eg related exercises and medial tibial stress syndrome
Phase 3
- Conditions
- Medial tibial stress syndrome.
- Registration Number
- IRCT20170114031942N5
- Lead Sponsor
- Shahroud University of Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 50
Inclusion Criteria
Leg pain exertion caused by exercise, which lasts for several hours or days after exercise; Place of pain on the posterior-medial border of the tibia; incidence of pain during the palpation should be at least 5 cm; the nature of the diffuse pain in the palpation of the tibia, which is limited to the posterior- medial border of the bone, the rugged surface of the bone in the area of discomfort or pain in the tibia bone.
Exclusion Criteria
A history of paresthesia or other symptoms indicating legs pain caused by exercise (such as tibial fractures stress and chronic compartment syndrome); history of traumatic injury and lower limb surgery during the last 6 months; leg length difference.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dynamic arch index. Timepoint: Before the intervention and 12 and 24 weeks after the intervention. Method of measurement: By using of Footscan.;Dynamic distribution of plantar forces. Timepoint: Before the intervention and 12 and 24 weeks after the intervention. Method of measurement: By using of Footscan.;Foot and ankle muscle strength. Timepoint: Before the intervention and 12 and 24 weeks after the intervention. Method of measurement: Dynamometer.;Foot and ankle muscle endurance. Timepoint: Before the intervention and 12 and 24 weeks after the intervention. Method of measurement: Dynamometer.
- Secondary Outcome Measures
Name Time Method evel of physical activity in the previous week. Timepoint: Before the intervention, 12 and 24 weeks after the intervention. Method of measurement: 7-day Physical Activity Recall Questionnaire.;Level of impairment caused by injury. Timepoint: Before the intervention, 12 and 24 weeks after the intervention. Method of measurement: Using a numerical rating scale.;Activity limitations level. Timepoint: Before the intervention, 12 and 24 weeks after the intervention. Method of measurement: Using a numerical rating scale.;Perceived treatment effect. Timepoint: Before the intervention, 12 and 24 weeks after the intervention. Method of measurement: Using a patient perceived treatment effect questionnaire.