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Not Yet RecruitingNCT06674083

Reliability of the Gyko Inertial Sensor System in Evaluating Jumping and Postural Stability Parameters in Healthy Adults

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
55 (estimated)
Sponsor
Hacettepe University · Academic / Other
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

The aim of the study is to examine the Gyko inertial sensor system in healthy adults. In the study, jump and postural control parameters are assessed with a one-week interval. To evaluate intra-rater reliability, ICC, SEM, and MDC values will be calculated.

Detailed description

The Gyko inertial sensor system is a lightweight and portable device that applies protocols for assessing and monitoring joint function, muscle strength, jump, and postural stability parameters during the rehabilitation of a specific musculoskeletal region. Previous studies have evaluated the validity of Gyko in assessing vertical jump height in female sub-elite soccer players and its reliability in evaluating postural stability in healthy, non-athletic adults. However, the findings regarding both the validity and reliability of the device have been limited. Our aim in this study is to evaluate the reliability of the Gyko inertial sensor system, an affordable and accessible tool that facilitates the assessment and monitoring of jump and postural stability parameters in healthy adults. If the study confirms the reliability of the Gyko device in evaluating these parameters, it could be used by clinicians, therapists, researchers, and/or coaches as a targeted alternative to gold standard methods for assessing jump and postural stability parameters in healthy adults. Hypotheses: H0: The use of the Gyko inertial sensor system is not reliable for assessing jump and postural control parameters in healthy adults. H1: The use of the Gyko inertial sensor system is reliable for assessing jump performance in healthy adults. H2: The use of the Gyko inertial sensor system is reliable for assessing postural control in healthy adults.

Conditions

Timeline

Start date
2025-02-01
Primary completion
2025-04-01
Completion
2025-05-01
First posted
2024-11-05
Last updated
2024-11-06

Source: ClinicalTrials.gov record NCT06674083. Inclusion in this directory is not an endorsement.