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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04351399
Other study ID # 2020_29
Secondary ID 2020-A00907-32
Status Completed
Phase
First received
Last updated
Start date April 27, 2020
Est. completion date May 4, 2020

Study information

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

Clinical Trial Summary

Clinical data about psychological impact of quarantine are well studied in transient event or more prolonged situation like jail incarceration. In recent metaanalysis, psychological impact of quarantine was well documented in a specific population during first SARS epidemy. Even after the end of quarantine several patients were still with symptom of avoiding mainly agoraphobia, frequent hand washing and a carefull return to normal life COVID-19 infection is already associated with psychological symptom like anxiety, depression, sleep disorders and symptoms of acute stress However psychological impact of quarantine is on none in chronic painful inflammatory rheumatism in France. The prevalence of rheumatoid arthritis is 0.5% of the population with frequent comorbidity such as anxiety and depression. During the quarantine secondary to COVID-19 pandemic it's possible to evaluated the psychological impact of adult RA patients. The present study is an "emergency" being realize before the end of the quarantine.


Recruitment information / eligibility

Status Completed
Enrollment 318
Est. completion date May 4, 2020
Est. primary completion date May 4, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Rheumatoid arthritis Quarantine Exclusion Criteria: - Non adult patient RA patient without quarantine

Study Design


Intervention

Other:
questionnaire assesment
The questionnaire will ask questions around their socio-demographic characteristics,quality of life, painful, using analgesic , since they are in quarantine

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 Frequency of RA patients with emotional impact (feeling of isolation) maximum 1 week from baseline on
Secondary self-reported questionnaire for painful Self reported questionnaire with questions to assess the characteristic,intensity of pain on quality of life, and consumption of analgesic. maximum 1 week from baseline on
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