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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01076855
Other study ID # 2010/008
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2010
Est. completion date December 2015

Study information

Verified date December 2022
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the programme is to facilitate the anticipation of dementia both in elderly patients suffering from this disease and in their carers and to diminish care burden in order to improve quality of life and daily functioning.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria: - elderly (> 70 years) with mild dementia in presence of a carer.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life and care burden at 0, 3 and 6 months. 0, 3 and 6 months
Secondary Cognitive, behavioural and affective status 0, 3 and 6 months
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