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Design and Evaluation of Training of Low Back Pain Prevention Behaviors based on PRECEDE-PROCEDE Model and its Evaluation based on REAIM Model in Health workers in Shahid Beheshti University of Medical Sciences

Effect of Training of Low Back Pain Prevention Behaviors based on PRECEDE-PROCEDE Model and its Evaluation based on REAIM Model in Health workers in Shahid Beheshti University of Medical Sciences: A Double-blinded Randomized Controlled Trial.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190811003
Enrollment
120
Registered
2019-08-11
Start date
2019-12-03
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

no problems Back Pain&#44

Interventions

Effect of Training of Low Back Pain Prevention Behaviors based on PRECEDE&#45
PROCEDE Model and its Evaluation based on REAIM Model An educational program based on the constructs of the prescriptive theory and LMS (virtual training on pain relief methods.The intervention group
Experimental Behavioral,No Intervention No treatment
Educational intervention group: First,No intervention group

Sponsors

Fund for the Protection of Researchers of the Country
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Health care workers who are willing to participate in the study, attend classes and tend to use mobile or computer software.

Exclusion criteria

Exclusion criteria: Have any illness or problems that prevent a person from participating in studying and practicing Lack of computer or mobile skills

Design outcomes

Primary

MeasureTime frame
,Change preventive behaviors of low back pain at befor,after 6,12 months after end of the intervention RE-AIM and PRECEDE-PROCEDE Model Questionaire—

Secondary

MeasureTime frame
Reduce Chronic Low Back Pain at befor,after 6,12 months after end of the intervention Quebec back pain and VAS (Visual Analogue Scale) questionnaire, increase Quality of Life at befor,after 6,12 months after end of the intervention SF- 36 Questionaire—

Countries

iran

Contacts

Public ContactDr. Afshin Zarghi

Vice chancellor for research,Assistant Professor of Health Affairs,Shahid Beheshti University of Med

INFO@sbmu.ac.ir+98 21 23871

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026