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Thoracic Paraspinal Soft Tissue Mobilizations in Treatment of Patients With Upper Limb Complex Regional Pain Syndrome

Not Applicable
Completed
Conditions
Complex Regional Pain Syndromes
Interventions
Diagnostic Test: massage
Registration Number
NCT03111225
Lead Sponsor
Reuth Rehabilitation Hospital
Brief Summary

This study examines the prevalence of trigger points in muscles in the thorax in upper limb Complex Regional Pain Syndrome (CRPS) patients, compared to healthy subjects. In addition, we will examine if adding treatment to muscles in the thoracic area (to the regular physical therapy treatment) will alleviate some of the sensitivity in the upper limb in CRPS patients.

Detailed Description

This study examines the prevalence of trigger points in muscles in the thorax in upper limb Complex Regional Pain Syndrome (CRPS) patients, compared to healthy subjects. The muscles that will be examined are: Subclavius, Pectoralis minor, Rhomboids, Infraspinatus and Serratus superior posterior.

In addition, we will examine if adding treatment to muscles in the thoracic area (to the regular physical therapy treatment) will alleviate some of the sensitivity in the upper limb in CRPS patients.This will be examined in an A-B-A design: at first the patients will be examined. Then they will recieve conventional physiotherapy treatment for a month. After a month, they will be examined again, and then they will recieve soft tissue massage to the thoracic area for 15 minutes in addition to the conventional physiotherapy treatment. After a month of the combined treatment, the patients will be examined a third and final time.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CRPS patientsmassageCRPS patients that will be examined for trigger points in the thoracic muscles. 10 out of the 23 will also be included in the intervention stage and will recieve a month of conventional physiotherapy, and a month of conventional physiotherapy with addition of massage to the thoracic area.
Primary Outcome Measures
NameTimeMethod
Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire10 minutes

Questionnaire that examines upper limb function

Secondary Outcome Measures
NameTimeMethod
skin rolling test1 minute
Pressure algometer10 minutes

pressure pain threshold

Goniometer1 minute

shoulder flexion range of motion

CRPS severity score (CSS)20 minutes

form filled by an MD after an interview and examination of a patient

Allodynia in scapula, arm and forearm5 minutes

von Frey filaments

trigger point examination5 minutes
NPRS1 minute

Numerical Pain Rating Scale

Trial Locations

Locations (1)

Reuth Rehabilitation Hospital

🇮🇱

Tel Aviv, Israel

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