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Clinical Trials/IRCT20200818048446N1
IRCT20200818048446N1
Completed
未知

The effect of lumbopelvic manipulation on Electromyography parameters of gluteus medius and vastus medialis in patients with patellofemoral pain syndrome

Babol University of Medical Sciences0 sites26 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
patellofemoral pain syndrome.
Sponsor
Babol University of Medical Sciences
Enrollment
26
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • patients if they are aged less than 40 years
  • unilateral anterior knee pain or a pain on palpation of patellar facets provoked by at least two of these activities:ascending/descending stairs, squatting, prolonged sitting, jumping, kneeling and Isometric quadriceps contraction
  • positive sign in patellar apprehension test and/or eccentric step down test and/or vastus medialis coordination test
  • a pain level of at least 3 points and maximum 8 points on the numerical pain rating scale(NPRS) during resisted knee extension
  • knee disability level between 45 and 70 based on the Kujala patellofemoral questionnaire (KPQ)
  • Have at least 3 of the 5 criteria to predict treatment success, including the following: The difference in the active range of motion of the internal rotation of the hip between the two limbs is more than 14 degrees\- Dorsiflex active range of motion of the foot is more than 16 degrees\- No stiffnes after sitting for more than 20 minutes\- Navicular drop\- Squatting is most painful activity

Exclusion Criteria

  • a history of knee or spine surgery
  • dislocation or fracturein pelvic
  • meniscal lesion
  • patellar subluxation/dislocation
  • evidenceof tendinopathy or ligamentous pathologies
  • neurologic disorders
  • patients who had previously received physiotherapy treatment orused analgesic drugs within 72 h prior to the experiment
  • osteoporosis with documented compression fracture
  • severe lumbosacral nerveroot compression signs
  • systemic disease or connective tissue disorders

Outcomes

Primary Outcomes

Not specified

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