Skip to content

Investigating the effect of intervention on musculoskeletal disorders

Investigating the effect of the educational intervention program in the prevention of musculoskeletal disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240321061346N1
Enrollment
116
Registered
2024-04-10
Start date
2024-05-20
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Disorders. Other specified acquired deformities of musculoskeletal system

Interventions

The intervention group of educational packages includes a speech by an expert in health education and health promotion, an expert in occupational health and ergonomics, a presentation of pamphlets and

Sponsors

Tarbiat Modares University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Employees who want to participate in research. Employees who have access to the Internet and the ability to use mobile phones. Employees who have more than two years of experience in the petrochemical industry.

Exclusion criteria

Exclusion criteria: Having a second job. People who do not have musculoskeletal disorders caused by work. Having any musculoskeletal disorders with a pathological cause. Having any diseases or problems that prevent a person from participating in studying and doing sports exercises.

Design outcomes

Primary

MeasureTime frame
1. Work-related musculoskeletal disorders. Timepoint: Before the intervention, immediately after the intervention, three months after the intervention and six months after the intervention. Method of measurement: Nordic questionnaire and researcher-made questionnaire.

Secondary

MeasureTime frame
Pain caused by musculoskeletal disorders. Timepoint: Before the intervention, immediately after the intervention, three months after the intervention and six months after the intervention. Method of measurement: Visual analog scale.;Disability caused by pain. Timepoint: Before the intervention, immediately after the intervention, three months after the intervention and six months after the intervention. Method of measurement: Quebec Pain Disability Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Moradi

Tarbiat Modares University

zohre_moradi@modares.ac.ir+98 918 568 7572

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026