Cardiovascular DiseasesNCT00005311
Hypertension in Minorities Database-Workshop and Publication
An observational study of Cardiovascular Diseases and Heart Diseases, run by National Heart, Lung, and Blood Institute (NHLBI).
Trial summary
To develop a comprehensive database publication (databook) utilizing available published and unpublished data on the prevalence of hypertension and its treatment and control in selected minority populations in the United States -- Hispanic, Asian and American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. Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Cardiovascular Diseases, Heart Diseases, Hypertension
- How many people
- Not given
- Where
- No sites listed yet
- Study dates
- Sep 1993to Mar 1996
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Men only
- No healthy volunteers
- Child, Adult, Older adult
No eligibility criteria
About this study
To develop a comprehensive database publication (databook) utilizing available published and unpublished data on the prevalence of hypertension and its treatment and control in selected minority populations in the United States -- Hispanic, Asian and American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.
Read the 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.
- Conditions
- Cardiovascular Diseases, Heart Diseases, Hypertension
- Medical subject headings
- Cardiovascular Diseases, Heart Diseases, Hypertension
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2000 (estimated)
- Study startSep 1993
- Study completionMar 1996
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Cardiovascular DiseasesStudies of the same condition, open and under way.
- More trials run by National Heart, Lung, and Blood Institute (NHLBI)The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
Sponsor and investigators
- Sponsor type
- US National Institutes of Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00005311
- Sponsor's protocol ID
- 4047
- Status last verified
- Jun 2000
- First submitted
- 25 May 2000
- Last updated
- 24 Jun 2005
- Results posted
- No
Publications
Keller JB. NHLBI workshop panel discussion: a scientific perspective. Public Health Rep. 1996;111 Suppl 2(Suppl 2):71-3.
PubMed 8898782US Dept of Health and Human Services, PHS, NIH: Hypertension in Hispanic Americans, American Indians and Alaska Natives, and Asian and Pacific Islander Americans. February, 1996.
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2005. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hypertension in Minorities Database-Workshop and Publication
- ClinicalTrials.gov ID
- NCT00005311
- Acronym / sponsor ID
- 4047
- Conditions
- Cardiovascular Diseases, Heart Diseases, Hypertension
- Study type
- Observational
- Recruitment status
- Completed
- Lead sponsor
- National Heart, Lung, and Blood Institute (NHLBI)US National Institutes of Health
- Study start
- Sep 1993
- Study completion
- Mar 1996
- First posted
- 26 May 2000 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
Who may qualify
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2005.
- Background: PubMed 8898782Keller JB. NHLBI workshop panel discussion: a scientific perspective. Public Health Rep. 1996;111 Suppl 2(Suppl 2):71-3.
- BackgroundUS Dept of Health and Human Services, PHS, NIH: Hypertension in Hispanic Americans, American Indians and Alaska Natives, and Asian and Pacific Islander Americans. February, 1996.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Cardiovascular Diseases and Heart Diseases, run by National Heart, Lung, and Blood Institute (NHLBI).
The full registered description is in the About this study section and the official record.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jun 2005. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00005311, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2005.