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UnknownNCT00693888

Lighthouse Project on Dementia, Ulm, Germany

Lighthouse Project on Dementia, Ulm, Germany - Improvement of Advice and Diagnostics for People Suffering From Dementia After the Classification of Their Level of Care (ULTDEM Study).

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
University of Ulm · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

The Geriatric Center Ulm scientifically supported a three-year pilot study (ProjektDEMENZ Ulm), in which numerous findings on the system of care regarding people suffering from dementia and their relatives were determined. One of the most important conclusions is the significant lack of information on the well-functioning network of the care system in Ulm. The full potential of the network is not being exploited. The situation in the Alb-Donau-Kreis - the area surrounding Ulm - is very similar. The investigators' aim is to improve the utilization of the system of care for those suffering from dementia in Ulm/Alb-Donau-Kreis by using a newly designed advisory approach (Lighthouse Project on Dementia, Ulm, ULTDEM study). The purpose of the study is to prove the effectiveness of this procedure by using a prospective, open, randomized, controlled, interventional study. After the randomization, the interventional group is given comprehensive, individual advice about available treatment possibilities for people suffering from dementia. In addition, they have the opportunity to re-evaluate their present diagnostic procedure. The participants of the control group receive the standard treatment. Inclusion criterion is the application of a care level ( level 0 or 1). Recruitment will take one year. A final assessment will be taken every six months.

Conditions

Interventions

TypeNameDescription
BEHAVIORALadvice (e.g. medical and social aspects, care, support at home, residential advice, legal aspects, demonstration of help and support for the relatives)initial comprehensive assessment, stratified (city, suburbs) randomization into two groups: interventional group: individual comprehensive primary advice (medical and social aspects, care, support at home, residential advice, legal aspects, demonstration of help and support for the relatives), control group: standard support, observation over a period of 6 months, possibility of completing the diagnostic after final assessment

Timeline

Start date
2008-06-01
Primary completion
2010-02-01
Completion
2010-09-01
First posted
2008-06-09
Last updated
2010-08-17

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00693888. Inclusion in this directory is not an endorsement.