NCT07111923

Brief Summary

This study employed a single-group repeated measures design, conducted in accordance with the STROBE reporting guidelines. Nineteen participants who met the inclusion criteria were recruited. All assessments were performed individually in a quiet, controlled environment to minimize external distractions. Participants were instructed to avoid intense physical activity, caffeine consumption, and to wear appropriate sports attire for at least 48 hours prior to testing. Upon arrival, participants rested in a seated position while demographic data were collected. Each test procedure was explained both verbally and visually, and participants were allowed to perform a practice trial to ensure comprehension. A crossover design was used to counterbalance the order of conditions (hands on hips vs. hands free), which was randomly assigned. Repeated measurements were conducted 24 hours after the initial assessments, at the same time of day, to control for diurnal variation. Detailed descriptions of the tests performed are provided in the following sections.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
19

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 2, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 2, 2024

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 7, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 28, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

August 8, 2025

Completed
Last Updated

August 8, 2025

Status Verified

August 1, 2025

Enrollment Period

1 year

First QC Date

July 28, 2025

Last Update Submit

August 1, 2025

Conditions

Keywords

AthleteBalanceHand positionReactive

Outcome Measures

Primary Outcomes (2)

  • Y Balance Test

    The Y Balance Test (YBT) is a shortened version of the Star Excursion Balance Test. It assesses reach distances in three directions: anterior, posteromedial, and posterolateral

    through study completion, an average of 1 year

  • Reactive Balance Test

    The Reactive Balance Test (RBT) incorporates the YBT setup with an LED light system connected to a smartphone application. For RBT, LED lights were placed at 80% of the participants' maximum reach distance in the anterior, posteromedial, and posterolateral directions of the YBT setup (ReactionX).

    through study completion, an average of 1 year

Secondary Outcomes (1)

  • Lower Extremity Length

    through study completion, an average of 1 year

Study Arms (1)

Balance Assessment Group

EXPERIMENTAL
Other: Balance Assesment

Interventions

The study design was a single-group repeated measures design. Nineteen individuals meeting the inclusion criteria were included. The assessments were conducted individually in a quiet environment, isolated from other athletes and external factors. Athletes were instructed to refrain from intense exercise and training, avoid caffeine consumption, and attend the assessment in sportswear within the last 24 hours. Upon arrival for the assessments, athletes were seated to rest while demographic information was collected. Each test was explained verbally and visually, and participants were allowed to perform a trial. A crossover design method was used in the study, with the order of tests (hands on hips or hands free) determined randomly. Retest measurements were conducted 24 hours after the initial test at the same time of day. The tests performed are described below.

Balance Assessment Group

Eligibility Criteria

Age10 Years - 18 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Voluntary participation
  • Female
  • Volleyball player
  • Age 10-18

You may not qualify if:

  • Color blindness
  • Attention deficit disorder
  • Orthopedic or neurological diagnosed disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Balikesir University

Balıkesir, Bigadiç, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

July 28, 2025

First Posted

August 8, 2025

Study Start

November 2, 2023

Primary Completion

November 2, 2024

Study Completion

June 7, 2025

Last Updated

August 8, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations