital Anxiety and Depression Scale questionnaire
1 week from baseline on
Secondary Outcomes (3)
Quality of life (SF36)
1 week from baseline on
self-reported questionnaire for painful
1 week from baseline on
qualitive questionnaire
1 week from baseline on
Study Arms (1)
patient with chronic painful
Interventions
Eligibility Criteria
RA patient will be interviewed par internet questionnaire (patient association / AFVD)
You may qualify if:
- Patient with chronic pain
- Patient in confinement
- Patient with sufficient understanding of the French language
You may not qualify if:
- Non adult patient
- patient without quarantine
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hopital Roger Salengro, CHU Lille
Lille, 59037, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anne BERA, MD
University Hospital, Lille
Study Design
- Study Type
- observational
- Observational Model
- FAMILY BASED
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 15, 2020
First Posted
April 20, 2020
Study Start
April 20, 2020
Primary Completion
April 27, 2020
Study Completion
April 27, 2020
Last Updated
December 11, 2020
Record last verified: 2020-05