- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07306455
Validity of Wearable Sensor for Jump Height (Jump)
Evaluatıon of the Valıdıty of a Wearable Motıon Analysıs Sensor in Assessıng Jump Heıght
Study Overview
Status
Intervention / Treatment
Detailed Description
Vertical jump height is widely used as an indicator of lower limb strength and functional performance. Force platforms are the gold standard for jump height measurement but are expensive and not always practical. Wearable motion sensors and smartphone applications have been developed as low-cost and portable alternatives.
This observational study is designed to examine the concurrent validity of the BTS G-sensor, a wearable inertial measurement unit, for measuring countermovement jump (CMJ) height. Measurements obtained from the BTS G-sensor will be compared with those from the My Jump smartphone application, a validated reference tool.
Healthy female volunteers aged 18-35 years will perform countermovement jumps after a standardized warm-up. Each participant's jump height will be simultaneously recorded by both methods. Data will be analyzed using correlation and agreement analyses to determine the level of consistency between the two methods.
This is an observational validation study. Both the BTS G-sensor and the My Jump application were used simultaneously for measurement purposes only. No interventional procedure or assignment was applied to participants.
Clarification on Study Type:
This is an observational validation study. Both the BTS G-sensor and the My Jump smartphone application were used simultaneously for measurement purposes only. No participant assignment or interventional procedure was applied.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Ankara, Turkey (Türkiye), 06520
- Yuksek Ihtisas University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
- Inclusion Criteria:Female volunteers aged 18-35 years
- No history of orthopedic injury in the past 6 months
- No neurological disorders
- Not taking medications affecting balance
- Exclusion Criteria: Body Mass Index (BMI) > 25
- History of orthopedic surgery
- Impaired lower extremity joint range of motion
- Inability to complete the test protocol
- Measurement errors or missing data
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Volunteers
Healthy female participants aged 18-35 years performed countermovement jumps.
Jump height was measured simultaneously using the BTS G-sensor and the My Jump application.
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A wearable motion analysis sensor used to assess countermovement jump height.
Other Names:
A wearable inertial measurement unit (IMU) used to assess countermovement jump (CMJ) height.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Jump Height Measured with BTS G-sensor Compared to My Jump Application
Time Frame: single testing session, Day 1
|
Countermovement jump (CMJ) height measured simultaneously with the BTS G-sensor and the My Jump smartphone application.
Agreement between the two methods will be analyzed using correlation and Bland-Altman plots.
|
single testing session, Day 1
|
|
Jump Height measured with BTS G-sensor compared to My Jump application
Time Frame: single testing session, Day 1
|
The countermovement jump (CMJ) height will be measured simultaneously using the BTS G-sensor and the My Jump smartphone application.
Correlation and agreement between the two methods will be assessed.
|
single testing session, Day 1
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- AnkaraYBU-02-1155
- 02-1155 (Other Identifier: Ankara Yıldırım Beyazıt University Faculty of Health Sciences Ethics Committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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