Patellofemoral Pain Syndrome
Conditions
Keywords
Knee pain,Dry Needling, kinesioTape,Trigger point
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.
Interventions
DEVICEDry Needling
Dry needling was performed for one week, three times a week.
DEVICEKinesio Tape
Kinesio tape was performed for one week, three times a week.
Sponsors
University of Social Welfare and Rehabilitation Science
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
20 Years to 57 Years
Healthy volunteers
No
Inclusion criteria
1. Presence of a palpable taut band in muscle. 2. Presence of a hypersensitive tender spot in the taut band. 3. 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. 4. 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
1. had a history of fracture of knee joint, dislocation of patella 2. previous knee or ankle surgery 3. had a history of neurologic condition 4. having physical therapy within the past month before the study 5. pregnancy 6. taking anticoagulants (e.g. warfarin) 7. local infection
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain | one year | Pain intensity using Visual Analogue Scale (VAS) were collected at base line and at the end of treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| pain pressure threshold | one year | A pressure threshold algometer was used to measure the pain pressure threshold of a Trigger point of the vastus lateralis muscle before treatment and the end of treatment(after one week). |
Other
| Measure | Time frame | Description |
|---|---|---|
| knee disability | one year | The knee osteoarthritis outcome scale(KOOS) questionnaire was used to assess the knee disability. |
Countries
Iran
Outcome results
None listed