Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID07089628

Investigation of the Relationship Between Core Stability and Reaction Time, Hand-Eye Coordination, Pain, and Functional Status in Individuals With Rotator Cuff Lesions

Led by Bandırma Onyedi Eylül University · Updated on 2025-09-18

52

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

B

Bandırma Onyedi Eylül University

Lead Sponsor

G

Gazi University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Rotator cuff lesions are common musculoskeletal problems that often cause pain, reduce function, and lower quality of life, especially as people age due to degenerative changes in tendon structure. Researchers are exploring how core stability, which supports the spine and improves joint strength and endurance, relates to reaction time and hand-eye coordination in people with these lesions. This study aims to compare these factors between individuals with rotator cuff lesions and those without shoulder problems. Participants are divided into two groups: one with rotator cuff lesions and a control group of asymptomatic individuals matched by age, sex, and education. There is no treatment given; instead, participants undergo various assessments to measure core stability, reaction time, hand-eye coordination, pain, and functional status. These assessments include tests like the modified "Biering-Sorensen" test, trunk flexors endurance test, lateral bridge test, prone bridge test, modified push-ups, sit-ups, reaction time tests, Hand-Wall Toss Test, Visual Analogue Scale for pain, and the Shoulder Pain and Disability Index. During the study, participants complete all these tests at baseline to evaluate their physical abilities and symptoms. The research team collects data on core endurance and motor function to understand how rotator cuff lesions may affect these areas. The study includes adults aged 18 to 65 years, and the total participation involves the completion of these assessments without any intervention or treatment. The findings will help clarify the relationship between core stability and motor functions in affected individuals compared to healthy controls.

CONDITIONS

Brief Title

Investigation of the Relationship Between Core Stability and Reaction Time, Hand-Eye Coordination, Pain, and Functional Status in Individuals With Rotator Cuff Lesions

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Having a diagnosis of a rotator cuff lesion confirmed by a physician
  • Having no history of any surgical procedure related to the shoulder
  • Experiencing activity-related pain scored as 3 or higher on the Visual Analog Scale
  • Age between 18 and 65 years
  • Both males and females can participate
Not Eligible

You will not qualify if you...

  • Presence of systemic inflammatory diseases
  • Pregnancy
  • Presence of mental health disorders
  • Individuals with communication difficulties
  • Having other significant shoulder pathologies such as dislocation, fracture, arthritis, or frozen shoulder
  • History of shoulder surgery
  • Age under 18 or over 65 years old
  • Any conditions that prevent participation in physical assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo baseline assessments to evaluate core stability, reaction time, hand-eye coordination, pain, and functional status.

1 visit (in-person)

Long-term Monitoring

Duration - Up to study completion

Participants are observed without intervention to monitor their condition over time.

No scheduled visits

Trial Site Locations

Total: 1 location

1

Gazi University

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

Eren Özen

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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