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Clinical Trials/NCT02118246
NCT02118246
Completed
N/A

The Clinical Effects of Dry Needling & Kinesio Tape on Myofascial Trigger Point in the Vastus Lateralis Muscle in Subjects With PFPS

University of Social Welfare and Rehabilitation Science1 site in 1 country30 target enrollmentOctober 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Patellofemoral Pain Syndrome
Sponsor
University of Social Welfare and Rehabilitation Science
Enrollment
30
Locations
1
Primary Endpoint
Pain
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Patellofemoral Pain Syndrome(PFPS) is one of the most common health-related complaints in today's societies. Myofascial pain syndrome(MPS) have been attributed as the main cause and primary source of musculoskeletal pain. Trigger point of the vastus lateralis muscle may pull the patella superiorly and laterally, increasing compression of the patellofemoral joint during physical activities, result in PFPS and anterior knee pain. The purpose of this study was to investigate the effects of Dry Needling & kinesio tape on trigger point of vastus lateralis muscle in PFPS subjects.

Detailed Description

Pain intensity, pain pressure threshold and Disability of knee were collected at base line and at the end of treatment sessions.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
September 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Social Welfare and Rehabilitation Science
Responsible Party
Principal Investigator
Principal Investigator

Amir Massoud Arab

Dr.

University of Social Welfare and Rehabilitation Science

Eligibility Criteria

Inclusion Criteria

  • Presence of a palpable taut band in muscle.
  • Presence of a hypersensitive tender spot in the taut band.
  • Reproduction of the typical referred pain pattern of the trigger point in response to compression. To detect active trigger point, trigger point pressure tolerance was assessed using a mechanical pressure algometer. The investigator applied continuous pressure with the algometer with an approximate pressure of 2.5 kg/cm
  • Spontaneous presence of the typical referred pain pattern and/or patient recognition of the referred pain as familiar.
  • 5- Pain of at least 30 mm on a visual analogue scale (VAS) from 0 mm (no pain) to 100 mm (worst imaginable pain).

Exclusion Criteria

  • had a history of fracture of knee joint, dislocation of patella
  • previous knee or ankle surgery
  • had a history of neurologic condition
  • having physical therapy within the past month before the study
  • taking anticoagulants (e.g. warfarin)
  • local infection

Outcomes

Primary Outcomes

Pain

Time Frame: one year

Pain intensity using Visual Analogue Scale (VAS) were collected at base line and at the end of treatment

Secondary Outcomes

  • pain pressure threshold(one year)

Study Sites (1)

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