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Patellofemoral Pain SyndromePFPSNCT07664566

Core Stability Exercises Versus Proprioceptive Training on Pain and Function in Patients With Patellofemoral Pain Syndrome

A study testing Core Stability Exercises, Proprioceptive Training and traditional therapy in people with Patellofemoral Pain Syndrome, run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study will be conducted to investigate the effect of core stability exercises versus proprioceptive training in patients with patellofemoral pain syndrome. Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Patellofemoral Pain Syndrome
What is being tested?
Core Stability Exercises, Proprioceptive Training and traditional therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
63 participants
Where
No sites listed yet
Study dates
30 Jun 2026to 20 Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • A confirmed diagnosis of Patellofemoral Pain Syndrome (PFPS) based on clinical and radiographic examination, with no evidence of other knee pathologies, as verified by an orthopaedic physician
  • Presence of unilateral PFPS for a minimum duration of three months, indicating a chronic condition
  • Age between 18 and 40 years, representing the typical symptomatic population affected by PFPS
  • Body Mass Index (BMI) less than 30 kg/m², ensuring exclusion of obesity as a confounding factor.
  • Report of increased anterior knee pain during at least two of the following patellofemoral stress-provoking activities: stair ascent or descent, squatting, kneeling, running, or prolonged sitting
  • A positive patellar grind test (Clarke's sign) confirming involvement of the patellofemoral joint

Who cannot join

  • Presence of chronic pain conditions unrelated to Patellofemoral Pain Syndrome (PFPS) as Rheumatoid arthritis, Chronic neuropathic pain, chronic low back pain and knee and hip osteoarthritis.
  • Pregnancy or history of recent trauma affecting the pelvic or knee region
  • History of corticosteroid injection in the affected knee
  • Presence of ankle arthritis or gouty arthritis, which may alter lower-limb biomechanics
  • History of previous surgical intervention involving the lumbar spine, hip, knee, or foot
  • Presence of lower-limb structural deformities, including pes planus, knee valgus, or knee varus deformities

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

This study will be conducted to investigate the effect of core stability exercises versus proprioceptive training in patients with patellofemoral pain syndrome.

Read the detailed description

Patellofemoral Pain Syndrome (PFPS) is one of the most prevalent musculoskeletal disorders causing anterior knee pain, particularly during activities that increase patellofemoral joint stress such as squatting, stair climbing, running, or prolonged sitting .Core stability exercises play a fundamental role in maintaining the kinetic chain alignment between the trunk, pelvis, and lower limb. Dysfunction of the lumbopelvic-hip complex can lead to compensatory movement patterns, increasing stress on the knee joint. Strengthening the core muscles, particularly the transversus abdominis, multifidus, and gluteal muscles, enhances postural control and optimizes force transmission during dynamic activities. Proprioceptive training, on the other hand, targets sensorimotor control by enhancing afferent feedback and neuromuscular coordination. Individuals with PFPS often present with impaired joint position sense and delayed neuromuscular responses around the knee, which may contribute to joint instability and persistent pain. Proprioceptive exercises, including balance, perturbation, and kinesthetic training, improve joint stability and coordination by stimulating mechanoreceptors and enhancing central processing of sensory input.Therefore, this study will aim to fill an important gap in the current literature by directly comparing the effects of core stabilization exercises and proprioceptive training on pain intensity, pain pressure threshold, quadriceps muscle strength, and proprioceptive acuity of knee, knee joint range of motion and functional ability in patients with PFPS

Being tested
Core Stability Exercises, Proprioceptive Training, traditional therapy
Keywords
Core Stability Exercises, Proprioceptive Training, Patellofemoral Pain Syndrome, Pain and Function
Medical subject headings
Patellofemoral Pain Syndrome, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Core Stability ExercisesOther

    core stability exercises including warm-up, main training, and cool-down phases; warm up exercises in the form of Cat-Camel exercise will be performed for 5-8 cycles to mobilize the spine and promote smooth segmental motion. The primary main training consisted of McGill's "Big Three" core stabilization exercises, which emphasize endurance and control of the deep stabilizing muscles, curl up, side bridge, and Quadrupedal stance, finallly the cool down phase had dynamic stretching at the end of each session to reduce muscle tension and promote recovery plus tradional therapy

  • Proprioceptive TrainingOther

    proprioceptive training consisted of group of exercises for balance on 1 leg on a stable surface and a unstable surface. in addition to tradional therapy.

  • traditional therapyOther

    tradional therapy in the form of interferential therapy, knee strengthening exercises, knee strengthening exercises, stretching exercises, patellar mobilization and ischemic compression

Study groups in NCT07664566
Study groupRoleWhat they receive
Core Stability ExercisesExperimentaltwenty one patients with patellofemoral pain syndrome will receive Core stability exercises + traditional physical therapy three times a week for four weeks.
Receives: Other: Core Stability Exercises; Other: traditional therapy
Proprioceptive TrainingExperimentalTwenty-one patients with patellofemoral pain syndrome will receive proprioceptive exercises + traditional physical therapy three times a week for four weeks.
Receives: Other: Proprioceptive Training; Other: traditional therapy
traditional therapyActive comparatortwenty one patients with patellofemoral pain syndrome will receive traditional physical therapy three times a week for four weeks.
Receives: Other: traditional therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. pain intensity

    pain will be assessed by VAS which line on a 100 mm , where 0 indicates no pain and 100 indicates the worst possible pain.

    Measured: up to four weeks

  2. knee disability

    knee disability will be assessed by Kujala Patellofemoral Questionnaire.Which is a 13-item questionnaire including different items on pain related to functioning and activities. The categories within each item are weighted and item scores summed to provide an overall index scored from 0 to 100, where the maximum score of 100 represents no disability.

    Measured: up to four weeks

Secondary outcomes (4)
  1. pressure pain threshold

    The pressure algometer will be used to assess pressure pain threshold

    Measured: up to four weeks

  2. knee range of motion

    The electro goniometer will be used to assess knee range of motion.

    Measured: up to four weeks

  3. knee proprioception (joint position error)

    proprioception will beassesseds by electrogoniometer. The participant's knee will be passively positioned at a target angle (e.g., 30° flexion) then returned to the starting position, then the patient will be asked to actively reproduce the target angle.The absolute angular error (degrees) between the target and reproduced angles will be recorded.

    Measured: up to four weeks

  4. quadriceps muscle strength

    Quadriceps muscle strength will be measured by a handheld dynamometer.

    Measured: up to four weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2026
  2. Study start30 Jun 2026 (estimated)
  3. Primary completion20 Mar 2027 (estimated)
  4. Study completion20 Mar 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Core Stability Exercises and Proprioceptive Training
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
63 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07664566
Sponsor's protocol ID
P.T.REC/012/006411
Acronym
PFPS
Status last verified
Jun 2026
First submitted
18 Jun 2026
Last updated
24 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Core Stability Exercises, Proprioceptive Training and traditional therapy in people with Patellofemoral Pain Syndrome, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact mohamed hassan, phd (0 11 21363081, mohamed.hassan.salama7@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

pain intensity (time frame: up to four weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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