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Clinical Trials in Turkey / NCT07466615
Starting soon Not applicable

Sensory Integration Training for Older Adults With Mild Cognitive Impairment

NCT07466615 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-03-12

Condition(s) studied

Mild Cognitive Impairment (MCI)

Investigational drug(s) / intervention(s)

Aerobic ExerciseSensory Integration Training

Aerobic Exercise: The aerobic exercise intervention consists of a 12-week outdoor walking program, performed twice weekly for 45 minutes per session at a moderate intensity, targeting a score of 12-14 on the Borg Rating of Perceived Exertion (RPE) scale

Sensory Integration Training: The program includes activities that stimulate three main senses: vestibular (balance and movement), proprioceptive (body awareness), and tactile (touch). These exercises are designed to help the brain organize sensory signals more effectively to improve daily functions and cognitive performance.

Study summary

This study aims to investigate the effects of sensory integration training on cognitive functions, quality of life, and social participation in older adults with Mild Cognitive Impairment (MCI)

Eligibility

Sex
ALL
Min age
65 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * Being between 65 and 85 years of age * Having a Montreal Cognitive Assessment (MoCA) score between 18 and 25, indicating mild cognitive impairment * Being in stable medical health, with no history of severe neurological or psychiatric disorders * Voluntary participation Exclusion Criteria: * Clinical diagnosis of dementia or having moderate-to-severe cognitive impairment * Severe visual or hearing loss to a degree that prevents effective communication or participation in assessments * Presence of severe sensory, motor, or physical disabilities that render the intervention (e.g., walking or sensory training) impossible to perform * Acute medical conditions or having unstable chronic diseases that may pose a risk during physical activity.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Isparta Şehir Hastanesi Isparta Merkez

More Akdeniz University trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07466615 on ClinicalTrials.gov ↗ ← All trials in Turkey