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Clinical Trials/NCT03319264
NCT03319264
Completed
Not Applicable

Sarcopenia in Axial and Peripheral Spondyloarthropathies

Hospices Civils de Lyon1 site in 1 country106 target enrollmentNovember 2, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spondylarthropathy
Sponsor
Hospices Civils de Lyon
Enrollment
106
Locations
1
Primary Endpoint
Walking speed
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

Spondylarthropathies (SpA) are among the most common chronic inflammatory rheumatisms in adults, responsible for a muscular loss or sarcopenia which can be very disabling, not much documented in the literature, and not yet studied in France. In addition, sarcopenia is associated with decreased physical activity and increased risk of falls and fractures. A better characterization of the determinants of this muscular loss will allow to better detect and take care of it.

The aim is to conduct the first French study on the prevalence and severity of sarcopenia in patients with spondyloarthropathies and to study the variables that may be associated with it. Finally, we propose to evaluate obesity related to sarcopenia in these patients and compare them to cases matched for age and sex (from OFELY / STRAMBO cohorts, Lyon, FRANCE).

This is a prospective interventional and monocentric study with minimal risks and constraints: patients will be included for one day for an evaluation of their sarcopenia by measuring their muscle strength, physical performance and body composition and recording of their socio-demographic and disease characteristics.

Registry
clinicaltrials.gov
Start Date
November 2, 2017
End Date
July 4, 2018
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men and women, 18 to 80 years old
  • Hospitalized or attending the rheumatology department for spondyloarthopathy.

Exclusion Criteria

  • no signed consent
  • Immobilization for a period of more than 15 days during the last 3 months
  • pregnant or breastfeeding woman
  • Not affiliated to the national healthcare insurance
  • difficulty in understanding French
  • psychiatric disorder

Outcomes

Primary Outcomes

Walking speed

Time Frame: At day 1

Walking speed is a physical performance outcome, that is the second outcome to evaluate sarcopenia

Muscular mass

Time Frame: Up to 4 month after inclusion

Muscular mass is the third outcome to evaluate sarcopenia and will be assessed using DXA

Muscular strength

Time Frame: At day 1

Muscular strength is the first outcome to evaluate sarcopenia

Secondary Outcomes

  • Alcohol consumption(At day 1)
  • Time of sport practice per month(At day 1)
  • Physical activity rate in work(At day 1)
  • Average walking time in a week(At day 1)
  • Tobacco consumption(At day 1)
  • Score at the SARQOL questionnaire(At day 1)

Study Sites (1)

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