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Clinical Trials/NCT02893800
NCT02893800
Completed
Not Applicable

Assistive Technology for Dementia: Validation and Optimization of the Individual Benefits of Locating Systems in Dementia Care (VODINO)

Charite University, Berlin, Germany1 site in 1 country40 target enrollmentJune 2016
ConditionsDementia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dementia
Sponsor
Charite University, Berlin, Germany
Enrollment
40
Locations
1
Primary Endpoint
Usability
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The project aims to make new technologies for locating people with dementia easier to use for the patients and those caring for them.

Objective: To systematically understand what improves the user experience of persons with dementia (PwD) and their primary caregivers (CG) with locating system watches to ultimately allow users to obtain more benefits from using these watches.

Aim: Improving the user experience of PwD and CG with locating system watches using a cross-over design and a theory-based educational session approach.

Detailed Description

This entire research field (assistive technology in dementia care) is based on the need to address care solutions for a growing number of PwD and CG in the absence of a cure for (Alzheimer's) dementia. Methods: A user study with two free available locating watches. In educational sessions PwD obtain a locating watch and their CG a smartphone with the application of the locating watch installed on it. By using a cross-over design each dyad (PwD and CG) obtaining both locating systems. The designed educational session hopefully ease subsequent use and make it more enjoyable. The dyads will use each system over four weeks in their real environment.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
November 2016
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Oliver Peters, MD

MD

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • diagnosis of all kinds of dementia or mild cognitive impairment

Exclusion Criteria

  • not able to move outside alone

Outcomes

Primary Outcomes

Usability

Time Frame: 8 weeks

ISONORM 9241/10 questionnaire (Prümper, 1997)

Secondary Outcomes

  • Acceptance and Practicability(8 weeks)
  • Activities of Daily Living(8 weeks)
  • Caregiver burden(8 weeks)
  • Subjective quality of life(8 weeks)

Study Sites (1)

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