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| Sponsor: | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00006498 |
Purpose
To prospectively examine the association between a specific chronic life stressor (i.e., intimate violence exposure) and adult asthma in women.
| Condition |
|---|
|
Asthma Lung Diseases |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Observational Model: Natural History Time Perspective: Longitudinal |
| Study Start Date: | September 2000 |
| Estimated Study Completion Date: | August 2005 |
BACKGROUND:
Etiologies of the rising prevalence and morbidity of asthma are not well understood. Knowledge gaps are particularly significant with respect to adult-onset asthma. The role of stress in the expression of asthma is largely unexplored in large-scale, prospective, epidemiologic studies and such investigation has been identified as a priority by a recent NHLBI expert panel.
DESIGN NARRATIVE:
The study prospectively examines the association between a specific chronic life stressor (i.e., intimate violence exposure) and adult asthma in women participating in the Nurses' Health Study II cohort. Emerging epidemiologic data suggest that exposure to intimate violence is a pervasive chronic life stressor associated with adverse impact on womens' psychological and physical health. Traumatic stress such as that related to intimate violence exposure has been associated with neuroendocrine changes known to cause alterations in neuroendocrine and immune functions important to the pathophysiology of inflammatory diseases including asthma. The investigators are testing the hypothesis that women exposed to high-level chronic stress (violence) will be at greater risk for asthma development than women with low-level stress (violence) exposure. The influence of chronic stress on neuroendocrine and immune function as reflected in morning cortisol expression, for the former, and cytokine profiles and IgE production (T-helper cell polarization), for the latter, will also be examined in a nested case control fashion among these women.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
No eligibility criteria
Contacts and Locations
More Information
| ClinicalTrials.gov Identifier: | NCT00006498 History of Changes |
| Other Study ID Numbers: | 939 |
| Study First Received: | November 16, 2000 |
| Last Updated: | January 27, 2006 |
| Health Authority: | United States: Federal Government |
|
Asthma Lung Diseases Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |