Investigating The Effects of Ergonomic Training Interventions Based on Precede-Proceed Model on musculoskeletal disorders And Stress In Surgical Technologists

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230422057974N1

Enrollment

Registered

2023-07-07

Start date

2023-12-10

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

Condition 1: Musculoskeletal Disorders. Condition 2: Stress.

Interventions

Intervention 1: Intervention group: Seven face-to-face training sessions will be held for surgical technologists. The duration of each seven sessions is 2 to 2.5 hours and the training will include t

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Having more than one year of work experience as a surgical technologist Desire to participate in the study

Exclusion criteria

Exclusion criteria: Having a history of surgery or any accident that affects the musculoskeletal area

Design outcomes

Primary

Measure	Time frame
Leveling the risk of not doing ergonomic work based on the Rapid Entire Body Assessment method. Timepoint: Risk stratification based on the Rapid Entire Body Assessment method before the intervention, 3 months and 6 months after the intervention. Method of measurement: Rapid Entire Body Assessment body condition assessment checklist.	—

Secondary

Measure	Time frame
Predisposing factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the precede - proceed model.;Enabling factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.;Enhancing factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.;Behavior score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.	—

Measure

Time frame

Predisposing factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the precede - proceed model.;Enabling factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.;Enhancing factors score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.;Behavior score. Timepoint: Before the start of the intervention, 3 and 6 months after the intervention. Method of measurement: The questionnaire of behavioral factors will be designed based on the asked-asked model.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMozhgan Amiri

Yazd University of Medical Sciences

mozhganamiri2345@gmail.com+98 26 3455 3193

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026