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Hypertension in Minorities Database-Workshop and Publication

This study has been completed.
Sponsor:
Information provided by:
National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier:
NCT00005311
First received: May 25, 2000
Last updated: June 23, 2005
Last verified: June 2000
  Purpose

To develop a comprehensive database publication (databook) utilizing available published and unpublished data on the prevalence of hypertension and its treatment and control in selected minority populations in the United States -- Hispanic, Asian and American Indian.


Condition
Cardiovascular Diseases
Heart Diseases
Hypertension

Study Type: Observational

Resource links provided by NLM:


Further study details as provided by National Heart, Lung, and Blood Institute (NHLBI):

Study Start Date: September 1993
Estimated Study Completion Date: March 1996
Detailed Description:

BACKGROUND:

Data on hypertension among minority populations were lacking prior to the workshop and databook publication. Several reasons why the data were lacking include the biological and cultural diversity of America's minorities, their wide dispersal across the country, and the fact that key data such as death certificate information have sometimes not been recorded.

DESIGN NARRATIVE:

The objective was accomplished in a two-phase approach as follows: Phase l. In June, 1994 a workshop was held in Washington, D.C. on the epidemiology of hypertension in minorities. The workshop, entitled "The Epidemiology of Hypertension in Hispanic Americans, Native Americans, and Asian/Pacific Islander Americans" included as participants the investigators who had relevant datasets and were willing to participate in the effort. The investigators were requested to use common definitions of hypertension in their workshop presentations when feasible. In addition, in preparation for a databook publication, each study was asked to provide summary data, using common definitions and a common format, on the prevalence of hypertension in the study population. Data presentations and interpretations at the workshop enabled the investigators and consultants to identify further research needs, further feasible data analyses utilizing available data, and special target groups for demonstration research efforts to enhance the potential success of intervention efforts.

Phase 2. A database publication (databook) was designed to include a summary of the workshop proceedings with the appropriate data and interpretations along with summary data from the studies presented in a standard, unified format. The databook, entitled "Hypertension in Hispanic Americans, American Indians and Alaska Natives, and Asian and Pacific Islander Americans" was published in 1996 and presented the prevalence of hypertension and its treatment and control by age, sex, and minority status, along with other information the planning committee considered relevant.

  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

No eligibility criteria

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

Publications:
ClinicalTrials.gov Identifier: NCT00005311     History of Changes
Other Study ID Numbers: 4047
Study First Received: May 25, 2000
Last Updated: June 23, 2005
Health Authority: United States: Federal Government

Additional relevant MeSH terms:
Cardiovascular Diseases
Heart Diseases
Hypertension
Vascular Diseases

ClinicalTrials.gov processed this record on November 25, 2014