Efficacy of Telerehabilitation Intervention Program Using Telebiofeedback Among Computer Operators

Sponsor
Sheba Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT01178983
Collaborator
(none)
50
1
2
14
3.6

Study Details

Study Description

Brief Summary

In the recent decades, with technology development, computer workstation has become fundamental both at work and at home environments, and is now used routinely for many purposes. Musculoskeletal disorders (MSD) are most often characterized by backaches, neck and upper extremities pain, discomfort and pain in joints, muscles and soft tissues. Since it has been found that many musculoskeletal disorders are connected, among others, to biomechanical and psychosocial factors relating to a person's work environment, the literature refers to them as Work Related MSD (WRMSD). Risk factors correlated with WRMSD include repetitive motions, awkward positions or static muscle loading over prolonged periods of time, use of high keystroke force, direct mechanical pressure, vibration and extreme temperatures. Computer operators found to be sitting statically for a long time in front of the computer and keyboard, with limited options of changing body position. Psychosocial factors have also been implicated in the workstation musculoskeletal disorders with computer operators. Workers with WRMSD may suffer from persistent pain, loss of function and work disability. Therefore, it may include changes in the employment and earnings for injured workers. The complex nature of these injuries suggests that workplace rehabilitation interventions are a crucial aspect of treatment management.

The main objective of this study is to explore the use of biofeedback intervention, based on tele-rehabilitation principle, with computer operators suffer from WRMSD. Treatment efficacy will be tested by use of RULA (Rapid Upper Limb Assessment) method. Data analysis will be done by ANOVA Repeated Measures.

Hypothesis: Biofeedback intervention, based on tele-rehabilitation principle, will be found effective with computer operators suffer from WRMSD.

Condition or Disease Intervention/Treatment Phase
  • Device: surface electromyography
  • Device: surface electromyography
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Study Start Date :
Aug 1, 2010
Anticipated Primary Completion Date :
Oct 1, 2011
Anticipated Study Completion Date :
Oct 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: telebiofeedback

Device: surface electromyography
Surface electromyography (SEMG) telebiofeedback

Active Comparator: biofeedback

Device: surface electromyography
conventional biofeedback

Outcome Measures

Primary Outcome Measures

  1. Posture at work environment measured by Rapid Upper LImb Assessment (RULA) [15 months]

Secondary Outcome Measures

  1. Musculoskeletal Disorders (MSD) - pain and inconvenience [15 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • computer operators who spend more than 4 hours a day working with computer

  • computer operators who suffer from pain and inconvenience or injury in upper limbs, such as Lateral Epicondylitis, de Quervain disease, Carpal Tunnel Syndrome (CTS), Ulnar Tunnel Syndrome, Flexor-Extensor peritendinitis or teno-synovitis of the forearm-wrist region.

Exclusion Criteria:
  • subjects who suffer from neurological injuries

  • subjects who suffer from orthopedic injuries or other metabolic or autoimmune diseases, that cause joint oedema or hand numbness (pregnancy, diabetes, heart disease and arthritis).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sheba Tel Hashomer hospital - upper limb rehabilitation center Ramat Gan Israel 52621

Sponsors and Collaborators

  • Sheba Medical Center

Investigators

  • Study Chair: Merav Golombowicz, BOT, Upper Limb Rehabilitation Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01178983
Other Study ID Numbers:
  • SHEBA-10-7334-RP-CTIL
First Posted:
Aug 10, 2010
Last Update Posted:
Jun 21, 2011
Last Verified:
Jun 1, 2011

Study Results

No Results Posted as of Jun 21, 2011