Effective Methods of Reducing Lower Back, Neck and Shoulder Pain Among Office Workers

August 19, 2016 updated by: Ardalan Shariat, Universiti Putra Malaysia

Effect of Exercise Training and Ergonomic Modification on Musculoskeletal Disorders Among Office Workers

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).

Study Overview

Detailed 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.

Study Type

Interventional

Enrollment (Actual)

142

Phase

  • Phase 1

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 50 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Working in office

Exclusion Criteria:

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Office exercise training
A package of exercise raining was defined by the researcher and one of the intervention group did it for 6 months.
The exercise group, did 6 months office exercise training.
Experimental: Ergonomic modification
The ergonomic group, followed 6 months ergonomic modification.
The ergonomic modification group, followed 6 months modified office ergonomic modification.
Experimental: Exercise and ergonomic
The mixture group, did 6 months exercise training and also followed 6 months ergonomic modification.
The mixture group, did 6 months exercise training and also followed 6 months modified office ergonomic modification.
Experimental: Control
Control group did not do any exercise and did not follow any ergonomic modification.
Control group did not do any exercise and did not follow any ergonomic modification.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measuring the prevalence of musculoskeletal disorder By Cornell questionniare
Time Frame: Baseline
The Cornell MSD Questionnaire was used to measure musculoskeletal discomforts.
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
Time Frame: Change from Baseline musculoskeletal disorder at 6 months
range of motion was measured by Goniometer.
Change from Baseline musculoskeletal disorder at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2016

Primary Completion (Actual)

July 1, 2016

Study Completion (Actual)

August 1, 2016

Study Registration Dates

First Submitted

August 11, 2016

First Submitted That Met QC Criteria

August 19, 2016

First Posted (Estimate)

August 22, 2016

Study Record Updates

Last Update Posted (Estimate)

August 22, 2016

Last Update Submitted That Met QC Criteria

August 19, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • UPM/TNCPI/1.4.18.1(JKEUPM)/F2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

We have not decided about it yet.

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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