A Web-Based Cardiovascular Intervention for the Workplace
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|ClinicalTrials.gov Identifier: NCT00763308|
Recruitment Status : Unknown
Verified September 2008 by National Heart, Lung, and Blood Institute (NHLBI).
Recruitment status was: Not yet recruiting
First Posted : September 30, 2008
Last Update Posted : September 30, 2008
|Condition or disease||Intervention/treatment||Phase|
|Cardiovascular Diseases||Behavioral: Web-based Heart Healthy Program||Phase 1|
Heart disease, or cardiovascular disease, refers to a range of diseases including coronary artery disease, heart attack, heart failure, high blood pressure, and stroke. These diseases are all related to problems with the heart and blood vessels, and collectively are the leading cause of death in the United States. Heart attacks or coronary artery disease sometimes have warning signs, but both can occur without warning. Approximately half of all heart attacks are fatal. Forty percent of all deaths in the United States are the result of heart disease.
Certain factors can predict whether people get heart disease. Some of these factors, like biological sex or genes inherited from a person's family, cannot be changed, but many others can. Not smoking, eating well, exercising regularly, and maintaining a healthy weight are some of the things people can do to lower their risk of heart disease. This study will develop and then test an Internet-based program that teaches people about heart health and supports them in changing behaviors that put them at risk for heart disease.
This study will be divided into two phases. In the first phase, researchers will create the Heart Healthy program, show it to focus groups, and try to improve it based on their comments. The goals of the program are to educate users in the fundamentals of heart health and risk factors for heart disease and to provide a system for starting and sustaining lifestyle changes that reduce risk of heart disease. The program will be designed for employee use in a workplace, and a tool kit will be developed for managers to supplement the employee program. The prototype will include modified segments from existing Web-based programs created by a non-profit organization, the ISA Group. The design of the program will be guided by feedback from employees and managers who use it and from experts in cardiology and epidemiology.
In the second phase, the program will be tested in a work site. Employees at risk for heart disease will be recruited and randomly assigned to receive either the Healthy Heart program or treatment as usual. Before and after the intervention, participants will be assessed on knowledge gained, attitudes changed, alterations in health behavior, and reductions in cardiovascular risk. Managers who receive the supplementary program will be tested in knowledge gained and plans for policy or procedural changes. The ultimate goal of this phase is to fully develop the Healthy Heart program for use in industry and health care settings.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||300 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Fast Track Program to Create a Web-Based Cardiovascular Intervention for the Workplace|
|Study Start Date :||April 2009|
|Estimated Primary Completion Date :||February 2010|
|Estimated Study Completion Date :||February 2010|
Participants will use the Web-based Heart Healthy program.
Behavioral: Web-based Heart Healthy Program
The Heart Healthy program will be developed during the course of the study based on goals set by researchers and based on feedback from focus groups. The goals of the program are to educate users in the fundamentals of heart health and risk factors for heart disease and to provide a system for starting and sustaining lifestyle changes that reduce risk of heart disease.
No Intervention: 2
Participants will receive treatment as usual.
- Change in health attitudes and behaviors [ Time Frame: Measured pre- and post-intervention ]
- Change in cardiovascular risk status [ Time Frame: Measured pre- and post-intervention ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00763308
|Contact: Diane K. Deitz, PhDemail@example.com|
|United States, Virginia|
|ISA Associates, Inc.||Recruiting|
|Alexandria, Virginia, United States, 22314|
|Contact: Diane Deitz firstname.lastname@example.org|
|Principal Investigator:||Diane K. Deitz, PhD||ISA Associates|