Flexibility, Iliotibial Band Syndrome, Pain
Conditions
Keywords
motor control function excercise, lower extermity function, Iliotibial Band Syndrome
Brief summary
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.
Detailed description
The objective of this study is to determine the effects of functional motor control exercises on pain, flexibility and lower limb functional. It will be randomized controlled trial (RCT) research design at Pakistan sports board through non probability convenience sampling technique on 72 runners' athletes which will be allocated using random sampling through computerized generated number into Group A and Group B, 36 athletes will be in each group. Group A (interventional) will be given conventional training with functional motor exercise and Group B (control) will be given conventional training. There will be 3 sessions in a week for 6 weeks. The baseline scoring will be on 1st day, follow up will be taken at 6th week. Assessment will be made by Numeric pain rating scale, Lower extremity functional scale (LEFS), Single leg mini squat, Y balance. Data will be analyzed during SPSS software version 26. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two group
Interventions
OTHERFunctional motor control excercise
This include functional motor control thrice a week for six weeks
OTHERconvectional excercise
This include convectional exercise thrice a week for six weeks
Sponsors
Riphah International University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)
Masking description
assessor who will take reading is blind
Intervention model description
Randomized clinical trial
Eligibility
Sex/Gender
ALL
Age
19 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* 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, * positive stiffness with Ober's test, and * reporting pain during Noble's compression test.
Exclusion criteria
* 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, * lateral meniscal injury, * Degenerative joint disease, and * lateral collateral ligament sprain to the affected side.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Numeric pain rating scale | pre and 6 weeks post interventional | pain will be assess by Numeric pain rating scale with minimum score 0 to maximum score 10 |
| flexibility | pre and 6 weeks post interventional | flexibility will be assess by Y balance |
| lower extremity function | pre and 6 weeks post interventional | lower extremity function will be assess by lower limb extremity scale with score 0 to 80 |
Countries
Pakistan
Contacts
Primary ContactAmna Shahid, MS-DPT
Outcome results
None listed