Study on the Effects of Trigger Point Dry Needling on Patients With Patello-femoral Pain Syndrome: A Randomized Controlled Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Patellofemoral Pain Syndrome
- Sponsor
- Riphah International University
- Enrollment
- 70
- Locations
- 1
- Primary Endpoint
- Goniometer
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
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.
Detailed Description
A double blinded Randomized Controlled Trial of 6 months study after the approval of synopsis, will be conducted. Convenience sampling technique will be used to enroll the patients. Patients will be selected according to predefined inclusion and exclusion criteria. All patients who fulfill inclusion criteria will be allocated in two group through randomization by lottery method. Group A will receive TrP-DN and group B will receive Sham Needling. Both groups will be asked to perform stretching exercise of Quadriceps daily after needling. The patients' outcomes will be measured by VAS for pain intensity and Kujala Questionnaire for functional status. The comparison between pre-treatment and post-treatment data will be done after 3 months. Informed consents will be taken from each patient. Data entry and analysis will be done with SPSS 23.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Both genders
- •Ages range from 18-40 years
- •They have clinical diagnosis of PFPS (the diagnosis was confirmed by a positive patellar grind test and tenderness of medial and lateral patellar facets)
- •Participants are also required to have a minimum pain score of 3 on Numeric Pain Scale
- •Kujala patellofemoral questionnaire score of 50 to 80 before the intervention.
- •Patients willing to participate
Exclusion Criteria
- •History of any following conditions
- •Participants who have received any treatment for PFPS within the 3 months
- •A history of lower extremities fracture or surgery
- •Presence of MSK diseases such as Acute Herniated Disc or Spondylolisthesis
- •History of any chronic disease e.g. Diabetes Mellitus
Outcomes
Primary Outcomes
Goniometer
Time Frame: 8th week
range of motion will be checked by Goniometer
Visual Analogue Scale
Time Frame: 8th week
Visual Analogue Scale
Kujala Questionnaire
Time Frame: 8th week
functional disability will be check by Kujala Questionnaire