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Clinical Trials/NCT04819126
NCT04819126
Completed
Not Applicable

Nintendo Wii Virtual Reality Application In Older People With Alzheimer's Dementia

Kırıkkale University1 site in 1 country32 target enrollmentJanuary 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Age-Related Memory Disorders
Sponsor
Kırıkkale University
Enrollment
32
Locations
1
Primary Endpoint
Sex/Gender
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

•This study was planned to investigate the effects of the Nintendo Wii virtual reality application on muscle strength and fall risk in individuals with AD.

The aim of the present study is to investigate the effect of the virtual reality application on muscle strength and fall in individuals with Alzheimer' Dementia (AD).

Detailed Description

Purpose: This study was planned to investigate the effects of the Nintendo Wii virtual reality application on muscle strength and fall risk in individuals with AD. Method: The study included a total of 32 volunteers between the ages of 65-80, with mild or moderate AD diagnosed. These individuals were divided into 2 groups as a training group and control group. The training group was trained with games from different categories such as balance and aerobic exercises with a Nintendo Wii virtual reality device 2 times a week for a period of 6 weeks, with 1 session lasting for 30 minutes. Mini-Mental State Test, Knee Extension Muscle Strength, Timed Up and Go Test, Tinetti Falls Efficacy Scale results of individuals were recorded in the evaluation.

Registry
clinicaltrials.gov
Start Date
January 15, 2018
End Date
January 15, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kırıkkale University
Responsible Party
Principal Investigator
Principal Investigator

Meral SERTEL

Kırıkkale University

Kırıkkale University

Eligibility Criteria

Inclusion Criteria

  • included volunteers between the ages of 65-80 with mild or moderate AD diagnosis,
  • who did not have any difficulty or problems in communicating,
  • who did not have any neurological diseases that disrupt balance and coordination such as a cerebrovascular event, Parkinson's disease, Multiple Sclerosis, and neurological disorder,
  • who obtained a score of 18 - 24 points in the Mini-Mental State Test (MMST)

Exclusion Criteria

  • Patients diagnosed with rapidly progressing dementia (infection, vascular, hematologic diseases),
  • Those who could not be contacted during the follow-up period or who did not participate in the training session, those who experienced cardiac and cerebrovascular events, endocrine disorders, fluid-electrolyte imbalance and infection,
  • Those with malignancy and those who received chemotherapy and radiotherapy that causes malignancy, delirium or depression and malignant sensory loss (those with the Semmes-Weinstein monofilament thickness of 4.56 and above),
  • Those with a lower or upper extremity amputation at any level

Outcomes

Primary Outcomes

Sex/Gender

Time Frame: period of 6 weeks

Sex: Female, Male

Age :mean or median age

Time Frame: period of 6 weeks

Age, Categorical: \>=65 years

Body Mass Index

Time Frame: period of 6 weeks

BMI was recorded in kg/m\^2.

Secondary Outcomes

  • The Mini-Mental State Test for Cognitive status(period of 6 weeks)

Study Sites (1)

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