Skip to main content
Clinical Trials/NCT07447219
NCT07447219
Recruiting
Not Applicable

The Effectiveness of Ergonomics Intervention Program to Reduce the Risk Factors of Musculoskeletal Symptoms Among Dubai Healthcare Workers in Dubai (UAE)

Universiti Putra Malaysia1 site in 1 country110 target enrollmentStarted: March 1, 2024Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
110
Locations
1
Primary Endpoint
Change in Musculoskeletal Disorders

Overview

Brief Summary

This study evaluates an ergonomics intervention to reduce work-related musculoskeletal disorders (MSDs) among dental healthcare workers in Dubai government hospitals, where up to 90% prevalence affects the lower back, neck, shoulders, and upper extremities due to repetitive tasks and postures. Using a cluster randomized controlled trial (RCT) across three hospitals (55 participants per intervention/control group), it assesses MSD prevalence/severity, mental health, physical activity, and KAP scores at baseline, post-intervention, and three-month follow-up. Analyses include logistic regression, ANOVA, and GEE. Expected outcomes: identify predictors and demonstrate intervention efficacy via education, environmental, and behavioral changes, informing UAE occupational health policies.

Detailed Description

The study aims to evaluate the effectiveness of an ergonomics intervention program to reduce work-related musculoskeletal disorders (MSDs) among dental healthcare workers in Dubai government hospitals. MSDs pose significant occupational health challenges globally, especially among dental professionals, who often experience high prevalence of pain in the lower back, neck, shoulders, and upper extremities due to repetitive tasks, static postures, and patient handling. In Dubai and the broader UAE, these disorders affect up to 90% of dental healthcare workers, yet focused research and intervention programs remain limited. This research will be conducted in three phases. A cluster randomized controlled trial (RCT) will be conducted to evaluate the intervention's effectiveness by comparing outcomes between intervention and control groups at baseline, post-intervention, and a three-month follow-up. Outcome measures include changes in MSD prevalence and severity, mental health impact, physical activity level, and KAP scores. Statistical analyses will include logistic regression, one-way ANOVA, and Generalized Estimating Equations to assess within- and between-group differences over time. This RCT will recruit 110 participants (55 per group), using cluster randomization of hospitals to prevent contamination. Participants must have at least one year of professional experience and be between 25 and 65 years old, excluding those with certain medical conditions or current leave. Expected outcomes include identifying significant socio-demographic, mental health, physical activity, and environmental predictors for MSDs, and demonstrating the intervention's effectiveness in reducing MSD risk factors and improving related health and behavioral outcomes. The study emphasizes the integration of ergonomic education with environmental and behavioral modifications to achieve sustainable improvements in dental workers' occupational health. This research addresses critical gaps in understanding and managing MSDs among dental healthcare workers in Dubai, providing evidence-based guidance for occupational health policies and practices. Its comprehensive, theory-driven intervention program has the potential to enhance the well-being, productivity, and retention of dental professionals, ultimately benefiting patient care quality in the rapidly growing UAE healthcare sector.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
25 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Dental healthcare workers currently active in their professional roles.
  • Minimum of one year of professional experience to ensure adequate occupational exposure.
  • Age range between 25 and 65 years to focus on the working-age population most at risk.
  • Consent to participate in the study.

Exclusion Criteria

  • Individuals on extended leave or not currently practicing.
  • History of upper limb injuries unrelated to work.
  • Presence of neurological or rheumatological conditions.
  • Severe systemic diseases such as multiple sclerosis or stage II hypertension.
  • Recent surgeries involving the neck or shoulder.
  • Pregnancy.

Arms & Interventions

Educational intervention program

Other

The intervention group will receive an educational intervention program to reduce and changes in work-related musculoskeletal disorders (MSDs), Mental Health, Physical Activity, Knowledge, Attitude and Practice about Work-Related MSDs.

Intervention: Educational intervention program to reduce work-related musculoskeletal disorders (MSDs) (Other)

No Intervention: Control group

No Intervention

The control group will not any educational intervention program

Outcomes

Primary Outcomes

Change in Musculoskeletal Disorders

Time Frame: T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.

Will be assessed via the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ; Hedge et al., 1999). Participants will self-report frequency (Never-Always), severity (Slight-Extreme), and interference (Likert scales) across body regions (neck, shoulders, back, limbs). The total score will be calculated as frequency × severity × interference.

Secondary Outcomes

  • Improve in Mental Health(T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.)
  • Improve in Physical Activity(T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.)
  • Improve in Knowledge of Work-Related MSDs(T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.)
  • Improve in Attitude toward Work-Related MSDs(T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.)
  • Improve in Practice regarding Work-Related MSDs(T1 = Baseline. T2= One month's post-intervention. T3= Three months Follow up.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

FARAH ALI ABDULLA ALHAMMADI

Principal Investigator

Universiti Putra Malaysia

Study Sites (1)

Loading locations...

Similar Trials