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.
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Numeric pain rating scale
Timeframe: pre and 6 weeks post interventional
flexibility
Timeframe: pre and 6 weeks post interventional
lower extremity function
Timeframe: pre and 6 weeks post interventional