Psychological Impact of Quarantine in Rheumatoid Arthritis Patient During COVID-19 Outbreak (PRPsyCOVID)
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|ClinicalTrials.gov Identifier: NCT04351399|
Recruitment Status : Completed
First Posted : April 17, 2020
Last Update Posted : May 21, 2020
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.
|Condition or disease||Intervention/treatment|
|Sars-CoV2 Rheumatic Diseases Rheumatoid Arthritis Chronic Pain||Other: questionnaire assesment|
|Study Type :||Observational|
|Actual Enrollment :||318 participants|
|Official Title:||Psychological Impact of Quarantine in Rheumatoid Arthritis Patient During COVID-19 Outbreak|
|Actual Study Start Date :||April 27, 2020|
|Actual Primary Completion Date :||May 4, 2020|
|Actual Study Completion Date :||May 4, 2020|
|patient with chronic painful inflammatory rheumatism||
Other: questionnaire assesment
The questionnaire will ask questions around their socio-demographic characteristics,quality of life, painful, using analgesic , since they are in quarantine
- Frequency of RA patients with emotional impact (feeling of isolation) [ Time Frame: maximum 1 week from baseline on ]
- self-reported questionnaire for painful [ Time Frame: maximum 1 week from baseline on ]Self reported questionnaire with questions to assess the characteristic,intensity of pain on quality of life, and consumption of analgesic.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04351399
|Hopital Roger Salengro, CHU Lille|
|Lille, France, 59037|
|Principal Investigator:||René-Marc FLIPO, MD,PhD||University Hospital, Lille|