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Clinical Trials/NCT00743418
NCT00743418UnknownPhase 1

The Use of Advanced Tracking Technologies for the Analysis of Mobility in Alzheimer's Disease and Related Cognitive Disorders

Tel-Aviv Sourasky Medical Center1 site in 1 country300 target enrollmentStarted: June 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Enrollment
300
Locations
1
Primary Endpoint
Evaluation tools include: Geriatric Depression Scale, functional health questionnaire (SF-36), Emotional well-being questionnaire (Positive and Negative Affect Schedule; PANAS), single Life Satisfaction question and the Zarit Burden Interview

Study Overview

Brief Summary

The research is aimed at exploring the application of novel tracking technique for the study of spatial activity among dementia patients and its implication on their families. The study sample will be composed of three groups of volunteers, each including100 participants aged over 60 years. The first group will include MCI (Mild Cognitive Impairment) patients. The second group will include patients that suffer from mild dementia. The third group will include age matched healthy participants. The tracking equipment will be a GPS apparatus of 450 gms that will be carried by the participants for 24 hours along 2-4 weeks. The GPS data will be transferred via the cellular network to operator center at the Hebrew university at Jerusalem, and will be documented in assigned data files. This monitoring procedure will be held every year and along a period of five years. The impact of the patient behavior on the care giver will be studied by means of five interviews along the tracking period.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patients with MCI, Alzheimer's disease, or mixed type dementia; OR
  • •Healthy control subjects who meet the following criteria:
  • •Mini Mental State (MMSE) of at least 21
  • •Age 60 years or older
  • •Patients with history of stroke which is not followed by cognitive decline may be included
  • •Fluent language skills

Exclusion Criteria

  • •Other dementias (e.g. vascular, frontotemporal, metabolic etc);
  • •Other major psychiatric disorders (e.g. major depression, schizophrenia);
  • •Substance abuse;
  • •MMSE 20 or less;
  • •Severe motor disturbances;
  • •Sensory deficits potentially affecting mobility; OR
  • •Severe physical disorders (e.g. cancer, major operation)

Arms & Interventions

1

Other

Healthy controls Mini Mental State evaluation score >28/30

Intervention: GPS modem and RFID (Device)

2

Other

Mild Cognitive Impairment: Mini Mental State Evaluation Score (MMSE)=26-28/30

Intervention: GPS modem and RFID (Device)

3

Other

Mild Dementia: Mini Mental State Evaluation Score (MMSE)=21-25/30

Intervention: GPS modem and RFID (Device)

Outcomes

Primary Outcomes

Evaluation tools include: Geriatric Depression Scale, functional health questionnaire (SF-36), Emotional well-being questionnaire (Positive and Negative Affect Schedule; PANAS), single Life Satisfaction question and the Zarit Burden Interview

Time Frame: Before and after interventions

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov

Study Sites (1)

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