Effect of TDCS in patients with anterior knee pain syndrome
Not Applicable
Recruiting
- Conditions
- Patello femoral pain syndrome.
- Registration Number
- IRCT20210618051614N1
- Lead Sponsor
- niversity of social welfare and rehabilitation sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
Anterior knee pain with no history of surgery or trauma
No neurological diseases
Age between 20 and 40 years
Exclusion Criteria
People who do not want to cooperate
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before the intervention, after the end of treatment and 21 days after the start of treatment. Method of measurement: VAS.;Function. Timepoint: Before the intervention, after the end of treatment and 21 days after the start of treatment. Method of measurement: Kujala Questionnaire.;Balance. Timepoint: Before the intervention, after the end of treatment and 21 days after the start of treatment. Method of measurement: TOG balance test.
- Secondary Outcome Measures
Name Time Method