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NCT04353011 Clinical Trial

Psychological Impact of Quarantine in Chronic Pain Patient During COVID-19 Outbreak

Chronic Pain Clinical Trial

— DolPsyCOVID  

Official title:
Psychological Impact of Quarantine in Chronic Pain Patient During COVID-19 Outbreak

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04353011
Other study ID # 2020_45
Secondary ID 2020-A00912-37
Status Completed
Phase
First received
Last updated
Start date April 20, 2020
Est. completion date April 27, 2020

Study information
Verified date May 2020
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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

Recruitment information / eligibility
Status Completed
Enrollment 312
Est. completion date April 27, 2020
Est. primary completion date April 27, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with chronic pain - Patient in confinement - Patient with sufficient understanding of the French language Exclusion Criteria: - Non adult patient - patient without quarantine

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire assesment
questionnaire assesment

Locations
Country Name City State
France Hopital Roger Salengro, CHU Lille Lille

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hospital Anxiety and Depression Scale questionnaire 1 week from baseline on
Secondary Quality of life (SF36) 1 week from baseline on
Secondary self-reported questionnaire for painful 1 week from baseline on
Secondary qualitive questionnaire 1 week from baseline on
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