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Sponsors and Collaborators: |
Martin-Luther-Universität Halle-Wittenberg German Federal Ministry of Education and Research |
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Information provided by: | Martin-Luther-Universität Halle-Wittenberg |
ClinicalTrials.gov Identifier: | NCT00644826 |
The purpose of this study is to determine whether preventive home visits for people aged 80 and over are effective in the prevention of nursing home admission in Germany.
Condition | Intervention |
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Aging |
Behavioral: preventive home visit |
Study Type: | Interventional |
Study Design: | Supportive Care, Randomized, Single Blind (Outcomes Assessor), Parallel Assignment |
Official Title: | Growing Old at Home - Effectiveness and Cost-Effectiveness of Preventive Home Visits to Reduce Nursing Home Admissions in the Elderly |
Estimated Enrollment: | 320 |
Study Start Date: | September 2007 |
Estimated Study Completion Date: | December 2009 |
Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Experimental |
Behavioral: preventive home visit
A multidimensional geriatric assessment within the dimensions: cognition, health related functioning, risk of falling, nutritional status, social situation, economic situation, mood. Two more home visits: (1) home counseling visit 2-3 weeks after assessment (2) booster session 1 month after home counseling visit
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2: No Intervention |
Regarding demographic changes in Germany it can be assumed that the number of elderly and the resulting need for long term care is increasing in the near future. It is not only an individual's interest but also of public concern to avoid a nursing home admission. Current evidence indicates that preventive home visits can be an effective way to reduce the admission rate in this way making it possible for elderly people to stay longer at home than without home visits. As the effectiveness and cost-effectiveness of preventive home visits strongly depends on existing services in the social and health system existing international results cannot be merely transferred to Germany. Therefore it is necessary to investigate the effectiveness and cost-effectiveness of such an intervention by a randomized controlled trial in Germany.
Ages Eligible for Study: | 80 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Germany, SA | |
Klinik und Poliklinik für Psychiatrie, Universitätsklinikum Leipzig AöR | |
Leipzig, SA, Germany, 04107 | |
Germany, SAN | |
Institut für Gesundheits- und Pflegewissenschaft, Medizinische Fakultät, Martin-Luther-Universität Halle-Wittenberg | |
Halle, SAN, Germany, 06197 |
Principal Investigator: | Johann Behrens, PhD | Martin-Luther-Universität Halle-Wittenberg |
Principal Investigator: | Steffi Riedel-Heller, MD | Universität Leipzig |
Responsible Party: | Martin-Luther-Universität Halle-Wittenberg ( Prof. Dr. phil habil Johann Behrens ) |
Study ID Numbers: | PfVMS-T5 |
Study First Received: | March 26, 2008 |
Last Updated: | October 2, 2008 |
ClinicalTrials.gov Identifier: | NCT00644826 History of Changes |
Health Authority: | Germany: Federal Ministry of Education and Research |
randomized controlled trial public health Preventive Health Services |