The Effects of Dry Needling & Kinesio Tape on Anterior Knee Pain
The Clinical Effects of Dry Needling & Kinesio Tape on Myofascial Trigger Point in the Vastus Lateralis Muscle in Subjects With PFPS
1 other identifier
interventional
30
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2012
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2013
CompletedFirst Submitted
Initial submission to the registry
April 16, 2014
CompletedFirst Posted
Study publicly available on registry
April 21, 2014
CompletedApril 21, 2014
April 1, 2014
7 months
April 16, 2014
April 16, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain
Pain intensity using Visual Analogue Scale (VAS) were collected at base line and at the end of treatment
one year
Secondary Outcomes (1)
pain pressure threshold
one year
Other Outcomes (1)
knee disability
one year
Study Arms (2)
Dry Needling
EXPERIMENTALThe taut band of trigger point in vastus lateralis muscle; localized between the thumb and index finger, was needled forward and backward repeatedly until there were no more local twitch response
Kinesio Tape
EXPERIMENTALY technique with 25% tension on the tails was applied. Direction of the technique was insertion to origin of the muscle and zone of the trigger point was placed at the center of Y strip.
Interventions
Dry needling was performed for one week, three times a week.
Kinesio tape was performed for one week, three times a week.
Eligibility Criteria
You may qualify if:
- 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/cm2.
- Spontaneous presence of the typical referred pain pattern and/or patient recognition of the referred pain as familiar.
- Pain of at least 30 mm on a visual analogue scale (VAS) from 0 mm (no pain) to 100 mm (worst imaginable pain).
You may not qualify if:
- 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
- pregnancy
- taking anticoagulants (e.g. warfarin)
- local infection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Social Welfare and Rehabilitation Sciences
Tehran, Islamic Republic of, 1985713831, Iran
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amir M Arab, PhD
University of Social Welfare and Rehabilitation Science
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
April 16, 2014
First Posted
April 21, 2014
Study Start
October 1, 2012
Primary Completion
May 1, 2013
Study Completion
September 1, 2013
Last Updated
April 21, 2014
Record last verified: 2014-04