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Virtual Management of Rheumatoid Arthritis

Evaluation of Rheumatoid Arthritis at the Time of Telemedicine

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05124782
Acronym
ePRAT
Enrollment
70
Registered
2021-11-18
Start date
2021-11-30
Completion date
2023-11-22
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Keywords

Rheumatoid arthritis, Virtual consultation, Telemedicine, Patient reported outcome

Brief summary

The purpose of this study is to optimize the care of patients with RA seen in virtual consultation.

Detailed description

This study will be organized in two consecutive steps: 1. A first descriptive step that will consist of a retrospective analysis of virtual consultation records of patients with RA during the pandemic and lockdown period in order to analyze on which criteria the patients were assessed and followed during this period. 2. The second step will consist in evaluating the interest of the systematic use in virtual consultation of a patient reported outcome (PRO), the RAID (Rheumatoid Arthritis Impact of Disease) questionnaire; and analyze how its results influence the rheumatologist decision-making.

Interventions

OTHERRheumatoid Arthritis Impact of Disease questionnaire

Rheumatoid Arthritis Impact of Disease questionnaire

Sponsors

URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients with rheumatoid arthritis fulfilling the 2010 ACR/EULAR classification criteria * Follow-up in the rheumatology department of Cochin Hospital * Affiliated with a social security scheme * Non-opposition to participating in the study * Patients with a valid email address (registration to the virtual consultation system)

Exclusion criteria

* Opposition to participate to this research * Inability to understand or speak French * Patient under tutor or curator ship * patients under medical state help

Design outcomes

Primary

MeasureTime frameDescription
Rate of face to face consultation, hospitalization and therapeutic modificationsInclusionThe primary outcome will be the rate of face to face consultation, hospitalization and therapeutic modifications decided by the rheumatologist during the virtual consultation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026