The Effect of Different Sensory Conditions on Sensory Interaction in Balance

Bezmialem Vakif University

Status: Completed

Conditions: Sensory Science; Balance Assessment

Study type: Observational

Funder types: Other

Identifiers

NCT06756997

E-54022451-050.04-173777

Details and patient eligibility

About

The ability of humans to maintain spatial orientation and balance control relies on accurate and complete sensory information. This study aims to investigate the effects of different sensory conditions on the sway index (balance). Adults with normal hearing, vision, and balance abilities will perform the Modified Clinical Test of Sensory Interaction on Balance (mCTSIB), a test from the Biodex Balance System, under varying sensory conditions. The first sensory condition involves situations where the cursor indicating the individual's center of gravity on the device is either visible or hidden. The second condition examines whether the eyes-closed state during the test is achieved through voluntary eye closure or by external equipment (e.g., goggles or eye patches). The values obtained will allow comparisons of the effects of different sensory conditions on the sway index. The study will be conducted between January 2025 and March 2025 at the Bezmialem Vakıf University Cardiac Physiotherapy and Rehabilitation Education and Research Laboratory with healthy young adults. Participants will be selected voluntarily, and the assessments will be conducted in compliance with the guidelines of the Declaration of Helsinki.

Enrollment: 31 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Being between the ages of 18 and 45.
• Providing informed consent to participate in the study after receiving detailed information about the research.

Exclusion criteria

• Having visual or hearing impairments.
• Presence of musculoskeletal, neurological, or orthopaedic conditions (e.g., lower extremity alignment disorders, excessive anteversion, severe pes planus) that could affect the study results.
• Having mental or physical problems severe enough to impair communication.
• Participation in any rehabilitation program within the past six months.

Trial design

31 participants in 1 patient group

Study Group

Description:

Healthy Young Adults