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Iliotibial Band Syndrome clinical trials

View clinical trials related to Iliotibial Band Syndrome.

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NCT ID: NCT06410781 Not yet recruiting - Clinical trials for Iliotibial Band Syndrome

Effect of Radial Extracorporeal Shockwave Therapy on Ultrasonography Changes in Patients With Iliotibial Band Syndrome

ITB
Start date: May 20, 2024
Phase: N/A
Study type: Interventional

this study will be conducted to investigate the effects of radial extracorporeal shockwave therapy on ultrasonography changes, pain intensity, pain pressure threshold and lower limb function in patient with iliotibial band syndrome

NCT ID: NCT06269757 Not yet recruiting - Clinical trials for Iliotibial Band Syndrome

Exercise Program for ITB Syndrome

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

Patients with diagnosed iliotibial band (ITB) syndrome indicated for non-operative management will be randomized to individualized exercise program or standard physical therapy over the course of 3 months to determine any possible difference in clinical outcomes.

NCT ID: NCT06089005 Not yet recruiting - Clinical trials for Iliotibial Band Syndrome

Home-based Treatment Using the Sidekick Tool for Pain Relief in Patients With Iliotibial Band Syndrome

Start date: October 23, 2023
Phase: N/A
Study type: Interventional

The aim of the study is to test how well the Sidekick Tool works as a home-based pain relief for iliotibial band syndrome using instrument assisted soft tissue mobilization tool in healthy participants aged 18-65 years old. We hypothesize that the use of the tool over the course of seven days and by following a home-treatment plan will result in less pain that is caused by iliotibial band syndrome for the participants. Pain intensity will be measured using a Numerical Pain Rating Scale from 0-to-10. Other measurements will include pain intensity after exercise and if participants return to their sport. Participants will be asked to complete an online questionnaire to ensure they are a good fit for the study. Once they have been entered into the study, they will complete a video call with the researchers to go gather their current pain intensity levels. Participants will be emailed the instructions for how to use the tool for seven days and will be mailed the Sidekick Tool to their home. After seven days of using the tool, the participants will be asked to complete a final video call to gather their pain intensity levels. This number will be compared to their initial pain intensity to see if their pain has lowered while using the tool.