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Prognostic Measures in Ambulatory Care Settings

Prognostic Measures in Ambulatory Care Settings

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00195130
Enrollment
2000
Registered
2005-09-19
Start date
1998-01-31
Completion date
1999-01-31
Last updated
2008-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

General Internal Medicine Patients

Keywords

prognosis, risk of death, morbidity, mortality, quality of life

Brief summary

The primary objective of this prospective study is to develop a new method of classifying the prognosis of ambulatory patients according to their risk of long term mortality, institutionalization, morbidity (including the deterioration of pre-existing conditions or development of new problems) and functional deterioration.

Detailed description

Specifically, from a random sample of 2000 patients taken from a cohort of established patients followed for at least three years in a general medicine practice, the objectives are: 1. to identify the demographic, clinical, and functional status variable that predict the risk of death, morbid events (e.g., the development of new complications or deterioration of existing conditions), or the deterioration in functional status using a half of the cohort chosen at random; 2. to combine these findings into a prognostic scale that can be employed in routine clinical practice; and 3. to validate the performance of this scale in the second half of the cohort. There are no interventions in this study. Patients already under medical care by Cornell physicians will be enrolled. The only requirements for patients are to complete the questionnaires on an annual basis.

Interventions

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1\. Patients who are currently under the care of Physicians at Cornell Internal Medicine Associates.

Exclusion criteria

1. Patients who do not wish to participate in the study. 2. Patients who are not able to provide informed written consent.

Design outcomes

Primary

MeasureTime frame
To develop a new method of classifying the prognosis of ambulatory patients according to their risk of long term mortality, institutionalization, morbidity and functional deterioration.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026