The effect of national academy of sports medicine training with ergonomic intervention on upper limb musculoskeletal disorders and upper cross syndrome in teachers

Effectiveness of sport exercises with ergonomic intervention on the reduction of upper extremity musculoskeletal disorders and upper cross syndrome of teachers

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180725040585N1

Enrollment

Registered

2019-01-08

Start date

2018-04-21

Completion date

Unknown

Last updated

2019-01-29

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

Conditions

musculoskeletal disorders. Disorder of muscle, unspecified

Interventions

Intervention 1: Intervention group: Receive NASM exercises and ergonomic interventions. Intervention 2: Control group: Doing daily and job activities.

Eligibility

Sex/Gender

All

Age

22 Years to 65 Years

Inclusion criteria

Inclusion criteria: having musculoskeletal disorders having upper cross syndrome

Exclusion criteria

Exclusion criteria: history of surgery or fracture joint diseases of the spine osteoporosis acute rheumatoid arthritis Congestive Heart Failure athletic activities

Design outcomes

Primary

Measure	Time frame
The amount of musculoskeletal disorders of the neck, shoulder and back. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Nordic Questionnaire and New York Test.;Forward head angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.;Forward shoulder angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.;Hyperkyphosis angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.	—

Measure

Time frame

The amount of musculoskeletal disorders of the neck, shoulder and back. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Nordic Questionnaire and New York Test.;Forward head angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.;Forward shoulder angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.;Hyperkyphosis angle. Timepoint: Before intervention and 3 months after intervention. Method of measurement: New York Test and UCS Software.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Karimian

The University of Isfahan

r.karimian@spr.ui.ac.ir+98 31 3793 2195

Outcome results

None listed

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