Viewing Study NCT00005685



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Study NCT ID: NCT00005685
Status: COMPLETED
Last Update Posted: 2016-05-13
First Post: 2000-05-25

Brief Title: Blood Pressure Control--Racial and Psychosocial Influences
Sponsor: National Heart Lung and Blood Institute NHLBI
Organization: National Heart Lung and Blood Institute NHLBI

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2006-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To examine racial and psychosocial influences on blood pressure control
Detailed Description: BACKGROUND

Environmental and psychosocial factors relating to hypertension and cardiovascular disease are incompletely understood particularly for women and African Americans Recent research has suggested that job strain is more strongly linked to elevated work blood pressure in men than women In contrast the combination of having a high status job plus the trait of high effort coping style John Henryism was related to higher work blood pressure in women and African American men but not Caucasian men

The grant has been ongoing since September 1983 The original study had as its purpose to ascertain similarities and differences in the etiology of hypertension for Blacks and whites and to identify those biobehavioral factors contributing to the excess risk for hypertension among Blacks Myocardial blood pressure and renal responses sodium and potassium handling to laboratory and naturalistic stressors were evaluated in young adult normotensive or marginally hypertensive Black and white men Behavioral stressors included competitive reaction time tasks active coping as well as more passive coping conditions Data were collected on family history of hypertension family social class background Type A behavior propensity for anger and hostility and coping style The role of the sympathetic nervous system in mediating these effects was assessed by the use of beta-adrenergic antagonists

When the grant was renewed in 1991 the goal of the research was to evaluate the interactive effects of environmental stressors and sodium chloride NACl and potassium K intake as they related to hypertension development in a biracial population

DESIGN NARRATIVE

There were two studies in the current grant Study 1 reexamined hypothesized relationships of high effort coping and job strain to elevated ambulatory blood pressure BP at work and at home in a sample of 288 Black and white men and women stratified by job status Also assessments were made of the relationships of these traits to increased epinephrine and norepinephrine responses other measures of sympathetic activation adverse lipid profiles and cardiac and vascular structural changes Job strain and high effort coping were also related to hypertension prevalence in 576 black and white men and women stratified by job status The influence of additional psychosocial variables social support hostility anger-in depressed mood anxiety was also examined

Study 2 built on prior research on gender differences in total peripheral resistance during stressors which enhance alpha-adrenergic activity and on a recent observation that among young adults slow sodium excretion during stress is seen in five times as many men as women It also built on recent work suggesting that estrogen may attenuate total peripheral resistance responses to stress by reducing vasoconstrictive effects of alpha-adrenergic activity The study was designed to examine cardiovascular lipid epinephrine norepinephrine and sodium excretion responses to stressors in 120 subjects maintained for a week on a controlled high salt diet Thirty subjects were tested in each of these groups 1 premenopausal women 2 postmenopausal women not using hormone replacement therapy 3 postmenopausal women using hormone replacement 4 men Each group included 15 Black and 15 white subjects and each subject was tested twice once after receiving placebo and once after receiving either an alpha- or a beta-receptor antagonist

The study completion date listed in this record was obtained from the End Date entered in the Protocol Registration and Results System PRS record

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
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Secondary IDs
Secondary ID Type Domain Link
R01HL031533 NIH None httpsreporternihgovquickSearchR01HL031533