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Completed

NCT Number: NCT07111923

The Effect of Hand Position on Balance

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.

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Key information

Age range

10 year–18 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Balikesir University

Balıkesir, Bigadiç, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Balance Assesment

Other

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.

Primary outcomes

  1. Y Balance Test

    Time frame: through study completion, an average of 1 year

    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

  2. Reactive Balance Test

    Time frame: through study completion, an average of 1 year

    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).

Secondary outcomes

  1. Lower Extremity Length

    Time frame: through study completion, an average of 1 year

    While the athlete was in a supine position on a mat, the distance between the ASIS (anterior superior iliac spine) and the medial malleolus was measured on both the right and left sides using a measuring tape. The lower extremity length was used to calculate the YBT composite score

Sponsors and collaborators

Lead sponsor

Balikesir University

Other

Registry information

Official study title

The Effect of Hand Position on Lower Extremity Y Balance and Reactive Balance Tests: A Cross-Sectional Study

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Aug 8, 2025
Registry last updated
Aug 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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