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

NCT07574788 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2026-05-13

No results posted yet for this study

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 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.

Conditions

  • Reaction Time
  • Proprioception
  • Power
  • Performance
  • Athletic Performance
  • Flexi-bar

Interventions

OTHER

flex-i bar

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

OTHER

Theraband Flex-Bar

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

OTHER

Rolling-pin

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

Sponsors & Collaborators

  • Aydın Adnan Menderes University Scientific Research Projects Unit

    collaborator UNKNOWN

  • Aydin Adnan Menderes University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-05-01
Primary Completion
2026-08-01
Completion
2026-08-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07574788 on ClinicalTrials.gov