Skip to content

The effect of Patellar Taping in Management of The Patellofemoral Pain Syndrome

The effect of Patellar Taping in Management of The Patellofemoral Pain Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111012851N2
Enrollment
30
Registered
2011-11-25
Start date
2011-11-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patellofemoral pain syndrome. Chondromalacia patellae

Interventions

Intervention 1: Control: Routin physiotherapy including: IR, Pain-relieving modalities, Ultrasound, Exercise therapy, Muscle stretching, Patellar mobilization, Patient education. Intervention 2: Inter
Rehabilitation
Control: Routin physiotherapy including: IR, Pain-relieving modalities, Ultrasound, Exercise therapy, Muscle stretching, Patellar mobilization, Patient education
Intervention: Patellar tapping in addition to Routin physiotherapy including: IR, Pain-relieving modalities, Ultrasound, Exercise therapy, Muscle stretching, Patellar mobilization, Patient education

Sponsors

Babol University of Medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with patellofemoral pain syndrome. Exclusion criteria: Patients with knee pain due to other injuries such as fractures, meniscal and ligamentum injuries.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Befor & After intervention. Method of measurement: Visual Analogue Scale.;Lateral Patellofemoral Angle. Timepoint: Befor & After intervention. Method of measurement: Radiography.;Lateral Patellar Displacement. Timepoint: Befor & After intervention. Method of measurement: Radiography.;Patellofemoral Congruency Angle. Timepoint: Befor & After intervention. Method of measurement: Radiography.

Secondary

MeasureTime frame
Functional disability. Timepoint: Befor & After intervention. Method of measurement: KOOS questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Taghipour Darzi

Babol University of Medical Sceinces

taghipourm@yahoo.com , taghipour@mubabol.ac.ir+98 11 1219 9591

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 9, 2026