ClinicalTrials.gg
RecruitingNCT07831200Updated Sep 21, 2026

Effects of Mc Connell Versus Kinesio Taping; Combined With Hip and Knee Strengthening in Patients With Patellofemoral Pain Syndrome

An interventional study of Mc Connell tape and Kinesio taping in Patellofemoral Pain Syndrome, sponsored by Foundation University Islamabad. Recruiting at 1 site in Pakistan. Open to participants aged 26 Years to 44 Years. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Feb 2026, registered Sep 2026).
  • Started Feb 2026; still recruiting 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
26 Years to 44 Years
Sex
All
01

Study summary

Patellofemoral pain (PFP) is a common musculoskeletal-related condition that is characterized by insidious onset of poorly defined pain, localized to the anterior retro-patellar and/or peripatellar region of the knee. The onset of symptoms can be slow or acutely develop with a worsening of pain accompanying lower-limb loading activities (e.g. squatting, prolonged sitting, ascending/descending stairs, jumping, or running). This randomized controlled trial compares the effects of McConnell taping and Kinesio taping, each combined with a standardized hip and knee strengthening exercise program, in patients with Patellofemoral Pain Syndrome (PFPS). A total of 34 participants (17 per group), aged 26-44 years, will be randomly allocated into two groups. Both groups will undergo a 4-week intervention, consisting of supervised sessions on alternate days. Outcomes will be assessed at baseline and after the intervention. Group A will receive conventional physical therapy, hip and knee strengthening exercises, and McConnell taping. The intervention includes TENS, heating pad application, progressive strengthening exercises, functional training, stretching, and rigid McConnell taping applied before each session to provide medial patellar glide and improve patellar alignment. Group B will receive the same conventional physical therapy and strengthening program but with Kinesio taping. Elastic Kinesio tape will be applied using standardized I-strip and Y-strip techniques to facilitate patellar alignment, improve proprioception, and provide neuromuscular support. The tape may remain in place for 1-2 days, if tolerated. The primary outcomes include pain (Numeric Pain Rating Scale), range of motion (universal goniometer), and functional disability (KOOS-Patellofemoral questionnaire), measured at baseline and after the 4-week intervention.

Read the detailed description

This study is a randomized controlled trial (RCT) designed to compare the effectiveness of McConnell taping and Kinesio taping, when each is combined with a standardized hip and knee strengthening exercise program, in patients with Patellofemoral Pain Syndrome (PFPS). The trial aims to determine which taping technique provides greater improvements in pain, range of motion (ROM), and functional disability when used as an adjunct to exercise therapy. Participants will be recruited using a purposive sampling technique and randomly allocated into two intervention groups through the coin toss method. The study includes 34 participants, with 17 participants in each group, following adjustment for a 10% attrition rate. Adults aged 26-44 years, of either gender, meeting the inclusion criteria for PFPS will be enrolled. Outcome measures will be recorded at baseline and after completion of the 4-week intervention period. Participants allocated to Group A will receive conventional physical therapy, a structured hip and knee strengthening exercise program, and McConnell taping. Conventional physical therapy consists of Transcutaneous Electrical Nerve Stimulation (TENS) with a frequency of 50-100 Hz and a continuous cycle, combined with the application of a heating pad for 15 minutes before exercise. Additional treatment components include isometric and isotonic strengthening exercises for the hip and knee musculature, functional training, and stretching exercises prescribed according to the individual patient's needs. McConnell taping is performed using rigid, non-elastic tape applied over a protective adhesive underlay to minimize skin irritation. The tape is anchored from the lateral femoral condyle toward the medial posterior aspect of the knee to produce a medial glide of the patella, thereby improving patellar alignment and correcting maltracking during movement. Because of its rigid nature, the tape is applied before each treatment session and replaced during every supervised visit. The objective of McConnell taping is to reduce mechanical stress on the patellofemoral joint, improve knee biomechanics, decrease pain, and facilitate more effective performance of strengthening exercises. Participants in Group B will receive the same conventional physical therapy and identical strengthening program as Group A, ensuring that the only difference between groups is the taping technique. Instead of rigid taping, participants will receive Kinesio taping, which utilizes elastic therapeutic tape designed to provide dynamic support while allowing normal joint movement. The Kinesio taping technique consists of an I-strip applied over the tibial tuberosity without tension and a Y-strip positioned around the patella. The medial strip is applied with 25-40% stretch, whereas the lateral strip is applied with 75-100% mechanical stretch to provide stabilization and facilitate patellar alignment. Unlike McConnell tape, Kinesio tape may remain in place for 1-2 days, provided it is well tolerated, although participants will be instructed to remove the tape before going to bed. The elastic properties of Kinesio tape are intended to enhance proprioception, provide neuromuscular support, reduce pain, and improve movement without significantly restricting joint mobility.

Both intervention groups will participate in the same progressive hip and knee strengthening program, delivered over 4 weeks, with three supervised sessions per week, resulting in 12 treatment sessions. Each session will last approximately 30-40 minutes. The exercise protocol has been standardized to ensure consistency across groups while allowing the study to evaluate the independent effects of the two taping techniques. During Week 1, participants will perform isometric hip strengthening exercises including gluteal squeezes, heel presses, hip adduction squeezes, hip abduction presses, seated isometric hip flexion, and clamshell exercises. Each exercise will be completed in three sets of ten repetitions with a ten-second hold, followed by stretching according to patient requirements. The assigned taping technique will be applied before the exercise session. In Week 2, the program progresses to quadriceps sets, hamstring sets, wall sits, and knee extension holds, maintaining three sets of ten repetitions with ten-second holds. Stretching continues as needed, and taping is again applied before each treatment session. During Week 3, exercises advance to include lateral step-ups, squats limited to 0-45° of knee flexion, glute bridges, hip abduction raises, and clamshells performed using a light resistance band. Participants complete three sets of 10-12 repetitions, with stretching and taping continuing throughout the treatment period. In Week 4, resistance is further progressed through clamshells with resistance bands, wall slides, side-stepping with therabands, lateral step-ups, and banded glute bridges using light-to-moderate resistance. Stretching remains individualized, and the assigned taping intervention is applied before each supervised exercise session.

02

Conditions studied

  • Patellofemoral Pain Syndrome
03

In context

Patellofemoral Pain Syndrome

297 studies on the registry are indexed under Patellofemoral Pain Syndrome; 74 are open to participants now.

This study's planned enrollment of 34 is below the median of 45 across 244 interventional studies indexed under Patellofemoral Pain Syndrome.

Browse Patellofemoral Pain Syndrome studies →

Lead sponsor

Foundation University Islamabad is the lead sponsor of 255 studies on the registry; 142 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
26 Years to 44 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults 26-44 years of age
  • Both males and females
  • Subjects having anterior knee pain during (AKP) squatting or stair climbing/descending.
  • Chronic localized to the anterior retro-patellar and/or peripatellar region of the knee.
  • Positive outcomes of any two he following tests Eccentric Step Test Patellar Apprehension Test Squat test

Exclusion criteria

Exclusion Criteria:

  • History of therapy over 3 months
  • Diagnosed Chondromalacia Patellae
  • Diagnosed Plica Syndrome
  • Diagnosed Fat Pad Impingement
  • Patellar Dislocation
  • Diagnosed Arthritis (Osteoarthritis \& Rheumatoid Arthritis)
  • Traumatic Injuries: Ligament tears, meniscus tears, or fractures.
  • Prior knee surgery or invasive procedures (6 months)
  • Patients using blood thinners
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    Group A McConnell taping

    A stretchy adhesive fabric tape will be applied prior for base to prevent skin irritation then the Mc Connell tape will be applied by anchoring it lateral condyle of femur to medial posterior aspect of the knee to realign the patella by applying a medial patellar glide. The tape will be applied prior to each exercise session, maintained throughout the treatment session McConnell tape will be replaced each session due to rigidity The strengthening program will progress over four weeks from hip and knee isometric exercises, to hip and knee isotonic exercises followed by functional, resistance-based exercises and stretching.

    Procedure: Mc Connell tape

  • Experimental
    Group B Kinesio taping

    I strap without tension on tibial tuberosity horizontally and y strap for stabilizing and realigning patella with medial strap (25-40%) and lateral strap (75-100%) mechanical stretch. The strengthening program will progress over four weeks from hip and knee isometric exercises, to hip and knee isotonic exercises followed by functional, resistance-based exercises and stretching.

    Procedure: Kinesio taping

Interventions

  • ProcedureMc Connell tape

    A stretchy adhesive fabric tape will be applied prior for base to prevent skin irritation then the Mc Connell tape will be applied by anchoring it lateral condyle of femur to medial posterior aspect of the knee to realign the patella by applying a medial patellar glide. The tape will be applied prior to each exercise session, maintained throughout the treatment session McConnell tape will be replaced each session due to rigidity The strengthening program will progress over four weeks from hip and knee isometric exercises, to hip and knee isotonic exercises followed by functional, resistance-based exercises and stretching.

  • ProcedureKinesio taping

    I strap without tension on tibial tuberosity horizontally and y strap for stabilizing and realigning patella with medial strap (25-40%) and lateral strap (75-100%) mechanical stretch. The strengthening program will progress over four weeks from hip and knee isometric exercises, to hip and knee isotonic exercises followed by functional, resistance-based exercises and stretching.

06

What researchers measure

Primary outcomes

  1. Knee Pain

    Numerical Pain Rating Scale, Horizontal scale having numbers 0-10. 0 indicating no pain to 10 indicating worst pain

    Time frame: Baseline and after 4th week of treatment

  2. Hip and Knee Range of Motion

    Universal Goniometer will be used to assess the range of motion of hip and knee The baseline assessment will establish each participant's pre-intervention ROM values, which will serve as the reference (baseline) values for subsequent comparison, changes in hip and knee ROM from baseline to post-intervention will be determined within each group.

    Time frame: Baseline and after 4th week of treatment

  3. Functional Disability

    The Knee Injury and Osteoarthritis Outcome Score-Patellofemoral subscale (KOOS-PF) is an 11-item, patient-reported, disease-specific questionnaire generally scored on a 0-100 scale. A lower score indicates greater symptoms and functional limitations, whereas a higher score indicates better function and fewer symptoms.

    Time frame: Baseline and after 4th week of treatment

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07831200
Responsible party
Sponsor
First posted
Sep 21, 2026
Start date
Feb 13, 2026
Primary completion
Dec 19, 2026 (estimated)
Completion
Jan 18, 2027 (estimated)
Last update
Sep 21, 2026

Study contacts

Noor ul Hudda Saleem, DPT
Contact
huddasaleem1011@gmail.com
+92335-8577778
Muhammad Furqan Hassan, MS-OMPT
Contact
furqan.hassan@fui.edu.pk
051-5788171 ext. 733

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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