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Prevalence, Awareness and Management of Hypertension in Acute Care Personnel

Prevalence, Awareness and Management of Hypertension in Acute Care Personnel

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01655654
Enrollment
160
Registered
2012-08-02
Start date
2012-08-31
Completion date
2013-07-31
Last updated
2020-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Hypertension, Acute hospital staff, Exercise, Diet

Brief summary

The primary purpose of this study is to identify the percentage of health care workers working in an acute care hospital who have high blood pressure, to determine the awareness of their blood pressure status, and to see how well it is managed. Study participants will come from the following three distinctly different types of departments: telemetry (clinical), non-telemetry (clinical), and non-direct patient care staff. All study participants are offered educational information surrounding high blood pressure and review the recommendation for their primary care engagement. Study participants with high blood pressure will be asked to continue in the study for up to 6 months. It is intended that each study participant who continues will take their blood pressure three times a day and record the results in a study provided diary. Each study participant should also make some of the suggested changes that promote a healthier lifestyle including exercising, improving their diet, and seeing their primary care provider. It is the thought that these changes will reduce the study participant's blood pressure. The secondary purpose is to determine the effect shift work has on these hospital employees and the potential positive effects of the three interventions.

Detailed description

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.

Interventions

BEHAVIORALPhysical activity

This intervention includes cardiorespiratory exercise, resistance exercise, flexibility exercise and neuromotor exercise.

BEHAVIORALDietary

Make at least one positive dietary change including or similar to a DASH diet snack substitution.

OTHERPrimary 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.

Sponsors

Providence Health & Services
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Providence Health System's Southwest Washington Service Area (SWSA) employees * Subjects who will be included in the intervention part of the study will have two consecutive BP readings of \> 140/90 * Has or is willing to have collaborative PCP * Understand and sign the informed consent form

Exclusion criteria

* Under the age of 18 * Has a severe systemic illness with life expectancy judged less than three years * Has a severe vascular event such as Myocardial Infarction or Cerebral Vascular Event in the past 90 days * Is enrolled in another therapeutic program or similar study, and * Has a condition which, in the opinion of the investigators, may prevent the subject from participating in the study

Design outcomes

Primary

MeasureTime frameDescription
Reduction of blood pressure6 monthsThe 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026