Prevalence, Awareness and Management of Hypertension in Acute Care Personnel
|ClinicalTrials.gov Identifier: NCT01655654|
Recruitment Status : Unknown
Verified May 2013 by Providence Health & Services.
Recruitment status was: Active, not recruiting
First Posted : August 2, 2012
Last Update Posted : May 22, 2013
|Condition or disease||Intervention/treatment||Phase|
|Hypertension||Behavioral: Physical activity Behavioral: Dietary Other: Primary care provider visit||Not Applicable|
Research on hypertension (HTN) in hospital personnel during work hours is limited yet research has been published on the relationship of job strain and the risk of cardiovascular disease. HTN can be caused by sympathoadrenal activation brought on by long-term exposure to stressors and an inherent biomarker that is associated with an increased risk of cardiovascular disease.
The primary purpose of this study is to quantify differences in HTN prevalence, awareness and management in three distinctly different areas and shifts within an acute hospital. Blood pressure (BP) will be taken during working hours along with pre and post sleep hours. The secondary purpose is to identify the effect of shift work within an acute care hospital and effectiveness of: BP monitoring, increases in physical activity, positive nutritional changes, and the correlation between a primary care provider visits and lowering BP.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||160 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Prevalence, Awareness and Management of Hypertension in Acute Care Personnel|
|Study Start Date :||August 2012|
|Estimated Primary Completion Date :||July 2013|
|Estimated Study Completion Date :||July 2013|
No Intervention: Cohort 1
All employees within the acute care hospital that signed the informed consent form and provided their individual data.
Active Comparator: Cohort 2
All subjects of cohort 1 who also are considered hypertensive and participated in one or more study interventions, which include behavioral interventions (an increase in physical activity, or dietary changes) or who have a primary care provider visit to discuss hypertension.
Behavioral: Physical activity
This intervention includes cardiorespiratory exercise, resistance exercise, flexibility exercise and neuromotor exercise.Behavioral: Dietary
Make at least one positive dietary change including or similar to a DASH diet snack substitution.Other: Primary care provider visit
Subjects with hypertension will be asked to visit their primary care provider seeking treatment options. If a subject does not have a primary care provider then they will be encouraged to obtain one and seek medical treatment.
- Reduction of blood pressure [ Time Frame: 6 months ]The study will look for a reduction in blood pressure during a 6-month time frame among those identified at screening to have high blood pressure and who continue on in the study.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01655654
|United States, Washington|
|Providence St. Peter Hospital|
|Olympia, Washington, United States, 98506|
|Principal Investigator:||Dan Donahue, M.Ed.||Providence Health and Services|