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The effect of ergonomics orientation and motor control exercises in patients with work-related upper extremity disorders (WRUED)

Randomised and controlled study of the effect of ergonomics orientation and motor control exercises in patients with WRUED

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN28200443
Enrollment
60
Registered
2010-04-29
Start date
2010-08-20
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Work-related upper extremity disorders (WRUED) Injury, Occupational Diseases, Poisoning

Interventions

A group will receive ergonomics orientation and another will receive ergonomics orientation and motor control training for movement re-education. Both groups will be followed-up for 4 weeks and will b

Sponsors

Federal University of Juiz de Fora (Brazil)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients, either sex, aged between 20 and 55, with specific or non specific WRUED who complain about pain in the cervical area, shoulders, elbow, forearm, wrist and hands and have difficulty to make work-related as well as daily life movements for at least 6 months. 2. Patients who have agreed to interrupt the traditional physiotherapeutic treatment and to participate in this study for 4 weeks. 3. Patients who have painless movement in at least 60% of the normal range of movement of the glenohumeral joint for flexion and rotation.

Exclusion criteria

Exclusion criteria: 1. Patients in the acute stage, which is defined by flogistic signs and limitation of the range of movement in the initial angles due to pain. 2. Patients submitted to surgery due to WRUED. 3. Patients with established diagnosis of the following: 3.1. Cervical discopathies 3.2. Neurological diseases 3.3. Fibromyalgia and rheumatic diseases 3.4. Cancer 3.5. Severe psychiatric disease 3.6. Pregnancy 3.7. Hypermobility syndrome

Design outcomes

Primary

MeasureTime frame
Pain, assessed through the Visual Analogue Pain Scale (VAS)

Secondary

MeasureTime frame
Work Ability Index validated in Brazil

Countries

Brazil

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026