Alzheimer's Disease (AD) Clinical Trial
Official title:
Cognitive-motor Intervention Using Virtual Reality for Middle-aged Individuals at High Dementia Risk
The primary objective of this program is to apply a virtual reality (VR) cognitive-motor intervention (compared to active and passive control groups) to delay or slow cognitive decline of middle-aged adults who have a family history of Alzheimer's disease (AD) and thus are at particularly high risk of developing the disease.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | August 2019 |
Est. primary completion date | July 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 40 Years to 65 Years |
Eligibility |
Inclusion Criteria: - The participants of the study must have at least one parent with Alzheimer's disease. - Fluency in Hebrew, in order to understand the instructions of the cognitive tests. - Availability of an informant for the participant. Exclusion Criteria: - Severe neurological or psychological conditions that may affect cognitive performance. - Substantial orthopedic limitations which prevent the use of treadmill. - Unstable medical condition such as an active cancer. - Incapability of adherence to the training program. - The participant is undergoing a treatment that may interfere with the study program. |
Country | Name | City | State |
---|---|---|---|
Israel | Sheba Medical Center | Ramat Gan |
Lead Sponsor | Collaborator |
---|---|
Sheba Medical Center |
Israel,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in overall cognition- measured by averaging z-scores from 14 paper and pencil neuropsychological tests covering episodic memory and executive functions cognitive domains. | summary of the z-scores of all 14 paper and pencil cognitive tests | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Primary | change in cerebral blood flow from arterial spin labeling (ASL) | acquired by structural MRI using background-suppressed pseudo-continuous ASL (pcASL) featuring a 3D fast spin echo spiral sequence | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | specific cognitive domains- average of z-scores of paper and pencil memory tests and of executive functions tests | summary of z-scores of executive functions tests and of episodic memory tests | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | blood oxygenation level dependent (BOLD) functional MRI (fMRI) signal in the fronto-parietal network associated with working memory | T2*-weighted fMRI during an n-back working memory task; contrasts: 1-back minus 0-back; 2-back minus 0-back; 2-back minus 1-back | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | brain resting state functional connectivity by resting state network fMRI BOLD signal correlations | T2*-weighted fMRI while relaxing with eyes closed; functional connectivity between seed regions of resting state networks (e.g., default mode, attentional, salience) and other regions by correlation of BOLD signal in seed regions with that in other regions | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | hippocampal volume | 3D T1-weighted MRI imaging | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | frontal inferior cortex volume | 3D T1-weighted MRI imaging | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | white matter hyperintensity (WMH) burden | 3D T2-FLAIR MRI imaging | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) | |
Secondary | diffusion-tensor imaging (DTI) measures | diffusion-weighted MRI imaging (DWI) to map white matter tractography | baseline, immediately after 12-week training, and 3 months post-training (or corresponding time points in passive control group) |
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