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Sarcopenia in Axial and Peripheral Spondyloarthropathies

Sarcopenia in Axial and Peripheral Spondyloarthropathies

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03319264
Acronym
SASPAR
Enrollment
106
Registered
2017-10-24
Start date
2017-11-02
Completion date
2018-07-04
Last updated
2025-12-19

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

Conditions

Spondylarthropathy, Sarcopenia

Keywords

Spondylarthropathy, Sarcopenia, lean mass, fat mass

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.

Interventions

OTHERDynamometry exam

Prehension strength of the main hand will be assessed thanks to dynamometry, in order to evaluate patient's muscular strength

A 4 metres walking test will be performed to assess patient's walking speed

RADIATIONDXA measurement

DXA measurement will be performed to assess patient's body composition

OTHERSARQOL questionnaire

Patient's quality of life will be assessed thanks to the SARQOL questionnaire

BEHAVIORALLife habits Questionnaire

Life habits Questionnaire

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Muscular strengthAt day 1Muscular strength is the first outcome to evaluate sarcopenia
Walking speedAt day 1Walking speed is a physical performance outcome, that is the second outcome to evaluate sarcopenia
Muscular massUp to 4 month after inclusionMuscular mass is the third outcome to evaluate sarcopenia and will be assessed using DXA

Secondary

MeasureTime frameDescription
Physical activity rate in workAt day 1Physical activity rate in work can be light, medium, high or not applicable if the patient does not work ; it is the second outcome to evaluate patient's physical global activity.
Alcohol consumptionAt day 1
Score at the SARQOL questionnaireAt day 1Quality of life will be assessed thanks to the SARQOL questionnaire (score between 0 and 100)
Average walking time in a weekAt day 1Average walking time in a week is the third outcome to evaluate patient's physical global activity.
Tobacco consumptionAt day 1
Time of sport practice per monthAt day 1Number of hours of sport practice per month is the first outcome to evaluate patient's global physical activity.

Countries

France

Outcome results

None listed

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