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Comparison of Concentric-eccentric Exercises in Patellofemoral Pain Syndrome

Comparison of Concentric-eccentric Exercises in Patellofemoral Pain Syndrome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06197958
Enrollment
24
Registered
2024-01-09
Start date
2023-10-20
Completion date
2024-02-20
Last updated
2024-01-09

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

Conditions

Patello Femoral Syndrome, Patellofemoral Pain, Knee Pain Chronic

Keywords

concentric excercise, eccentric excercise, Iliotibial Band

Brief summary

Patellofemoral pain syndrome is due to dysfunctional dynamic knee valgus resulting from decrease in strength of hip abductors or abnormal rear-foot eversion with pes pronatus valgus. It is also associated with vastus medialis/vastus lateralis disbalance, hamstring tightness or iliotibial tract tightness.

Detailed description

Patellofemoral pain syndrome is due to dysfunctional dynamic knee valgus resulting from decrease in strength of hip abductors or abnormal rear-foot eversion with pes pronatus valgus. It is also associated with vastus medialis/vastus lateralis disbalance, hamstring tightness or iliotibial tract tightness. The pain is felt around or behind the patella. The causes are multifactorial. A decline in ability to perform physical activity is seen. The aim of this study will be to compare the effects of concentric and eccentric exercises on pain, strength and ROM in patellofemoral pain syndrome.A randomized clinical trial will be performed at Barki Advance Physiotherapy Center Multan through convenience sampling technique on 24 patients which will be allocated through random sampling through sealed opaque enveloped into group A and group B. Group A will receive eccentric exercises like walking down stairs, lowering a weight during shoulder press, the downward motion of squatting, the downward motion of a push-up, lowering the body during a crunch, lowering the body during a pull-up 3 sets with 10 RM (repetition maximum) for six week training. The group B will receive concentric exercises like walking upstairs, pushing up in a bench press, the beginning portion of a deadlift when you lift the barbell off the ground, sitting up in a sit up, pushing up from a lowered push-up and standing up in a back squat 3 sets with 10 RM. Screening tools include patellar grind test with positive Clark's sign and VAS (visual analogue scale) for pain rating. Outcomes will be measured through knee resisted test and MMT grading for knee extensor/flexor strength and goniometer for ROM. Data will be analyzed using SPSS software version 25. After assessing normality, it will be decided either parametric or non parametric test will be used within a group or between two groups. Effectiveness of concentric and eccentric exercises will be analyzed by comparison in individuals with patellofemoral pain syndrome.

Interventions

eccentric exercises like walking down stairs, lowering a weight during shoulder press, the downward motion of squatting, the downward motion of a push-up, lowering the body during a crunch, lowering the body during a pull-up 3 sets with 10 RM (repetition maximum) for six week training.

concentric exercises like walking upstairs, pushing up in a bench press, the beginning portion of a deadlift when you lift the barbell off the ground, sitting up in a sit up, pushing up from a lowered push-up and standing up in a back squat 3 sets with 10 RM.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

the assessor who will take the readings is blind

Intervention model description

randomized clinical trail

Eligibility

Sex/Gender
ALL
Age
18 Years to 36 Years
Healthy volunteers
Yes

Inclusion criteria

* Players between the age 18 to 36 years. * Both male and female gender. * Patients who have Patellar grind test positive. * The presence of retropatellar or peripatellar pain. * Reproduction of retropatellar or peripatellar pain with squatting, stair climbing, prolonged sitting, or other functional activities loading the PFJ in a flexed position.

Exclusion criteria

* Individuals with a history of recent trauma or surgery of lower limb (16), administration of steroid injection in the past 6 months. * Recent administration of platelet-rich plasma containing growth factors, diagnosis of rheumatoid arthritis, myositis ossificans, diagnosis of other muscular disorder. * Patients who had taken physical therapy of any sort in the past six months will be excluded from the study. * Furthermore, individuals with any history of occupation-related pain will be ruled out

Design outcomes

Primary

MeasureTime frameDescription
patellofemoral painpre and 6 weeks post interventionalpain is measured by VAS (Visual Analogue Scale)
range of motionpre and 6 weeks post interventionalROM is measured by goniometer
knee extensor/flexor strengthpre and 6 weeks post interventionalknee extensor/flexor strength is measured by knee resisted test and MMT grading

Countries

Pakistan

Contacts

Primary ContactAmna Shahid, MS-DPT
amna.shahid@riphah.edu.pk+92 334 4512823

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026