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comparison of two taping methods in patellofemoral pain syndrome

Comparison of efficiency of McConnell and kinesiology taping with Mc Connell method in patients with patellofemoral pain syndrome (PFPS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016040827287N1
Enrollment
36
Registered
2016-05-27
Start date
2014-11-22
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: For Mc Connell group, McConnell tape will immediately be attached over the affected patellar region, in the order of medial glide according to patellar orientation tests. The choice of
Treatment - Devices
Treatment - Other
For Mc Connell group, McConnell tape will immediately be attached over the affected patellar region, in the order of medial glide according to patellar orientation tests. The choice of taping methods
Kinesiology group: kinesiology tape as the McConnell tape will be attached over the affected patellar region, in the order of medial glide. To control lateral glide, one end of the tape is secured to
Control group: subjects in control group will be instructed to perform strengthening exercises employed at home. These include isometric vastus medialis oblique contraction while sitting with knee at

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age less than 40 years old; anterior or retro patellar pain, insidious in nature, which was aggravated by at least two of the following common functional activities of daily life: prolonged sitting, stair climbing, squatting, running, kneeling, hopping/ jumping; persistence for at least 3 months; lateral glide of patella; Exclusion criteria: any traumatic, inflammatory or infectious pathology in the lower extremity; dislocation and subluxation in the patellofemoral joint; history of surgery in the knee joint; any signs of secondary osteoarthritis in the knee joint; skin disorder or allergy after 24 hours; any deformity and fracture in the knee joint or lower extremity

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pre intervention, after intervention. Method of measurement: Visual Analog Scale.;Disability. Timepoint: Pre intervention, after intervention. Method of measurement: Kujala Patellofemoral Scale.;Functional limitation. Timepoint: Pre intervention, after intervention. Method of measurement: Modified Functional Index Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Rezaeian Ramsheh

Isfahan University of Medical Sciences

rezaeian_ramsheh@yahoo.com+98 31 3668 0048

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026