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- Klinische proef NCT02874950
Effective Methods of Reducing Lower Back, Neck and Shoulder Pain Among Office Workers
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).
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 1
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Working in office
Exclusion Criteria:
- Any physical or mental disease any surgery in background any limitation by Dr
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Diagnostisch
- Toewijzing: Gerandomiseerd
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Office exercise training
A package of exercise raining was defined by the researcher and one of the intervention group did it for 6 months.
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The exercise group, did 6 months office exercise training.
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Experimenteel: Ergonomic modification
The ergonomic group, followed 6 months ergonomic modification.
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The ergonomic modification group, followed 6 months modified office ergonomic modification.
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Experimenteel: Exercise and ergonomic
The mixture group, did 6 months exercise training and also followed 6 months ergonomic modification.
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The mixture group, did 6 months exercise training and also followed 6 months modified office ergonomic modification.
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Experimenteel: Control
Control group did not do any exercise and did not follow any ergonomic modification.
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Control group did not do any exercise and did not follow any ergonomic modification.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Measuring the prevalence of musculoskeletal disorder By Cornell questionniare
Tijdsspanne: Baseline
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The Cornell MSD Questionnaire was used to measure musculoskeletal discomforts.
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Baseline
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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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
Tijdsspanne: Change from Baseline musculoskeletal disorder at 6 months
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range of motion was measured by Goniometer.
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Change from Baseline musculoskeletal disorder at 6 months
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Medewerkers en onderzoekers
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Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
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Laatste update ingediend die voldeed aan QC-criteria
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Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- UPM/TNCPI/1.4.18.1(JKEUPM)/F2
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
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