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| Sponsors and Collaborators: |
Park Nicollet Institute University of Minnesota |
|---|---|
| Information provided by: | Park Nicollet Institute |
| ClinicalTrials.gov Identifier: | NCT00815412 |
Purpose
A 3-year, randomized, controlled trial comparing a traditional worksite health promotion program and an activated consumer program on health practices, health status and patient activation measures.
| Condition | Intervention |
|---|---|
|
Evidence of Improved Health Status |
Behavioral: Counseling in use of health care Behavioral: Counseling in diet, exercise Other: Control |
| Study Type: | Interventional |
| Study Design: | Health Services Research, Randomized, Open Label, Active Control, Parallel Assignment |
| Official Title: | ACTIVATE: Standard Worksite Health Program vs. Activated Consumer |
| Enrollment: | 631 |
| Study Start Date: | September 2004 |
| Study Completion Date: | September 2008 |
| Primary Completion Date: | September 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Counseling in use of health care: Active Comparator | Behavioral: Counseling in use of health care |
| Counseling in diet, exercise: Active Comparator | Behavioral: Counseling in diet, exercise |
| Contol group: Placebo Comparator | Other: Control |
The design is a cluster, randomized controlled trial of two companies with three arms in each company. The arms include two control groups (one from each company), two intervention groups using a standard health promotion intervention, and two intervention groups that constitute using an activated consumer intervention. The standard intervention includes educational offerings to address health behaviors. The activated consumer intervention offers shorter education sessions and includes decision tools and skills development for working with heath care providers to better manage health and clinical conditions. Variables include health risk assessments, clinical measures such as lipids, blood pressure, body mass index, and tobacco use, perception of health care consumer practices, claims costs, and absenteeism analysis.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations More Information
| Responsible Party: | StayWell ( Paul E. Terry, PhD, President and Chief Operating Officer ) |
| Study ID Numbers: | R01 DP000104-03 |
| Study First Received: | December 29, 2008 |
| Last Updated: | December 29, 2008 |
| ClinicalTrials.gov Identifier: | NCT00815412 |
| Health Authority: | United States: Institutional Review Board |
