Survey on low level laser in rehabilitatio
Not Applicable
- Conditions
- Musculoskeletal.muscular disordersM60-M61-M6
- Registration Number
- IRCT138905102995N2
- Lead Sponsor
- Vice chancellor for research, Semnan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
Girl students from the university dormitory, the age range 18-30 years, at least one trigger point on superior trapeze, the main complain on neck and shoulder without neurological signs,
Exclusion criteria: History of disc herniation in the neck, surgery, abnormal structure on neck and shoulder, presence of systemic diseases or pregnancy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain and neck range of motion. Timepoint: Before, after intervention; the period of intervention 2 weeks. Method of measurement: Visual analogue scale (VAS); goniometer.
- Secondary Outcome Measures
Name Time Method Range of motion of the upper limbs. Timepoint: Before, after intervention, the intervention period: 2 weeks. Method of measurement: The goniometer.