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The effect of a wrist orthosis night using in the pain and paresthesia in persons with carpal tunnel syndrome

Randomized clinical trial of nocturnal wrist orthosis therapy in the function and symptoms of carpal tunnel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-74rqnz
Enrollment
Unknown
Registered
2016-03-15
Start date
2014-06-04
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Carpal Tunnel Syndrome

Interventions

Experimental group 1: twelve subjects with carpal tunnel syndrome and use of a commercial wrist orthosis plus exercises performed at home. Experimental group 2: twelve subjects with carpal tunnel synd
Other
E02.760.169.063.500.387

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
Universidade Federal de São Paulo
Collaborator

Eligibility

Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Medical and kinetic-functional diagnosis of carpal tunnel syndrome; test electromyography to report to carpal tunnel syndrome in grade I or II; absence of musculoskeletal disorders in elbow and shoulder joints; pain and symptoms present for at least six months; active range of motion of shoulder flexion and abduction greater than or equal 120°; active range of motion of elbow flexion of 100° and wrist extension of 30°; positivity for Tinel and Phalen tests.

Exclusion criteria

Exclusion criteria: History of trauma or previous surgery in the upper extremities or spine; subluxation of acromioclavicular joint and/or glenohumeral joint; osteoarthritis or tendinopathy in the shoulder, elbow, wrist and hand; rheumatic, degenerative or neurological disease; partial or complete rotator cuff tear or other complex muscles of the shoulder joint; being in physical therapy or using orthosis for less than three months prior to research; positivity for lateral and medial epicondylitis tests;positivity in at least two of the following tests: Neer, Hawkins, painful arc between 60 ° and 120°, Jobe, infraspinatus test, apprehension test, replacement, sulcus sign, Rowe and Speed.

Design outcomes

Primary

MeasureTime frame
Measurement of pain intensity, obtained by Numeric pain Rating Scale. ;Measures of severity of symptoms and functional status, obtained by the Boston questionnaire score.

Secondary

MeasureTime frame
Measurements of pinch strength (tip to tip and tripod), obtained by the Pinch Gauge® dynamometer.;Surface electromyographic activity of the extensor carpi radialis and flexor carpi ulnaris muscles measured by Root Mean Square [RMS].

Countries

Brazil

Contacts

Public ContactDanielle;Helga Figueiredo;Tucci

Universidade Federal de São Paulo;Universidade Federal de São Paulo

dani.figueiredo16@yahoo.com.br;helgatucci@gmail.com+55 (013) 991662276;55 13 981588730

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 1, 2026