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Whole body electrical muscle stimulation in patellofemoral pain syndrome

Not Applicable
Recruiting
Conditions
Patellofemoral pain syndrome.
Patellofemoral disorders
M22.2
Registration Number
IRCT20220421054600N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

Young women with a gradual onset of anterior knee pain without a history of trauma for at least 6 months.

Exclusion Criteria

Any intra-articular symptoms such as ligament and meniscal injury.
Existence of pain and tenderness in the patellar tendon, the internal hamstring tendon , ilio tibial band.
Osgood Schlatter or Sinding Larsen-Johansson syndrome.
Referral pain of hip and lumbar.
History of patellar dislocation.
History of previous surgery on the patellofemoral joint.
Existence of signs of degeneration in radiographic finding.
Taking corticosteroids and anti-inflammatory drugs.
Having a pacemaker, implant .
Pregnancy.
Epilepsy.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score in the visual analogue scale. Timepoint: Measurement of pain at the beginning of the study, seven weeks and three months after starting interventions. Method of measurement: Visual analogue scale.;Function(strength). Timepoint: Measurement of function (strength ) at the beginning of the study, seven weeks and three months after starting interventions. Method of measurement: Dynamometer.;Function (Step down test). Timepoint: Measurement of function (step down test ) at the beginning of the study, seven weeks and three months after starting interventions. Method of measurement: The number of repetitions.;Function(muscle endurance). Timepoint: Measurement of function (muscle endurance) at the beginning of the study, seven weeks and three months after starting interventions. Method of measurement: time.
Secondary Outcome Measures
NameTimeMethod
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