A double blinded clinical controlled trial will be performed on individuals with patello femoral pain syndrome in which Trigger Point Dry Needling will be given to experimental group while Sham Needling will be given to the control group, targeting the trigger points present in the Quadriceps of affected individuals assessing the pain,functional disability and range of motion of the affected individuals.
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Visual Analogue Scale
Timeframe: 8th week
Kujala Questionnaire
Timeframe: 8th week
Goniometer
Timeframe: 8th week