Electronic Health Records for Health Promotion
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Purpose
The purpose of this study is to determine whether personally controlled electronic health records can be used for health promotion in a workplace setting.
| Condition | Intervention |
|---|---|
|
Influenza |
Device: Electronic health record and messaging system |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Prevention |
| Official Title: | Health Promotion in the Workplace Using Personally Controlled Health Records |
- - Rate of influenza immunization among subjects
- Change in knowledge, attitutes, and beliefs regarding influenza and influenza immunization.
- Changes in health behaviors around influenza (e.g. hand washing and cough etiquette).
- General health outcomes related to respiratory illnesses (e.g. number of influenza-like illnesses, number of physician visits, number of missed work days).
- Rate of influenza immunization among subject household members.
| Estimated Enrollment: | 700 |
| Study Start Date: | October 2005 |
| Study Completion Date: | May 2006 |
In response to the call for research of the new Health Protection Research Initiative at the Centers for Disease Control and Prevention (CDC), we propose to adapt newly mature informatics technology to shift the paradigm for health alerting and health promotion in the workplace. The goal is to firmly ground these activities on real time information collected from and delivered to employees, in an interactive, secure, electronic environment. We will study influenza prevention and control, an archetype of public health practice requiring surveillance, communication, and timely influence of health-related behaviors. Complex information gleaned from surveillance will be processed, translated and provided to employees. The goal is to provide employees with timely, individualized health promotion messages to improve their knowledge, attitudes and beliefs regarding influenza and to increase the rate of seasonal influenza immunization for them and their household members. The approach will be evaluated in a group randomized design at several worksites of a major corporation.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- The subject is a part-time or full-time employee at a major corporation.
- The subject is eighteen years of age or older.
- The subject is comfortable reading and writing in English.
- The subject has reliable internet access at home, at school, or at work.
- The subject uses email regularly (i.e. at least once every 2 days)
- The subject does not have a known allergy to chicken eggs or a history of a severe reaction to an influenza vaccination in the past.
Exclusion Criteria:
-
Contacts and Locations| United States, Massachusetts | |
| Children's Hospital Boston | |
| Boston, Massachusetts, United States, 02116 | |
| Principal Investigator: | Kenneth D Mandl, MD, MPH | Children's Hospital Boston |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00142077 History of Changes |
| Other Study ID Numbers: | 1 R01 CDC 000065-01 |
| Study First Received: | August 31, 2005 |
| Last Updated: | April 4, 2007 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Children's Hospital Boston:
|
Influenza Electronic health record Behavior modification |
Additional relevant MeSH terms:
|
Influenza, Human Orthomyxoviridae Infections RNA Virus Infections |
Virus Diseases Respiratory Tract Infections Respiratory Tract Diseases |
ClinicalTrials.gov processed this record on May 21, 2013