- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04857853
Exercise, Rest Breaks and Ergonomics Modification on Fatigue and MSK Discomfort in Static Workstation
Effects of Exercise, Rest Breaks and Ergonomics Modification on Fatigue and Musculoskeletal Discomfort in Static Workstation Office Workers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Static workstation workers frequently experience musculoskeletal discomfort which, according to a survey of the literature, may include muscle tension, muscle fatigue, paresthesia, pain, and/or physical strain in soft tissues and bones. The incidence of musculoskeletal discomfort in office workers like computer users is as high as 50%. In various studies on static workstation workers, musculoskeletal discomfort has been reported, either separately or in aggregate, in the neck, shoulders, elbows, wrists, hands, back, legs, buttocks, ankles, feet, and chest.
The current study examines the effects of exercise, ergonomic modifications, and rest breaks on fatigue and musculoskeletal discomfort during computer tasks. For the purpose of this project, musculoskeletal discomfort is defined as a constellation of signs and symptoms that include muscle tension, paresthesia, pain, and/or physical strain in soft tissues and bones.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Islamabad, Punjab, Pakistan
- Foundation University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Both male and female
- Age: 25-45 years
- Those static workstation office workers using a computer for at least 6 hours per day.
- Static workstation office workers screened by ROSA.
Exclusion Criteria:
- Discomfort from non-musculoskeletal origin
- Recent history of trauma and receiving any kind of treatment for the current condition
- Severe orthopedic disease
- Any mental and physiological illness that could interfere in the exercise
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise Without Rest Breaks
|
Participants in the exercise group will receive 'Exercise Breaks', of 10 minutes, twice a day during the work hours, in addition to the two 'Conventional Rest Breaks' of 15 minutes, twice a day during the work hours. Exercises include shoulder shrugs, neck tilts, wrist and forearm stretch, back and hip stretch, upper body stretch, hamstring stretch, upper back stretch, hand/finger stretch. Side stretch and neck stretch. Follow up 3 times a week for 5 weeks. |
Experimental: Exercise With Rest Break
|
Participants in the exercise with rest break group will receive 'Exercise Breaks', of 10 minutes, twice a day during the work hours, in addition to the two 'Conventional Rest Breaks' of 15 minutes, twice a day during the work hours. Participants will also receive 'Supplemental Micro Breaks', of 30 seconds after every 15 minutes of working on a static computer workstation Follow up 3 times a week for 5 weeks. |
Experimental: Rest Break
|
Participants in the rest breaks group will receive 'Supplemental Micro Breaks', of 30 seconds after every 15 minutes of working on a static computer workstation in addition to the two 'Conventional Rest Breaks' of 15 minutes twice a day during the work hours. Follow up 3 times a week for 5 weeks. During the rest breaks, participants will not perform any exercises. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cornell Musculoskeletal Discomfort Questionnaire
Time Frame: 6th week
|
To assess the severity of musculoskeletal discomfort.
minimum as Never = 0, and maximum as Several times every day = 10 The discomfort score is the severity of discomfort categorized as 'mild', 'moderate', and 'severe discomfort'.
|
6th week
|
Chalder fatigue scale
Time Frame: 6th week
|
Each of the 11 items is answered on a 4-point scale ranging from the asymptomatic to maximum symptomology, such as 'Better than usual', 'No worse than usual, 'Worse than usual, and 'Much worse than usual.
|
6th week
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Tarwaka P, Bakri LS. Ergonomi Industri Dasar-dasar pengetahuan ergonomi dan aplikasi di tempat kerja. Surakarta: Harapan Press; 2010.
- Daneshmandi H, Choobineh AR, Ghaem H, Alhamd M, Fakherpour A. The effect of musculoskeletal problems on fatigue and productivity of office personnel: a cross-sectional study. J Prev Med Hyg. 2017 Sep;58(3):E252-E258.
- Rahimi R. Effect of different rest intervals on the exercise volume completed during squat bouts. J Sports Sci Med. 2005 Dec 1;4(4):361-6. eCollection 2005 Dec.
- Barredo RDV, Mahon K. The effects of exercise and rest breaks on musculoskeletal discomfort during computer tasks: An evidence-based perspective. Journal of Physical Therapy Science. 2007;19(2):151-63.
- Willardson JM, Burkett LN. A comparison of 3 different rest intervals on the exercise volume completed during a workout. J Strength Cond Res. 2005 Feb;19(1):23-6. doi: 10.1519/R-13853.1.
- Menzel NN, Brooks SM, Bernard TE, Nelson A. The physical workload of nursing personnel: association with musculoskeletal discomfort. Int J Nurs Stud. 2004 Nov;41(8):859-67. doi: 10.1016/j.ijnurstu.2004.03.012.
- Hamberg-van Reenen HH, van der Beek AJ, Blatter BM, van der Grinten MP, van Mechelen W, Bongers PM. Does musculoskeletal discomfort at work predict future musculoskeletal pain? Ergonomics. 2008 May;51(5):637-48. doi: 10.1080/00140130701743433.
- Hou JY, Shiao JS. Risk factors for musculoskeletal discomfort in nurses. J Nurs Res. 2006 Sep;14(3):228-36. doi: 10.1097/01.jnr.0000387581.04716.56.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/00858 Anam Rehman
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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