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MUSCLE STRENGTH IMBALANCE AND KINESIOPHOBIA IN MENISCUS PATIENTS

EVALUATION OF THE RELATIONSHIP BETWEEN MUSCLE STRENGTH IMBALANCE AND KINESIOPHOBIA IN POSTOPERATIVE AND CONSERVATIVELY MANAGED MENISCUS PATIENTS

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07407075
Enrollment
46
Registered
2026-02-12
Start date
2026-02-06
Completion date
2026-03-09
Last updated
2026-03-16

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

Conditions

Kinesiophobia, Meniscus Injury, Muscle Strength

Keywords

Meniscus Injuries, Kinesiophobia, BlazePod, Pain

Brief summary

This study is a cross-sectional and comparative clinical investigation designed to examine the relationship between periarticular muscle strength imbalance and kinesiophobia levels in individuals with meniscal injuries receiving postoperative or conservative treatment, and to determine whether this relationship differs according to the treatment modality.

Interventions

None listed

Sponsors

Acıbadem Atunizade Hospital
Lead SponsorOTHER
Biruni University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Being between 18 and 50 years of age, with a diagnosis of meniscal injury (male or female) * Having a medial meniscal injury confirmed by magnetic resonance imaging (MRI) * Presence of a unilateral injury * Voluntary agreement to participate in the study * A minimum of 3 weeks having elapsed since surgery for postoperative participants * A minimum of 2 months having elapsed since injury for participants receiving conservative treatment

Exclusion criteria

* Concomitant anterior cruciate ligament (ACL) injury or additional ligament injuries such as posterior cruciate ligament (PCL), lateral collateral ligament (LCL), or medial collateral ligament (MCL) * History of fracture or significant trauma to the lower extremity within the past 6 months * Current or previous neurological disorders (e.g., stroke, multiple sclerosis, peripheral neuropathy, Parkinson's disease) * Vestibular system disorders or any conditions affecting balance * Presence of a second surgical intervention or postoperative complications * Osteoarthritis with a Kellgren-Lawrence grade ≥ 2 * Contracture or severe limitation of knee range of motion restricting joint mobility

Design outcomes

Primary

MeasureTime frameDescription
Muscle StrengthBaseline. The assessment will be conducted once during the study period.Muscle strength will be assessed using a standardized isometric dynamometer. It will be applied to the quadriceps and hamstring muscles.This will be used to objectively measure isometric muscle strength and determine the difference/asymmetry of strength between the affected and unaffected extremities. This measure quantitatively reflects lower extremity muscle performance and potential functional strength loss.
Tampa Kinesiophobia Scale (TKS-17)Baseline. The evaluation is conducted only once during the research process.This is a self-report scale that assesses avoidance of movement and fear of re-injury. It consists of 17 articles. The scale will be completed using a 4-point Likert scale (1=Strongly disagree, 4=Strongly agree), and the total score will range from 17 to 68.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS)Baseline. The evaluation will be conducted once during the study period.Pain intensity will be assessed using a Visual Analog Scale (VAS) to determine the level of knee pain perceived by participants and will be recorded as a quantitative indicator of subjective pain experience. Pain intensity will be rated on a scale of 0-10. A score of "0" indicates "no pain", and a score of "10" indicates "unbearable pain".
Single Leg Hop TestBaseline. The evaluation will be conducted once during the study period.Functional performance will be assessed using the Single Leg Hop Test, which will provide objective data on the dynamic stability, power generation, and functional capacity of the lower extremity.
International Knee Documentation Committee (IKDC)Baseline, The evaluation will be conducted once during the study period.Participants' knee-related symptoms and functional level will be assessed using the IKDC-SKF. The form consists of items covering symptoms (pain, swelling, locking), activities of daily living, and sports activities, and a score on a scale of 0-100 is obtained; a higher score indicates better function.
Lysholm Knee ScaleBaseline. The evaluation will be conducted once during the study period.The Lysholm score is a scale that evaluates knee function on an eight-item scale, scored from 0-100; scores of 92-100 are interpreted as "excellent", 84-91 as "good", 65-83 as "average", and 64 and below as "poor".
Reaction Time Assessment (BlazePod)Baseline. The evaluation will be conducted once during the study period.In this study, the BlazePod Reaction Measurement System will be used to evaluate the neuromuscular response velocity of the lower extremity. The test will last for 60 seconds, the reaction time for each stimulus will be automatically recorded in milliseconds, and the average reaction time will be used in the analysis. A shorter reaction time indicates a better neuromuscular response speed.
ProprioceptionBaseline. The evaluation will be conducted once during the study period.In this study, the active joint position repetition test will be used to evaluate proprioceptive sensation in the knee joint.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORBegüm KARA KAYA, PhD

Biruni University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026