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The Effect of Working Hardening Program for Return-to-Work for Workers with Low Back Pain - Article


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Back Pain

Back Injuries; Pain, Back




Clinical Trial: The Effect of Working Hardening Program for Return-to-Work for Workers with Low Back Pain

This study is currently recruiting patients.
Verified by National Taiwan University Hospital August 2002

Sponsored by: National Taiwan University Hospital
Information provided by: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT00155662

Purpose

Occupational injury results in family economic crisis and national productivity loss, it is really becoming an important issue in our society. Low back pain is the most frequent injury affecting the workers. Except of prevention of injury, to have a work-hardening program and to push the injured workers return to work is also a challenge of medical personnels. The purposes of this study are (1) to develop a guideline to assess the low-back-pain workers’ impairment and working capacity; (2) to formulate a feasible work-hardening program for the low-back-pain workers; and (3) to execute the program, evaluate the training effect and then follow up the rate of return-to-work of the low-back-pain workers.

In the first year, a guideline of assessment of low- back impairment and working capacity will be developed. It may consist of the demographic data, the working status, the physical need in work, trunk muscle isokinetic strength, Oswestry low bak disability questionnaire, functional capacity evaluation and quality of life questionnaire. The whole assessment package will be empirically applied in low-back-pain workers and the validity and reliability will be tested. Besides, a work-hardening program for the low-back-pain workers will be established in the first year through the expert meeting and literature review. The work-hardening program will consist of training of trunk muscle strength, flexibility, and general fitness. A sling-exercise-training model will be applied in the program. From the second year, low-back-pain workers in outpatient department will be recruited with their own agreement and grouped randomly into the work-hardening group or the control group. The expected number is 30 in each group. According to the result of assessment of impairment and working capacity, the workers in work-hardening group will start the individualized work-hardening program for 3 months. After the program, the workers will be assessed again to evaluate the training effect, and, we will follow the rate of return-to-work among them three and 6 months after the program. The workers in the control group will be followed at 6 and 9 months after the enrollment and to get the rate of return-to-work in this group.

Condition Intervention
Chronic Low Back Pain Over 3 Months
 Behavior: work hardening program

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Educational/Counseling/Training, Non-Randomized, Open Label, Active Control, Parallel Assignment, Safety Study

Further Study Details: 
Primary Outcomes: functional capacity evaluation, Oswestry disability index
Secondary Outcomes: low back pain, work hardening
Expected Total Enrollment:  60

Study start: August 2002;  Expected completion: July 2004
Last follow-up: July 2004;  Data entry closure: July 2004

Occupational injury results in family economic crisis and national productivity loss, it is really becoming an important issue in our society. Low back pain is the most frequent injury affecting the workers. Except of prevention of injury, to have a work-hardening program and to push the injured workers return to work is also a challenge of medical personnels. The purposes of this study are (1) to develop a guideline to assess the low-back-pain workers’ impairment and working capacity; (2) to formulate a feasible work-hardening program for the low-back-pain workers; and (3) to execute the program, evaluate the training effect and then follow up the rate of return-to-work of the low-back-pain workers.

In the first year, a guideline of assessment of low- back impairment and working capacity will be developed. It may consist of the demographic data, the working status, the physical need in work, trunk muscle isokinetic strength, Oswestry low bak disability questionnaire, functional capacity evaluation and quality of life questionnaire. The whole assessment package will be empirically applied in low-back-pain workers and the validity and reliability will be tested. Besides, a work-hardening program for the low-back-pain workers will be established in the first year through the expert meeting and literature review. The work-hardening program will consist of training of trunk muscle strength, flexibility, and general fitness. A sling-exercise-training model will be applied in the program. From the second year, low-back-pain workers in outpatient department will be recruited with their own agreement and grouped randomly into the work-hardening group or the control group. The expected number is 30 in each group. According to the result of assessment of impairment and working capacity, the workers in work-hardening group will start the individualized work-hardening program for 3 months. After the program, the workers will be assessed again to evaluate the training effect, and, we will follow the rate of return-to-work among them three and 6 months after the program. The workers in the control group will be followed at 6 and 9 months after the enrollment and to get the rate of return-to-work in this group.

Eligibility

Ages Eligible for Study:  18 Years   -   65 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • aged 18 to 65years have a job low back pain

Exclusion Criteria:

-

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00155662

J Y Tsauo, PhD      886-2-23123456 

Taiwan
      National Taiwan University Hospital, Taipei,  100,  Taiwan; Recruiting
J Y Tsauo, PhD  886-2-23123456 

Study chairs or principal investigators

J Y Tsauo, PhD,  Study Director,  Grad School of PT, College of Medicine, NTU   

More Information

Study ID Numbers:  9100002906
Last Updated:  September 9, 2005
Record first received:  September 9, 2005
ClinicalTrials.gov Identifier:  NCT00155662
Health Authority: Taiwan: Department of Health
ClinicalTrials.gov processed this record on 2005-09-13

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Page Updated: October 3, 2005
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