Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
29 participants
OBSERVATIONAL
2025-03-01
2025-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
BTS G-sensor
A wearable motion analysis sensor used to assess countermovement jump height.
BTS G-sensor
A wearable inertial measurement unit (IMU) used to assess countermovement jump (CMJ) height.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
BTS G-sensor
A wearable motion analysis sensor used to assess countermovement jump height.
BTS G-sensor
A wearable inertial measurement unit (IMU) used to assess countermovement jump (CMJ) height.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No neurological disorders
* Not taking medications affecting balance
Exclusion Criteria
* Impaired lower extremity joint range of motion
* Inability to complete the test protocol
* Measurement errors or missing data
18 Years
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Busra Kalkan Balak
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Busra Kalkan Balak
Principal Investigator, PT, PhD
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Yuksek İhtisas University
Ankara, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Ankara Yildirim Beyazıt University Faculty of Health Sciences
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
02-1155
Identifier Type: OTHER
Identifier Source: secondary_id
AnkaraYBU-02-1155
Identifier Type: -
Identifier Source: org_study_id