Systemic sclerosis Musculoskeletal Diseases Systemic sclerosis
Conditions
Interventions
Intervention group: 16 patients treated for 5 weeks (twice a week, 1 hour per session) with manual lymph drainage at upper limbs.
Control group: 16 patients asked to maintain their lif
Sponsors
University of Florence (Italy)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Both males and females, no age limits 2. Systemic sclerosis patients with oedematous hands fulfilling the American College of Rheumatology (ACR) criteria
Exclusion criteria
Exclusion criteria: 1. Patients that do not meet the inclusion criteria 2. Ongoing infections and thrombosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The following items assessed at baseline, at the end of treatment (after 5 weeks) and after 9 weeks of follow-up. 1. Hands volume assessed by volumetric test 2. Hands function evaluated by Hand Mobility in Scleroderma (HAMIS) test, assessed in both hands | — |
Secondary
| Measure | Time frame |
|---|---|
| The following items assessed at baseline, at the end of treatment (after 5 weeks) and after 9 weeks of follow-up: 1. 4 visual assessment scales (VAS) 0-10 (0= best condition;10= worst condition) by which the patient self-assesses the entity (in the previous week) of 1.1. Hand oedema 1.2. Hand pain 1.3. The interference of hand oedema on the daily activities 1.4. The inferference of hand pain on the daily activities. 2. Quality of life, assessed by the 36-item Short Form (SF-36) Health Survey and Health Assessment Questionnaire (HAQ) | — |
Countries
Italy
Outcome results
None listed