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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03306784
Other study ID # RC17_0182
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 3, 2017
Est. completion date January 31, 2018

Study information

Verified date September 2021
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fulfilling by all patients consequently seen by 6 rheumatologists in a same outpatient rheumatology clinic (in at least one month period) of a set of 6 questionnaires, including RAPID3 and pain catastrophizing scales.


Description:

Fulfilling by all patients (seen by 6 rheumatologists in a same outpatient rheumatology clinic from a university French hospital in at least one month period) of a set of 6 questionnaires including a RAPID3 score (Routine Assessment of Patient Index Data 3) and pain catastrophizing scale, as well as Pain detect and Hospital Anxiety and Depression scale questionnaires (HAD) , in ten predefined categories of disorders: rheumatoid arthritis; any spondyloarthritis; other inflammatory rheumatisms or systemic disorders; osteoarthritis of the upper part of the body; osteoarthritis of the lower part of the body; back pain and/or radiculalgia; bone disorders, including osteoporosis; tendinosis and other soft tissue conditions; peripheral neuropathy, including entrapment neuropathies; fibromyalgia and related conditions.


Recruitment information / eligibility

Status Completed
Enrollment 572
Est. completion date January 31, 2018
Est. primary completion date January 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - any outpatient aged 18 or more, agreeing to fulfil the set of 6 questionnaires - Man or woman coming to the Rheumatology Department of the Nantes University Hospital with a senior rheumatologist Exclusion Criteria: - Patients not fluent enough in French or suffering from neurological or psychological disorders making their responses unreliable

Study Design


Intervention

Other:
questionnaires
questionnaires, including RAPID3 and pain catastrophizing scales

Locations

Country Name City State
France CHU de Nantes Nantes

Sponsors (1)

Lead Sponsor Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ranking of PCS scores according to the underlying disorders (10 predefined categories), and also ranking of RAPID-3 scores according to the underlying disorders (10 predefined categories). Composite score: RAPID3 (0-30) and PCS (0-52) are widely used scales, suitable for routine fulfillment by outpatients. At least one month for each physician, and at least 30 patients in each category (whatever the physician seen).
Secondary Ranking of correlations between RAPID3 and Pain catastrophizing scale (PCS) (13 items) scores in the 10 subsets of categories listed above (from the strongest correlation to the lowest correlation) RAPID3 (0-30) and PCS (0-52) are widely used scales, suitable for routine fulfillment by outpatients At least one month for each physician, and at least 30 patients in each category (whatever the physician seen).
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