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Pilates-based Core Strengthening on Patellofemoral Pain Syndrome

Incorporation of Pilates-based Core Strengthening Exercises Into the Rehabilitation Protocol for Adolescents With Patellofemoral Pain Syndrome: a Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05120583
Acronym
Pilates
Enrollment
34
Registered
2021-11-15
Start date
2020-11-01
Completion date
2021-10-30
Last updated
2021-11-22

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

Conditions

Patellofemoral Pain Syndrome

Keywords

patellofemoral pain syndrome, Pilates exercises, functional status

Brief summary

Patellofemoral pain syndrome (PFPS) is one of the most common musculoskeletal pain conditions that tend to become a chronic problem. PFPS is common among young adolescents, particularly in physically active individuals aged 12 to 17 years old with more prevalence among females, as it affects females 1.5 - 3 times when compared to males.

Detailed description

Adolescents with PFPS usually complain of retro-patellar pain (behind the kneecap) or peripatellar pain (around the kneecap) and crepitation in the knee joint, and also there is discomfort while sitting with a flexed knee for a long time. Symptoms are usually exacerbated by activities that increase the load on patellofemoral joints such as weight-bearing activities, squatting, walking up or downstairs, and running. PFPS takes place whenever the muscles around the knee fail to keep the kneecap properly aligned, leading to abnormal lateral tracking of the patella.Overuse such as running and jumping sports, the trauma of kneecaps such as fracture, dislocation, or knee surgery may also predispose to PFPS.

Interventions

OTHERPilates exercises

Side kick internal/ external rotation with Pilate's band

OTHERTraditional physical therapy program

strength, flexibility

Sponsors

Cairo University
CollaboratorOTHER
Prince Sattam Bin Abdulaziz University
CollaboratorOTHER
Qassim University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
14 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Pain felt anterior to knee joint. * Pain felt retro-patellar. * Pain felt during rest and increased with activities like prolonged sitting, squatting, running, and stair climbing. * Insidious onset lasting for more than 6 weeks. * Without any traumatic incidence. * Not participating in a physical therapy program for the past three months.

Exclusion criteria

* If they had a meniscal tear. * Cruciate/collateral ligaments involvement. * Knee osteoarthritis. * Rheumatoid arthritis. * A history of knee or hip surgery. * Patellar dislocation/subluxation. * Traction apophysitis encompassing the patellofemoral complex. * Any pathology in the patellar tendon. * Spinal referred pain.

Design outcomes

Primary

MeasureTime frameDescription
Pain assessmentat baselineassessed by using a visual analog scale, 10-cm VAS scale, with 0 indicating no pain and 10 for worst pain sensation
Muscle strength assessmentat baselineassessed using a calibrated handheld dynamometer

Secondary

MeasureTime frameDescription
Functional statusat baselineevaluated using the Arabic version of the Anterior Knee pain Questionnaire, The score ranges from 0 to 100, with 0 indicating complete functional limitation and 100 indicating no pain and no functional limitation.
health-related quality of lifeat baselineassessed by using the self-report Pediatric Quality of Life Inventory, it includes 23 items distributed among 4 domains \[physical (8 items), emotional (5 items), social (5 items), and school functions (3 items)\]. Each item is rated on a 5- points scale (0 means never, and 4 means almost always). Items are transformed linearly to 0-100 scale (0 = 100, 1 = 75, 2 = 50, 3 = 25, and 4 = 0).

Countries

Saudi Arabia

Outcome results

None listed

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