- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03120741
Dementia Patient's Behavior Evaluation Using Noninvasive Ambient Sensor
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Taipei, Taiwan, 10617
- National Taiwan University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
The age of the subject is over 65. The education level is junior high school degree or above. The healthy elders will be selected by the MMSE score (over 24), AD-8 score (under 2) and the Mini-Cog (over 4).
The MMSE score of the subjects with cognitive impairment or dementia is 10 to 23.
Description
Inclusion criteria:
- Can communicate in Mandarin or Taiwanese.
- Consciousness is clear.
- Can do the daily activity by their own.
Exclusion criteria:
- Have a serious cardiopulmonary disease or physical activity is limited to those unable to carry out daily activities.
- Consciousness is not clear.
- Difficult communication, such as: aphasia patients, the use of respirator patients.
- Suffering from serious mental illness that can not match.
- Adopt absolute isolation, such as: open tuberculosis patients.
- Hearing or severe visual impairment that can not match.
- Can not exercise their consent.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The relationship between moving pattern change and dementia.
Time Frame: 6 months
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Motion sensors will be installed on the ceiling.
We will analyze multiple sensors to see how the participant move from one location to another.
The data whether the participant is wandering or not and times of wandering will be measured.
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6 months
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The relationship between daily routine change and dementia.
Time Frame: 6 months
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Motion sensors, switch sensors, and current sensors will be installed in the home of the participant. The room which the participant is in, the appliance which the participant is using will be measured. |
6 months
|
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The relationship between sleeping time change and dementia.
Time Frame: 6 months
|
Motion sensors will be installed in the bed or on the ceiling.
The time when the participant goes to sleep, and the times the participant turns over during sleep will be measured.
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6 months
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Collaborators and Investigators
Investigators
- Principal Investigator: Li-Chen Fu, Doctor, National Taiwan University, Department of Computer Science & Information Engineering
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201608004RINB
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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