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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00452816
Other study ID # 06-4829-E/G 01
Secondary ID CDC Grant 1 PO1
Status Completed
Phase N/A
First received March 26, 2007
Last updated November 18, 2009
Start date April 2007
Est. completion date September 2009

Study information

Verified date November 2009
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The objective of the project is to understand how best to help mid-size employers adopt evidence-based chronic disease prevention practices that improve employee health behaviors.


Description:

Employers have the incentive and the means to play a key role in chronic disease prevention. The incentive - employers need to control the costly and growing burden of chronic diseases among their employees. The means - employers purchase 94% of private health insurance, and employees spend one third of their lives in the workplace, where they often eat, move, socialize, and smoke. Over the past 5 years, the CDC and the Task Force on Community Preventive Services have recommended a number of chronic disease prevention practices. Among these, we have identified 17 practices that employers should adopt. These practices include health insurance benefits, workplace policies, and workplace programs, and aim at increasing employees' disease screening, healthy eating, influenza immunization, physical activity and tobacco cessation. Unfortunately, employer surveys reveal low adoption of these practices.

Working with the American Cancer Society, our research team from the University of Washington has developed and pilot-tested an innovative consulting intervention to increase adoption of these practices. Our two-stage intervention is comprehensive yet tailored by employer feedback.

The intervention:

- markets the "business case" that employers can help control health-care costs and productivity losses through adoption of these practices

- enables implementation by providing tools for each practice.

In this proposal, our primary aim is to test this intervention in a randomized, controlled trial among 48 medium-sized employers with a high proportion of socioeconomically disadvantaged employees in the Puget Sound area. Our primary outcome is change in employer practices as measured by survey and validated by audit and contract and policy review.

Our secondary aims include:

- development and pilot-testing of an employee-level health risk behavior survey

- cost analysis and assessment of feasibility of our intervention

- assessment of employees' preference for different message sources and message appeals.

Our multidisciplinary research team includes business, communication, and public health faculty and has more than 10 years of experience in both chronic disease prevention and working with business. If successful, our team's approach has broad applicability to other public health problems.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date September 2009
Est. primary completion date August 2009
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Corporate size equal to 100 to 999 part-time and full-time employees (excluding seasonal and temporary workers)

- Headquarters located in King County, Washington, and in a zip code within a 30 mile radius of the research center

- Within an industry with an average annual salary below the median annual salary for King County, Washington (defined by 3-digit NAICS code)

- 50% or more employees are age 35 or older

Exclusion Criteria:

- Do not offer health insurance to full-time employees

- In existence for less than 3 years

- No physical address to which employees report

- Current or previous participation in other workplace health promotion study

- Recent refuser or non-responder for other current workplace health promotion study

- Current participant in other American Cancer Society employer program

- Not willing to be randomized to intervention or comparison group

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Workplace Solutions Consulting approach
Consulting process includes: baseline measure of best practices gap analysis and recommendations reporting delivery of "solution set" toolkits for each practice chosen for implementation
Delayed intervention
Abbreviated version of the Workplace Solutions Consulting process applied in the intervention group

Locations

Country Name City State
United States University of Washington Seattle Washington

Sponsors (3)

Lead Sponsor Collaborator
University of Washington American Cancer Society, Inc., Centers for Disease Control and Prevention

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in employer practices in health benefits, policies and programs 15 month follow-up survey No
Secondary Development and pilot-testing of an employee-level health risk behavior survey within 12 months of recruitment completion No
Secondary Cost analysis and assessment of feasibility of this intervention within 15 months of recommendations No
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