Investigation of Kinesiophobia and Functional Status of Patients After MPFL Reconstruction

Sponsor
Gazi University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06009822
Collaborator
(none)
30
1
2
15

Study Details

Study Description

Brief Summary

Our aim in this study is to examine the functional and clinical results of patients who have undergone MPFL reconstruction at least 2 years after the operation. The presence of kinesiophobia of the patients will be evaluated and its relationship with functional outcomes will be examined.

Condition or Disease Intervention/Treatment Phase
  • Other: Postoperative outcome measurements

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Investigation of Kinesiophobia and Functional Status of Patients After MPFL Reconstruction
Actual Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Patients with Medial Patellofemoral Ligament reconstruction

Must have undergone unilateral medial patellofemoral ligament (MPFL) reconstruction. At least 2 years post MPFL reconstruction surgery. Absence of patellar instability subsequent to the surgical procedure. Exclusion of patients with any orthopedic or neurological issues that might impact functionality, except for those who have undergone unilateral MPFL reconstruction.

Other: Postoperative outcome measurements
Kinesiophobia; It will be assessed on the Tampa Kinesiophobia Scale. Function; Lysholm knee score, kujala knee score, single-leg hop test, Y balance test and single leg sway index will be evaluated. Biodex Bio-balance system device will be used for single leg sway index.

Outcome Measures

Primary Outcome Measures

  1. Kinesiophobia [up to 3 months]

    Kinesiophobia refers to an excessive, irrational fear of movement or physical activity. The Tampa Scale for Kinesiophobia was used for assessment. The Tampa Scale for Kinesiophobia is scored between 17-68. A high score indicates high kinesiophobia.

Secondary Outcome Measures

  1. Knee Score [up to 3 months]

    Function will be measured by the Lysholm knee score.The total score on the Lysholm Knee Score questionnaire can range from 0 to 100, with higher scores indicating better knee function and less impairment. General breakdown of the score interpretation: 95-100: Excellent knee function 84-94: Good knee function 65-83: Fair knee function Below 65: Poor knee function

  2. Patellofemoral Knee Score [up to 3 months]

    Function will be measured by the Kujala Patellofemoral Knee Score. The total score on the Kujala Patellofemoral Knee Score questionnaire can range from 0 to 100, with higher scores indicating better knee function and less impairment. General breakdown of the score interpretation: 100: No limitations or symptoms 85-99: Mild limitations or symptoms 70-84: Moderate limitations or symptoms Below 70: Severe limitations or symptoms

  3. Single-leg hop test [up to 3 months]

    The single-leg hop distance is an indicator of lower extremity function. The test evaluates an individual's lower limb strength, power, and overall functional performance. It specifically focuses on assessing an individual's ability to generate power and stability while performing a single-leg hop for maximal distance. When performing the test, the individual starts by standing on one leg at the starting point. The opposite leg is lifted slightly off the ground, and the hands can be placed on the hips or kept at the sides for balance. On the command to start, the individual hops forward on the single leg, aiming to jump as far as possible while maintaining control and balance. Perform 3 repetitions and record the longest distance jumped.

  4. Dynamic balance [up to 3 months]

    Dynamic balance will be measured by Y Balance Test. The Y Balance Test involves a person standing on one leg while reaching in anterior (forward), posteromedial (backward and to the side), and posterolateral (backward and to the other side) directions with the other leg. The person places their stance foot at the starting point on the central part of the Y-shaped device.While maintaining balance on the stance leg, the person reaches the free leg as far as possible along each of the three arms of the Y.The distance reached in each direction is measured and recorded.

  5. Static balance [up to 3 months]

    Static balance will be measured using a Biodex Balance System, single leg sway index test procedure. The device reports the person's body oscillations as sway index. A high stability index indicates poor postural control.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Undergone unilateral medial patellofemoral ligament (MPFL) reconstruction

  • At least 2 years after the operation

Exclusion Criteria:
  • Patellar instability

  • Knee ligament injury

  • Meniscus injury

  • Knee osteoarthritis

  • Ankle ligament injury

  • Ankle osteoarthritis

  • Any neurological disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gazi University Ankara Turkey

Sponsors and Collaborators

  • Gazi University

Investigators

  • Study Director: Zeynep Hazar, Gazi University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
İnci Hazal Ayas, Research asistant (PT), Gazi University
ClinicalTrials.gov Identifier:
NCT06009822
Other Study ID Numbers:
  • Iayas4
First Posted:
Aug 24, 2023
Last Update Posted:
Aug 24, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2023