West Virginia WISEWOMAN Project

Sponsor
West Virginia University (Other)
Overall Status
Completed
CT.gov ID
NCT00153426
Collaborator
(none)
733
1
56

Study Details

Study Description

Brief Summary

To provide low-income, under- or uninsured 40- to 64-year-old women with the knowledge, skills, and opportunities to improve diet, physical activity, and other lifestyle behaviors to prevent, delay and control cardiovascular and other chronic diseases.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: West Virginia WISEWOMAN
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
733 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
West Virginia WISEWOMAN Project
Study Start Date :
Jul 1, 2003
Actual Primary Completion Date :
Mar 1, 2008
Actual Study Completion Date :
Mar 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Experimental: lifestyle counseling

Women assigned to lifestyle change intervention arm for nutrition and physical activity with print-based tailored health communications and a computer-based interactive nutrition program targeting health behaviors of diet and physical activity. Women in a control group did not receive the intervention.

Behavioral: West Virginia WISEWOMAN
Print-based tailored health communications and computer-based interactive nutrition program

Outcome Measures

Primary Outcome Measures

  1. change in physical activity and nutrition lifestyle behaviors [baseline and one year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 64 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • NBCCEDP
Exclusion Criteria:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • West Virginia University

Investigators

  • Study Chair: Julie Will, Centers for Disease Control and Prevention

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Robin Seabury, Associate Director, West Virginia University
ClinicalTrials.gov Identifier:
NCT00153426
Other Study ID Numbers:
  • CDC-NCCDPHP-4234
  • U58/CCU322798-01
First Posted:
Sep 12, 2005
Last Update Posted:
Jun 28, 2012
Last Verified:
Jun 1, 2012

Study Results

No Results Posted as of Jun 28, 2012