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Reaction TimeEXBAR-RTNCT07574788

Acute Effects of Exercise Bars on Proprioception, ReactionTime, Power and Upper Extremity Performance

A study testing flex-i bar, Theraband Flex-Bar and Rolling-pin in people with Reaction Time and Proprioception, run by Aydin Adnan Menderes University at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study will be conducted between May and August 2026 at Aydın Adnan Menderes University, Faculty of Health Sciences, with male individuals aged 18-35. For the study, cases will first be divided into 3 groups by computer-assisted randomization.The first group will be the Flex-i bar group, the second group will be… Read more about this study

Who is it for?
Ages 18 to 35 years, men onlyHealthy volunteers can take part
Conditions the study is for
Reaction Time, Proprioception, Power
What is being tested?
flex-i bar, Theraband Flex-Bar and Rolling-pin
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 May 2026to 1 Aug 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Aged between 18 and 35 years
  • Healthy individuals
  • No history of upper extremity injury
  • No neurological disorders
  • Voluntary participation

Who cannot join

  • Presence of any neurological disease
  • History of upper extremity surgery
  • Current musculoskeletal pain or injury
  • Any condition affecting proprioception or reaction time
  • Inability to comply with study procedures

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Beril Demirtaş, graduted student contact

+905417163955

berildmrts@gmail.com

Turkey (Türkiye)1 site
  • Aydın Adnan Menderes Üniversitesi

    Aydin

    Beril Demirtaş, gratuded student, 905417163955, berildmrts@gmail.com

    Gürkan Günaydın, associate professor

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Acutely Applied Exercise Bars on Proprioception, Reaction Time, Power and Upper Extremity Performance

This study will be conducted between May and August 2026 at Aydın Adnan Menderes University, Faculty of Health Sciences, with male individuals aged 18-35. For the study, cases will first be divided into 3 groups by computer-assisted randomization.The first group will be the Flex-i bar group, the second group will be the Theraband Flex bar group, and the third group will be the Sham bar group. Group 1 will perform the exercises with the Flex-i bar, while Group 2 will perform them with the Theraband Flex bar. The control group will perform the exercises with a rolling pin.After group assignment of cases is completed, demographic information such as age, height and weight of the participants will be recorded. Then, pre-exercise assessments of the participants will be conducted. The assessment will include proprioception, reaction time, power and upper extremity performance. Following the initial assessment, each group will perform their exercises with their own exercise material. Measurements will be repeated after the exercises. Measurements will be taken three times during the assessments and the best result will be recorded.

Read the detailed description

This study will be conducted between May and August 2026 at Aydın Adnan Menderes University, Faculty of Health Sciences, with male individuals aged 18-35. For the study, cases will first be divided into 3 groups by computer-assisted randomization.The first group will be the Flex-i bar group, the second group will be the Theraband Flex bar group, and the third group will be the Sham bar group. Group 1 will perform the exercises with the Flex-i bar, while Group 2 will perform them with the Theraband Flex bar. The control group will perform the exercises with a rolling pin.After group assignment of cases is completed, demographic information such as age, height and weight of the participants will be recorded. Then, pre-exercise assessments of the participants will be conducted. The assessment will include proprioception, reaction time, power and upper extremity performance. Following the initial assessment, each group will perform their exercises with their own exercise material. Measurements will be repeated after the exercises. Measurements will be taken three times during the assessments and the best result will be recorded.

Proprioception Measurement (Joint Position Sense): Before starting the test, the content of the test will be explained in detail and a trial will be conducted. For the test, the participant will first be asked to sit in a chair with back support. Then their eyes will be covered with an eye mask. A digital inclinometer will be placed on their wrist with Velcro (Baseline 12-1057 digital inclinometer). The researcher will show the participant the desired degree of movement, and the participant will be asked to do this themselves. Then the test phase will begin, and the individual will be asked to actively reach the target angle. The amount of deviation of the angle reached by the individual will be recorded. This process will be repeated 3 times, and the best value will be used as the analysis value.

Measurement of Reaction Time: The time it takes for a person to give a motor response (e.g., pressing a button, reaching for a light) upon perceiving a visual stimulus will be measured in milliseconds (ms). Simple reaction time tests are performed using complex technical equipment such as infrared lasers, step panels, and motion-based approach models. Portable, wireless light devices such as Blazepod, FitLight Trainer, and Reflexlight are among the current equipment used for reaction time. In this study, the Blazepod reaction time meter will be used. The participant will touch the button on one of four illuminated devices placed on a table, according to the visual stimulus, and turn off the light. The duration of the person pressing the button will be automatically detected by the device and the duration will be recorded.

Upper Extremity Performance Measurement: The Upper Quarter Y Balance Test will be used for performance measurement.

The person assumes a plank position (hands on the ground, feet behind). The supporting arm remains stationary, and the arm being tested is extended in 3 different directions: Medial (inward), superolateral (opposite), and inferolateral (outer diagonal backward).

In each extension, the maximum distance that can be reached with the test arm is measured (cm). 3 repetitions are performed for each direction. The furthest distance (maximum reach) is recorded. The distance reached is normalized according to the upper extremity length.

Power Measurement: Seated Medicine Ball Throw (SMBT); is the most commonly used test. It is used to measure the explosive power of the upper body and arm muscles. The participant sits upright against a wall. They throw a 2-3 kg medicine ball forward from chest height with maximum force. The distance reached is measured (the point of initial contact with the ball). The furthest distance (cm) is recorded.

The Flexi bar is an exercise tool designed by German physiotherapists. It weighs 719 grams and is 1520 mm long. It has a rubber handle in the middle (17.9 cm) and consists of a flexible fiberglass pole with rubber weights at both ends. Due to its elastomer properties and rubber structure, the Flexi-bar is designed to resonate at a frequency of 5 Hz when moving forcefully within the range of motion that needs to be maintained while maintaining physical stability. The desired force to be created in the bar, pulling, and control changes that cause changes in the body or living beings. The working principle is to cause the rubber handle to vibrate at 5 Hz by swinging the bar, and then this vibration is transmitted to the whole body through the arm that is held. For the flex-i bar exercise, the participant will be in a standing position. The movements in different angles and positions will be shown to the participant. Then the flexibar will be given to the participant and they will be asked to hold the exercise bar and swing it correctly in accordance with the desired movements. In flexibar exercises, a 1-minute rest period will be given after each exercise to prevent possible fatigue.

Theraband-Flex Bar is a flexible, durable, and economical exercise equipment made of natural rubber, 30.5 cm long. Its textured surface makes it easy to perform movements and grip. It is available in four colors: Yellow, Red, Green, and Blue. The difficulty levels of the FlexBar vary according to their diameters and colors. It is preferred for increasing grip strength, strengthening the upper extremities, hands, and feet through bending or swinging movements, and effectively providing soft tissue movements. Blue will be preferred for the exercise, and a 1-minute rest period will be given after each exercise.

Rolling pin; a standard size (100cm) rolling pin will be preferred in the control group. 1-minute rest period will be given after each exercise.

Exercises Each exercise will be performed for 30 seconds, followed by a 1-minute rest period.

  1. Swing from side to side with elbow straight
  2. Swing forward and backward with elbow straight
  3. Swing from side to side with elbow bent
  4. Swing forward and backward with elbow bent
  5. Swinging the arm outwards with the elbow straight to the right and left.
  6. Swinging the arm outwards with the elbow straight to the forward and backward.
  7. Swinging the shoulder externally to the right and left.
  8. Swinging the shoulder externally to the forward and backward.
Being tested
flex-i bar, Theraband Flex-Bar, Rolling-pin
Keywords
reaction time, proprioception, power, performance tests, performance, exercise bars, acute effect

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • flex-i barOther

    A single session of oscillatory exercise using a Flexi-Bar applied to the upper extremity.

  • Theraband Flex-BarOther

    A single session of upper extremity exercise using a Theraband Flex-Bar.

  • Rolling-pinOther

    A single session of upper extremity exercise using a rolling pin.

Study groups in NCT07574788
Study groupRoleWhat they receive
A-Flexi barExperimentalFor the flexi-bar exercise, the participant will be in a standing position. The participant will be shown movements in different angles and positions. Then, the participant will be given a flexi-bar and asked to hold the exercise bar and swing it correctly according to the desired movements. In flexi-bar exercises, a 1-minute rest period will be given after each exercise to account for possible fatigue.
Receives: Other: flex-i bar
B-Theraband Flex-BarExperimentalThe participant will be in a standing position. The participant will be shown movements in different angles and positions. They are preferred because they increase grip strength, strengthen the upper extremities, hands and feet with bending or swinging movements, and enable soft tissue movements effectively. Blue color will be preferred for the exercise and a 1-minute rest period will be given after each exercise.
Receives: Other: Theraband Flex-Bar
C-Rolling pinOtherRolling pin; a standard size (100cm) rolling pin will be used in the control group. A 1-minute rest period will be given after each exercise.
Receives: Other: Rolling-pin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proprioception

    Joint position sense will be assessed using an inclinometer.(Baseline 12-1057 digital inclinometer)

    Measured: Immediately before and immediately after a single session intervention (within the same day)

  2. Reaction Time

    Reaction time will be measured using a computerized reaction time test.(Blazepod)

    Measured: Immediately before and immediately after a single session intervention (within the same day)

Secondary outcomes (2)
  1. Power

    Muscle power will be assessed using a Single Arm Medicine Ball Throw Test.

    Measured: Immediately before and immediately after a single session intervention (within the same day)

  2. Upper Extremity Performance

    Upper extremity performance will be evaluated using a functional performance test.(UQ Y-Balance Test)

    Measured: Immediately before and immediately after a single session intervention (within the same day)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 May 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion1 Aug 2026 (estimated)
  4. Study completion1 Aug 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
A single-blind study - The participants in the study group will have separate forms. Participants will not know which group they belong to, but the practitioners will be aware of the groups.
Masking
Single blind
Who is masked
Participant
Enrolment
45 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07574788
Sponsor's protocol ID
ADU-FTR-BD-01
Acronym
EXBAR-RT
Status last verified
May 2026
First submitted
12 Apr 2026
Last updated
13 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Study results will be shared

Publications

  • Pourahmadi, M.R., et al., Reliability and validity of an iPhone® application for the measurement of lumbar spine flexion and extension range of motion. PeerJ, 2016. 4: p. e2355. Mourcou, Q., et al., Mobile phone-based joint angle measurement for functional assessment and rehabilitation of proprioception. BioMed research international, 2015. 2015. de-Oliveira, L. A., Matos, M. V., Fernandes, I. G., Nascimento, D. A., & da Silva- Grigoletto, M. E. (2021). Test-retest reliability of a visual-cognitive technology (BlazePod™) to measure response time. Journal of sports science & medicine, 20(1), 179. van der Leeuw, G., Eggermont, L. H. P., Shi, L., Milberg, W. P., Gross, A. Hausdorff, J. M., ... ve Lipsitz, L. A. (2016). Pain and cognitive function among older adults living in the community. The Journals of Gerontology: Series A, 71(3), 398-405. Ruffe, N. J., Sorce, S. R., Rosenthal, M. D., ve Rauh, M. J. (2019). Lower quarter- and upper quarter Y balance tests as predictors of running-related injuries in high school cross-country runners. International Journal of Sports Physical Therapy, 14(5), 695-706. Wang, D., Gibbons, M., Shung, J., ve Hame, S. (2016). Functional testing and return to sport after ACL reconstruction. Current Reviews in Musculoskeletal Medicine, 9(3), 330-336. Mischi, M., & Cardinale, M. (2009). The effects of a 28-Hz vibration on arm muscle activity during isometric exercise. Medicine & Science in Sports & Exercise, 41(3), 645-653 Escamilla, R.F., et al., An electromyographic analysis of the shoulder complex musculature while performing exercises using the bodyblade® classic and bodyblade® pro. International Journal of Sports Physical Therapy, 2016. 11(2): p. 175. de Lima Boarati, E., et al., Acute effect of flexible bar exercise on scapulothoracic muscles activation, on isometric shoulder abduction force and proprioception of the shoulder of individuals with and without subacromial pain syndrome.Clinical Biomechanics, 2020.

Questions about this trial

What is this clinical trial studying?

A study testing flex-i bar, Theraband Flex-Bar and Rolling-pin in people with Reaction Time and Proprioception, run by Aydin Adnan Menderes University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 13 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Beril Demirtaş, graduted student (+905417163955, berildmrts@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proprioception (time frame: Immediately before and immediately after a single session intervention (within the same day)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07574788, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 May 2026.

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