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The Effect of Adding Tecartherapy On routine physicalTherapy On Pain And Kinetic Changes In Runners With Medial Tibial Stress Syndrome

The Effect of Adding Tecartherapy On routine physicalTherapy On Pain And Kinetic Changes In Runners With Medial Tibial Stress Syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220301054160N1
Enrollment
40
Registered
2022-04-08
Start date
2022-04-20
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Medial Tibial Stress Syndrome. Other injury of other muscles and tendons at lower leg level

Interventions

Intervention 1: Intervention group: Tecar treatment group, 9 sessions of tecar therapy, the total time of treatment with tecar intervention in this study will be 15 minutes, which will be used as 5 m

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Subjects of any gender People aged 20-40 years. Have a history of pain during exercise in the inner-posterior part of the tibia bone and the pain spreads by touching the posterior-inner edge of the tibia about 5 cm in place Existence of pain that occurs with exercise and occurs during and after exercise The presence of pain in the affected leg is predominan Have this pain for at least a week

Exclusion criteria

Exclusion criteria: Patients with current or previous radiological symptoms of stress fractures or other types of fractures Local infection or osteomyelitis in the same foot Tumor in the area Previous surgery on the same leg Previous use of tecartherapy to treat tibial internal stress syndrome. Pregnancy Disorder and numbness in the area Patients with balance disorders, patients with middle ear disorder

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: In the first session and after the completion of 9 treatment sessions. Method of measurement: Visual scale of pain.;Measurement of ground reaction force. Timepoint: In the first session and after the completion of 9 treatment sessions. Method of measurement: Force plate.;Measuring the average displacement velocity. Timepoint: In the first session and after the completion of 9 treatment sessions. Method of measurement: Force plate.;Measure the amount of displacement. Timepoint: In the first session and after the completion of 9 treatment sessions. Method of measurement: Force plate.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsaeideh Babaeitabar

Semnan University of Medical Sciences

saeidehbabaei66@gmail.com+98 23 3344 8999

Outcome results

None listed

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