Spondylarthritis Clinical Trial
NCT number | NCT03999489 |
Other study ID # | LOCAL/2013/CGV-01 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 2015 |
Est. completion date | June 2015 |
Verified date | June 2019 |
Source | Centre Hospitalier Universitaire de Nimes |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The general main objective of our study is to investigate the psychometric properties, the
levels and determinants of the extent of SF- 6D utility in patients followed for recent back
pain inflammatory disease.
The specific objectives are :
- Study the feasibility of the tool considering missing data, distribution, construct
validity, reproducibility, sensitivity to change or clinically different groups
(discriminative ability) the extent of SF -6D utility .
- Study the impact of socio-demographic characteristics, disease characteristics and
quality of life, comorbidities at baseline on the measurement of utility and sensitivity
to change.
Status | Completed |
Enrollment | 708 |
Est. completion date | June 2015 |
Est. primary completion date | June 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - The patient should be given free and informed consent and signed the consent - The patient must be affiliated or beneficiary of a health insurance plan - patients aged 18 years and under 50 - inflammatory back pain (buttocks , lumbar or thoracic spine ) - fulfilling the criteria of Calin or Berlin (30,31) - duration of symptoms than three months and less than three years - symptoms suggestive of spondyloarthritis as assessed by the local investigator ( score=5 on a numerical scale from 0 to 10 where 0 = no evocative and 10 = very suggestive of spondyloarthritis ) . Exclusion Criteria: - Another clearly defined spinal disease (eg discarthrose ) - history of treatment with biotherapy - taking glucocorticoids allowed only in low dose of less than 10mg of prednisone daily and stable for at least four weeks before inclusion - Current or history anomalies that could interfere with the validity of informed consent and / or prevent a patient's optimal adhesion to the cohort (eg , alcoholism , mental illness) . |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Nimes |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Level of utility measured by the SF-6D | The SF-6D derives from 11 questions of the SF36 using the algorithm of Brazier et al which then provides a unique score. It has 6 dimensions: Physical Function, Role Limitation, Social Function, Pain, Mental Health and Vitality with 4 to 6 levels of responses depending on the dimension. SF-6D thus makes it possible to describe 18,000 health conditions. The utility score obtained with SF-6D varies between 0.29 and 1. | baseline (0 months) | |
Primary | Level of utility measured by the SF-6D | The SF-6D derives from 11 questions of the SF36 using the algorithm of Brazier et al which then provides a unique score. It has 6 dimensions: Physical Function, Role Limitation, Social Function, Pain, Mental Health and Vitality with 4 to 6 levels of responses depending on the dimension. SF-6D thus makes it possible to describe 18,000 health conditions. The utility score obtained with SF-6D varies between 0.29 and 1. | 6 months | |
Primary | Level of utility measured by the SF-6D | The SF-6D derives from 11 questions of the SF36 using the algorithm of Brazier et al which then provides a unique score. It has 6 dimensions: Physical Function, Role Limitation, Social Function, Pain, Mental Health and Vitality with 4 to 6 levels of responses depending on the dimension. SF-6D thus makes it possible to describe 18,000 health conditions. The utility score obtained with SF-6D varies between 0.29 and 1. | 12 months |
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