About this trial
The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by non-probability convenient random sampling technique. Subjects in group A will receive functional motor control exercises. Group B will receive conventional exercises.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
male and female athlete within 19-40 years,
running a minimum average of 15 running kilometers,
Runners with one sided iliotibial band syndrome for at least 3 months were included,
Pain along IT band at either Gerdy's tubercle or the lateral femoral epicondyle during running,
Disqualifiers
Individuals with a history of previous knee trauma of past 6 months,
Individuals with a history of previous knee surgery of past 6 months,
Other knee abnormalities including patellofemoral joint pain,
popliteus tendinitis,
Trial design
Parallel
Treatments tested in this trial
Functional motor control excercise
Other interventionThis include functional motor control thrice a week for six weeks
convectional excercise
Other interventionThis include convectional exercise thrice a week for six weeks
Treatment groups
Trial outcomes
Primary outcomes
Numeric pain rating scale
pain will be assess by Numeric pain rating scale with minimum score 0 to maximum score 10
flexibility
flexibility will be assess by Y balance
lower extremity function
lower extremity function will be assess by lower limb extremity scale with score 0 to 80
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Sponsors and contacts
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