Musculoskeletal pain. Other disorders of the musculoskeletal system and connective tissue
Conditions
Interventions
Intervention 1: Intervention group: 3 Educational sessions
pamphlet and stretching. Intervention 2: Control group:This group does not receive any intervention.
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
7 Years to 13 Years
Inclusion criteria
Inclusion criteria: Elementary School Students (First to Sixth Grades) Complete informed consent by parents Students tend to participate in the study
Exclusion criteria
Exclusion criteria: Students who have birth defects. Students who are affected by reason of secondary cause such as accidents and else.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Musculoskeletal pain. Timepoint: 3 and 6 months after the intervention. Method of measurement: questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Posture. Timepoint: Before intervention, 3 and 6 months after the intervention. Method of measurement: Observation based on the standard checklist RULA.;Bag weight. Timepoint: Before intervention, 3 and 6 months after the intervention. Method of measurement: Measuring the weight of the bag with a scales.;Knowledge. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Perceived Susceptibility. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Perceived Severity. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Perceived Benefits. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Perceived Barriers. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Reinforcing Factors. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Self-efficacy. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire.;Enabling Factors. Timepoint: Before intervention, and 6 months after intervention. Method of measurement: Researcher made questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Gheysvandi
Hamedan University of Medical Sciences
Outcome results
None listed