Usability of Virtual Reality in Subjects With Mild Cognitive Impairment or Alzheimer's Disease (MeMO-RV2)
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|ClinicalTrials.gov Identifier: NCT02176629|
Recruitment Status : Completed
First Posted : June 27, 2014
Last Update Posted : September 1, 2015
Cognitive and memory problems characterize Alzheimer's disease (AD). Along with these disorders, psychological and behavioral symptoms (also known as neuropsychiatric symptoms) , as well as pathophysiological processes are frequently found and involved significantly in maintaining autonomy, prognosis and treatment of the disease. Apathy or disorder motivation is the most common disorder behavior and early stages of cognitive impairment. Apathy is particularly associated with cognitive difficulties such as attention deficit disorder - concentration.
In terms of prevention as term care , there is now a broad consensus that interventions on cognition and behavior must not be limited to pharmacological treatment but should also promote non-drug approaches.
Interest in video games (serious games and serious games) as intervention support rehabilitation is growing. Similarly, the virtual reality (VR) and the new information technologies and communications offer significant opportunities in terms of rehabilitation and therapeutic assistance.
This protocol is part of a European project to propose techniques for improving the treatment of people at risk of social exclusion ( VERVE project ) aims .
A first experiment conducted in 2013 showed the acceptability of Virtual Reality (VR) in healthy elderly subjects. In a second step , it is important to validate the feasibility of using the RV or in frail subjects with mild cognitive impairment or Alzheimer's disease in mild to moderate in a clinical environment.
This is a biomedical , randomized given to a group of patients with mild cognitive impairment or Alzheimer's disease & diseases associated with mild to moderate.
|Condition or disease||Intervention/treatment||Phase|
|MCI Alzheimer's Disease||Other: Condition virtual reality (VR) then Condition classic cognitive stimulation (CCS) Other: Condition classic cognitive stimulation (CCS) then Condition virtual reality (VR)||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Official Title:||Usability of Virtual Reality in Subjects With Mild Cognitive Impairment or Alzheimer's Disease. MeMO-RV2|
|Study Start Date :||August 2014|
|Actual Primary Completion Date :||February 2015|
|Actual Study Completion Date :||February 2015|
Experimental: Condition virtual reality (VR)
The subject is placed in front of a Barcotm screen capable of displaying high quality images.
Other: Condition virtual reality (VR) then Condition classic cognitive stimulation (CCS)
Active Comparator: Condition classic cognitive stimulation (CSC)
It is proposed about using the test dam Zazzo suitable for elderly. This classic test measures sustained attention.
Other: Condition classic cognitive stimulation (CCS) then Condition virtual reality (VR)
- Evaluate the acceptability of the RV [ Time Frame: At the end of experience (45 min) ]
Analog scale assessment of satisfaction from 0 to 100% is given at the end of experience about that evaluates:
- The general acceptability of the RV
- His sense of security
- The environment of RV
- The degree of motivation
- Evaluate the motivation of subjects (interest, cognition) is greater in the virtual environment during the VR experience compared to a conventional cognitive stimulation activity (CSC). [ Time Frame: At the end of experience (45 min) ]
- Percentage of membership: relationship between time spent playing in the subject and the total time required by the experiment (Comparison of the two conditions (RV vs SCC));
- Degree of performance: number of "cognitive targets" found by the subject during the experiment. (Comparison of the two conditions (RV vs SCC));
- Degree of attention: the number of errors in target detection;
- Evaluation of the degree of presence of participants (condition RV) using the ITC-SOPI.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02176629
|Institut Claude Pompidou|
|Nice, France, 06000|
|Study Director:||Philippe ROBERT, PUPH||Centre Hospitalier Universitaire de Nice|