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Recruiting NCT07045259

NCT07045259 Effect of Exergaming Program Versus Neuromuscular Exercise in Elderly People With Motor Cognitive Risk Syndrome

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Clinical Trial Summary
NCT ID NCT07045259
Status Recruiting
Phase
Sponsor Istanbul University - Cerrahpasa
Condition Motoric Cognitive Risk Syndrome
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-12-25
Primary Completion 2026-03-25

Eligibility & Interventions

Sex All sexes
Min Age 65 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
The Neuromuscular Exercise Training programExergaming Exercise Training

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2025-12-25 with a primary completion date of 2026-03-25.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary aim of our study is to compare the effects of neuromuscular exercise training versus structured exergaming program on locomotor and cognitive functions in elderly individuals with Motor Cognitive Risk (MCR), which defines the transition state between typical aging and dementia and mild cognitive impairment. This study aims to present for the first time the effects of neuromuscular exercise training and exergaming program on locomotor and cognitive functions in elderly individuals with MCR with comparative results.

Eligibility Criteria

Inclusion Criteria: * Being over 65 years of age * Having a Barthel Daily Living Activities Index score of ≥ 90 * Having a Mini Mental Status Score (MMSE) of ≥24 * Having the ability to walk with or without a walking aid * Having a slow walking speed * Having subjective memory complaints Exclusion Criteria: * Presence of Dementia * Major Depression * Generalized Anxiety Disorder and Delirium * Parkinson's Disease * Anemia * Thyroid Disease * Vitamin B12 Deficiency * Malnutrition * Terminal Illness * Hearing or Visual Impairment

Contact & Investigator

Central Contact

GULFİDAN TOKGÖZ, Lecturer, PhD (c)

✉ gulfidan.tokgoz@gmail.com

📞 +90552 022 76 32

Principal Investigator

Gulfidan TOKGÖZ, Lecturer, PhD (c)

PRINCIPAL INVESTIGATOR

İstanbul University-Cerrahpasa

Frequently Asked Questions

Who can join the NCT07045259 clinical trial?

This trial is open to participants of all sexes, aged 65 Years or older, studying Motoric Cognitive Risk Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07045259 currently recruiting?

Yes, NCT07045259 is actively recruiting participants. Contact the research team at gulfidan.tokgoz@gmail.com for enrollment information.

Where is the NCT07045259 trial being conducted?

This trial is being conducted at Balıkesir, Turkey (Türkiye).

Who is sponsoring the NCT07045259 clinical trial?

NCT07045259 is sponsored by Istanbul University - Cerrahpasa. The principal investigator is Gulfidan TOKGÖZ, Lecturer, PhD (c) at İstanbul University-Cerrahpasa. The trial plans to enroll 60 participants.

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