Medial tibial stress syndrome.
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: In addition to anti-pronation foot orthoses, this group also receives an exercise training intervention. Exercise training intervention is focus
Sponsors
Shahroud University of Technology
Eligibility
Sex/Gender
Male
Age
18 Years to 35 Years
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Level 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAynollah Naderi
Shahrood University of Technology
Outcome results
None listed