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Not yet recruitingNCT07909694Updated Nov 2, 2026

McGill Core and Proprioception Training in Runner's Knee.

An interventional study of McGill Core stability exercises and Proprioception Training in Runner's Knee, sponsored by University of Management and Technology Lahore. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by University of Management and Technology Lahore · Not applicable, Interventional, and Treatment

Updated Nov 2, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

Runner's knee, most common condition causing knee pain; is defined by pain around or behind patella in young and physically active individuals. Runner's knee affects 25 to 40% knee patients reported in sports clinic. Exact pathology is unknown but factors such as trauma, overuse, muscular imbalance and maltracking of patella may be involved in causing symptom of runner's knee may continue to increase over years if unmanaged such as limitations in functional activities and poor quality of life. Patient suffering from runner's knee often shows weakness or inactivation of major muscles. A variety of different types of exercise have been explored to treat runner's knee, including neuromuscular training which restores movements by increasing strength, sensorimotor control and stability. However, in this research we will study McGill core and proprioception training effects on runner's knee patients. Objective of this study will be to compare effects of McGill core and proprioception training on balance, agility, deceleration and knee function in athletes with runner's knee. Study design will be randomized clinical trial. Evaluation will be done by using KUJALA, Star Excursion Test, Single leg stance Test, Agility T test and Functional Hop test. Non-probability convenient sampling will be used and the subjects will be allocated to two groups by random allocation. Group A will receive McGill core exercises and Group B will receive Proprioception exercises. Both groups will receive hot pack for 10 minutes as basic treatment of knee pain before techniques application. Both groups will receive 16 sessions for the period of 4 weeks. Measurements of all the outcome variables will be taken at baseline and 4th week. Results will be analysed by using SPSS 24.

02

Conditions studied

  • Runner's Knee

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Keywords

  • pain
  • agility
  • rehabilitation
  • decceleration
  • proprioception training
03

In context

Pain

2,492 studies on the registry are indexed under Pain; 950 are open to participants now.

This study's planned enrollment of 42 is below the median of 70 across 2,140 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

University of Management and Technology Lahore is the lead sponsor of 34 studies on the registry; 19 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 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

  • Athlete with Runner's knee
  • Anterior knee pain (NPSR 4-6) during activities
  • Contact sports
  • Male and Female athletes aged 18-35 years(Raju, Jayaraman et al. 2024)
  • Pain persisting ≥ 3 month
  • Pain on patellar grind test

Exclusion criteria

Exclusion Criteria:

  • Patients with recent lower limb fractures or dislocations
  • history of Knee/hip joint surgery/trauma
  • Signs, symptoms, or radiological findings of intra-articular pathologies, such as effusion, ligamentous or meniscal involvement
  • Referred pain from the hip, back, or sacroiliac joint
  • history of Acute knee strain or sprain
  • Patients on medication such as NSAIDs or corticosteroids
  • diagnosed with Degenerative and infectious arthritis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    McGill Core Stability Exercises

    McGill Big three exercises for 15 repetitions with 15 sec hold, 3 sets for 4 weeks(4/week) McGill curl-up Side plank McGill Bird Dog exercise (Hessam et al.,2023) With Baseline treatment: Hot pack for 10min

    Other: McGill Core stability exercises

  • Experimental
    Proprioception Training

    Proprioception exercises for 12 repetitions, 3 sets for 4 weeks(4/week) Single leg stance - eye open to close progression (Hold 20 sec) 1st two weeks eye open than last two week progress with close eye (Pompeo et al.,2022) Y-Balance test training \_6 reaches per direction (Zhoe et al., 2026) Wobble board balancing \_ 20 sec hold (Ince, B et al.,2023) With Baseline treatment: Hot pack for 10min

    Other: Proprioception Training

Interventions

  • OtherMcGill Core stability exercises

    McGill Big three exercises for 15 repetitions with 15 sec hold, 3 sets for 4 weeks(4/week) McGill curl-up Side plank McGill Bird Dog exercise (Hessam et al.,2023) With Baseline treatment: Hot pack for 10min

  • OtherProprioception Training

    Proprioception exercises for 12 repetitions, 3 sets for 4 weeks(4/week) Single leg stance - eye open to close progression (Hold 20 sec) 1st two weeks eye open than last two week progress with close eye (Pompeo et al.,2022) Y-Balance test training \_6 reaches per direction (Zhoe et al., 2026) Wobble board balancing \_ 20 sec hold (Ince, B et al.,2023) With Baseline treatment: Hot pack for 10min

06

What researchers measure

Primary outcomes

  1. KUJALA

    Anterior knee pain questionnaire (KUJALA) is used to evaluate knee symptoms and functions mainly in patellofemoral joint disorders. It has high reliability (0.83-0.98) and validity (0.90-0.92, consisting of 13 MCQs that shows how knee act in daily activities demonstrating quadriceps strength and hamstrings flexibility. Each question is scored and total score will be between 0-100; more score indicate improved knee function. According to scores, functional outcomes are divided in poor (0-49), fair (50-69), good (70-89) and outstanding (90-100) giving knee joint condition and validating health.

    Time frame: Readings will be taken pre treatment and post treatment.

  2. Star Excursion Test

    This test is used to access dynamic postural control of lower limb, analyze functional deficits in return to play phase and also identify risk of injuries in individuals. During test, individual stand barefoot in middle of eight lines with feet together, then he try to reach maximum distance along each line with distal portion of reaching foot, touch along line and return to keep balance on support. However when individual retake double leg stance after reach, test is over. The measured distance in centimeters demonstrate the dynamic postural performance of the stance limb

    Time frame: Readings will be taken pre treatment and post treatment.

  3. Single leg stance

    A standardized clinical test for evaluating postural stability and static balance is the Single Leg Stance Test (SLST). It assesses a person's capacity to stay balanced when standing on one limb without assistance. The SLST has shown good to exceptional reliability (ICC = 0.75-0.99) across a range of demographics and is simple to administer without the need for specialist equipment. In both clinical practice and research, SLST is regarded as a viable and dependable outcome measure for assessing balance.

    Time frame: Readings will be taken pre treatment and post treatment.

  4. Agility T-test

    One of the most popular field-based tests for evaluating athletes' agility, change-of-direction speed, acceleration, deceleration, and lateral movement skills is the Agility T-test. Across many sports populations, it has shown acceptable validity and good-to-excellent dependability. With Intraclass Correlation Coefficients (ICC) for performance variables ranging from 0.65 to 0.96, a 2026 study employing markerless motion capture found moderate to outstanding test-retest reliability. The authors came to the conclusion that the Agility T-test is a trustworthy technique for evaluating biomechanical traits and agility performance throughout several testing sessions

    Time frame: Readings will be taken pre treatment and post treatment.

  5. Functional Hop Test

    A popular performance-based evaluation for lower-limb function, neuromuscular control, dynamic stability, and preparedness for return to sport after lower-extremity injuries, especially anterior cruciate ligament (ACL) surgery, is the Functional Hop Test. It has demonstrated strong construct validity and criterion validity. It effectively differentiates between injured and healthy limbs and correlates with lower-limb muscle strength, dynamic balance, and functional performance.

    Time frame: Readings will be taken pre treatment and post treatment.

07

Study locations

1 site
08

References and documents

Publications

  • Yilmaz O, Soylu Y, Erkmen N, Kaplan T, Batalik L. Effects of proprioceptive training on sports performance: a systematic review. BMC Sports Sci Med Rehabil. 2024 Jul 4;16(1):149. doi: 10.1186/s13102-024-00936-z. PubMed 38965588 ↗

Individual participant data

Plan to share: Yes — The results data collected , de-identified individual participant data will be shared.

Time frame: 6 months after the publication of the manuscript

Access criteria: The data can be requested from the corresponding author.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2026; primary completion for Nov 2026, 0 months later.

Of 1,285 non-industry interventional studies with no phase under Pain, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 28. This study's planned 0 months is below that.

Counting every sponsor, half of 1,308 studies reached it within 11 months; a quarter within 5 and three quarters within 29.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 26, 2026
First posted
Nov 2, 2026
StartEst.
Nov 2, 2026
Primary completionEst.
Nov 2, 2026
CompletionEst.
Dec 25, 2026
Last update
Nov 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07909694
Lead sponsor
University of Management and Technology Lahore
Responsible party
Sponsor
First posted
Nov 2, 2026
Start date
Nov 2, 2026 (estimated)
Primary completion
Nov 2, 2026 (estimated)
Completion
Dec 25, 2026 (estimated)
Last update
Nov 2, 2026

Study contacts

Saba Riaz, MS-OMPT
Contact
sabariaz@umt.edu.pk
92 3477510093
Iqra Shahid, MSPT
principal investigator · University of management and technology

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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