NCT06197958

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 20, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

December 26, 2023

Completed
14 days until next milestone

First Posted

Study publicly available on registry

January 9, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 20, 2024

Completed
Last Updated

January 9, 2024

Status Verified

December 1, 2023

Enrollment Period

4 months

First QC Date

December 26, 2023

Last Update Submit

December 26, 2023

Conditions

Keywords

concentric excerciseeccentric excerciseIliotibial Band

Outcome Measures

Primary Outcomes (3)

  • patellofemoral pain

    pain is measured by VAS (Visual Analogue Scale)

    pre and 6 weeks post interventional

  • range of motion

    ROM is measured by goniometer

    pre and 6 weeks post interventional

  • knee extensor/flexor strength

    knee extensor/flexor strength is measured by knee resisted test and MMT grading

    pre and 6 weeks post interventional

Study Arms (2)

eccentric exercises

EXPERIMENTAL

Group A: Group A will receive 3 sets of eccentric exercises with 10 RM (repetition maximum) in six sessions.

Other: eccentric exercises

concentric exercises

EXPERIMENTAL

Group B: Group B will receive 3 sets of concentric exercises with 10 RM in six sessions

Other: concentric exercises

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.

eccentric exercises

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.

concentric exercises

Eligibility Criteria

Age18 Years - 36 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

barki advance physiotherapy center Multan

Multan Khurd, Punjab Province, 60000, Pakistan

RECRUITING

Related Publications (4)

  • Crossley KM, Stefanik JJ, Selfe J, Collins NJ, Davis IS, Powers CM, McConnell J, Vicenzino B, Bazett-Jones DM, Esculier JF, Morrissey D, Callaghan MJ. 2016 Patellofemoral pain consensus statement from the 4th International Patellofemoral Pain Research Retreat, Manchester. Part 1: Terminology, definitions, clinical examination, natural history, patellofemoral osteoarthritis and patient-reported outcome measures. Br J Sports Med. 2016 Jul;50(14):839-43. doi: 10.1136/bjsports-2016-096384. Epub 2016 Jun 24. No abstract available.

    PMID: 27343241BACKGROUND
  • Glaviano NR, Kew M, Hart JM, Saliba S. DEMOGRAPHIC AND EPIDEMIOLOGICAL TRENDS IN PATELLOFEMORAL PAIN. Int J Sports Phys Ther. 2015 Jun;10(3):281-90.

    PMID: 26075143BACKGROUND
  • Petersen W, Ellermann A, Gosele-Koppenburg A, Best R, Rembitzki IV, Bruggemann GP, Liebau C. Patellofemoral pain syndrome. Knee Surg Sports Traumatol Arthrosc. 2014 Oct;22(10):2264-74. doi: 10.1007/s00167-013-2759-6. Epub 2013 Nov 13.

    PMID: 24221245BACKGROUND
  • Smith BE, Selfe J, Thacker D, Hendrick P, Bateman M, Moffatt F, Rathleff MS, Smith TO, Logan P. Incidence and prevalence of patellofemoral pain: A systematic review and meta-analysis. PLoS One. 2018 Jan 11;13(1):e0190892. doi: 10.1371/journal.pone.0190892. eCollection 2018.

MeSH Terms

Conditions

Patellofemoral Pain Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Study Officials

  • moiz kamal, DPT

    study principal investigator

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
the assessor who will take the readings is blind
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: randomized clinical trail
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 26, 2023

First Posted

January 9, 2024

Study Start

October 20, 2023

Primary Completion

February 20, 2024

Study Completion

February 20, 2024

Last Updated

January 9, 2024

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations