The Effect of Hand Position on Balance
1 other identifier
interventional
19
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2023
1 active site
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
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 2, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 7, 2025
CompletedFirst Submitted
Initial submission to the registry
July 28, 2025
CompletedFirst Posted
Study publicly available on registry
August 8, 2025
CompletedAugust 8, 2025
August 1, 2025
1 year
July 28, 2025
August 1, 2025
Conditions
Keywords
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
EXPERIMENTALInterventions
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.
Eligibility Criteria
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)
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