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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02874950
Other study ID # UPM/TNCPI/1.4.18.1(JKEUPM)/F2
Secondary ID
Status Completed
Phase Phase 1
First received August 11, 2016
Last updated August 19, 2016
Start date March 2016
Est. completion date August 2016

Study information

Verified date August 2016
Source Universiti Putra Malaysia
Contact n/a
Is FDA regulated No
Health authority Malaysia: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Background:Musculoskeletal discomforts (MSD), especially in the neck, lower back and shoulder areas, are some of the most common issues among office workers. The Social Security Organization (SOCSO) in Malaysia caps number of cases involving musculoskeletal injuries at a maximum of 10,000 per year.

Objectives: The primary aims of this research were to: 1. Measure the prevalence of MSD in a sample of office workers; 2. Test effective methods of reducing lower back, neck and shoulder pain in this sample by training exercise, or ergonomics modification, or both of them; and 3. Assess discomfort scores and the range of motion of the lower back, neck and shoulder muscles among the office workers after undertaking the different methods for a period of 6 months.

Methods: In a true experimental design, from 10,000 staff in Telecom Malaysia,onehundred and forty two office workers (of whom 50 were male), aged 20-50 y, were allocated randomly, from 3 different locations (Bangsar, Puchung, and Damansara), to one of three intervention groups (receiving training exercise, receiving modified ergonomics, receiving a combination of exercise and ergonomics modification) and a control group (receiving none of these interventions). The Cornell MSD Questionnaire was used to measure musculoskeletal discomforts, with focus on pain severity, before treatment and after 2, 4 and 6 months of the interventions. The range of motion (ROM) of the hip, neck, shoulder and knee were measured by a 12 inch goniometer, and the Borg CR10 scale was used to measure the perceived exertion of training exercises. The rapid office strain assessment (ROSA) questionnaire was used to assess the strain associated with office work. Height and weight were also measured to calculate the body mass index (BMI).


Description:

It is expected that, 6 months intervention including exercise training, ergonomic modification and mixture of these 2 intervention, maybe can decrease the severity of pain in lower back, neck and shoulder among office workers.


Recruitment information / eligibility

Status Completed
Enrollment 142
Est. completion date August 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Working in office

Exclusion Criteria:

- Any physical or mental disease any surgery in background any limitation by Dr

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
office exercise training
The exercise group, did 6 months office exercise training.
ergonomic modification
The ergonomic modification group, followed 6 months modified office ergonomic modification.
Exercise and ergonomic
The mixture group, did 6 months exercise training and also followed 6 months modified office ergonomic modification.
Control
Control group did not do any exercise and did not follow any ergonomic modification.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universiti Putra Malaysia

Outcome

Type Measure Description Time frame Safety issue
Primary Measuring the prevalence of musculoskeletal disorder By Cornell questionniare The Cornell MSD Questionnaire was used to measure musculoskeletal discomforts. Baseline No
Secondary Measure the effects of exercise training on decrease the musculoskeletal disorder by measuring the range of motion in neck, shoulder and lower back, and severity of pain will be measured by Cornell questionniare range of motion was measured by Goniometer. Change from Baseline musculoskeletal disorder at 6 months No
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