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Clinical Trials in Turkey / NCT07433608
Recruiting Not applicable

Video Game Intervention In Older Adults

NCT07433608 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-17
Last updated
2026-03-06

Condition(s) studied

HealhtyAgingBalanceSelf EfficacyVisual Motor Integration

Investigational drug(s) / intervention(s)

Game-Based Virtual Reality Intervention

Game-Based Virtual Reality Intervention: The intervention consists of a structured rehabilitative game-based training program delivered using the BeCure system. The program includes interactive tasks that require active weight shifting, postural control, coordinated upper and lower extremity movements, and visually guided motor responses. The intervention will be implemented over a 6-week period, with sessions conducted twice per week. Each session will last approximately 30 minutes. Task difficulty will be progressively adjusted according to participant performance to maintain engagement and provide an appropriate level of challenge. The training sessions will be conducted individually under supervision. Real-time visual feedback provided by the system will enable participants to monitor their performance during task execution. No additional rehabilitation program will be provided concurrently within the scope of this study.

Study summary

The purpose of this clinical trial is to investigate the effects of a rehabilitative game-based intervention on self-efficacy, balance, and visual-motor integration in individuals aged 60 years and older.

The primary research questions are:

Does the rehabilitative game-based intervention improve balance and visual-motor integration? Does the rehabilitative game-based intervention improve self-efficacy levels?

Researchers will compare a rehabilitative game intervention group with a control group. Participants will complete baseline and post-intervention assessments. Individuals in the intervention group will participate in rehabilitative game sessions twice per week for 6 weeks, while the control group will not receive any intervention.

Eligibility

Sex
FEMALE
Min age
60 Years
Max age
69 Years
Healthy volunteers
Accepted
Inclusion Criteria: Age 60 years or older A score of 24 or higher on the Mini Mental State Examination (MMSE) Ability to understand and follow verbal instructions Willingness to participate voluntarily Exclusion Criteria: Presence of a neurological, orthopedic, or psychiatric diagnosis Medical contraindications to exercise Diagnosis of dementia Acute orthopedic injury Visual or hearing impairment that would interfere with participation Inability to attend sessions regularly

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Biruni University Istanbul Zeytinburnu Recruiting

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Other trials for the same condition

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 NCT07433608 on ClinicalTrials.gov ↗ ← All trials in Turkey