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Clinical Trials/NCT06009822
NCT06009822RecruitingNot Applicable

Investigation of Kinesiophobia and Functional Status of Patients After MPFL Reconstruction

Gazi University1 site in 1 country30 target enrollmentStarted: August 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
Kinesiophobia

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Kinesiophobia

Time Frame: 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 Outcomes

  • Knee Score(up to 3 months)
  • Patellofemoral Knee Score(up to 3 months)
  • Single-leg hop test(up to 3 months)
  • Dynamic balance(up to 3 months)
  • Static balance(up to 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

İnci Hazal Ayas

Research asistant (PT)

Gazi University

Study Sites (1)

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