- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02884739
Mental Healthcare in Older Adults With Schizophrenia (CSA)
September 1, 2016 updated by: CHU de Reims
The Mortality and Its Associated Factors in Schizophrenia Patients Older Than 60 Years
As in the general population, there is a gradual and steady increase in life expectancy of patients with schizophrenia.
But this increase is at a smaller scale, with a rate of premature death that is still 2 to 3 times higher than that found in the general population.
This excessive early mortality is explained by an overrepresentation of suicide deaths, but also a higher prevalence of somatic diseases, mainly cardiovascular.
But today there are only very few epidemiological data on the mortality of patients with schizophrenia, including those aged over 60 years.
What are the sociodemographic and clinical characteristics (psychiatric and somatic) of these schizophrenic elderly patients?
Do they benefit from a somatic follow-up adequate and systematic?
What are their levels of social independence and of quality of life? the answers these questions and the description of the offer of geriatric care and of psychiatric care currently provided by different sectors of psychiatry in France is an indispensable prerequisite for any project to improve the quality of life, state of health and mortality of older patients with schizophrenia.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Evaluate prospectively over 5 years, the rates and causes of mortality in a cohort of schizophrenic patients older than 60 years, followed by adult psychiatry sectors, compared to those patients matched for sex and age and monitored by the same sectors for a chronic psychiatric disorder other than schizophrenia
Study Type
Observational
Enrollment (Actual)
685
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Reims, France, 51092
- CHU de Reims
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with schizophrenia and patients with chronic psychiatric disorder other than schizophrenia were included
Description
Inclusion Criteria:
- Men or women aged than 60 years with a diagnosis of schizophrenia, according to the DSM-IV criteria
- Men or women aged than 60 years with chronic psychiatric disorder other than schizophrenia
- Patients consenting to participate to the study
- Patients enrolled in the national healthcare insurance program
Exclusion Criteria:
-Disease affecting the central nervous system
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
schizophrenia
|
|
chronic psychiatric disorder other than schizophrenia
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Death
Time Frame: 5 years
|
Death of any causes
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Anticipated)
July 1, 2018
Study Completion (Anticipated)
July 1, 2018
Study Registration Dates
First Submitted
August 26, 2016
First Submitted That Met QC Criteria
August 26, 2016
First Posted (Estimate)
August 31, 2016
Study Record Updates
Last Update Posted (Estimate)
September 2, 2016
Last Update Submitted That Met QC Criteria
September 1, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PN08001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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