Iowa WISEWOMAN Project

This study has been completed.
Sponsor:
Information provided by:
Centers for Disease Control and Prevention
ClinicalTrials.gov Identifier:
NCT00153374
First received: September 8, 2005
Last updated: March 13, 2012
Last verified: March 2012
  Purpose

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 Intervention
CVD Risk
Behavioral: Women's health

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Prevention
Official Title: Iowa WISEWOMAN Project

Further study details as provided by Centers for Disease Control and Prevention:

  Eligibility

Ages Eligible for Study:   40 Years to 64 Years
Genders Eligible for Study:   Female
Criteria

Inclusion Criteria:

  • NBCCEDP

Exclusion Criteria:

-

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00153374

Sponsors and Collaborators
Investigators
Study Chair: Julie Will Centers for Disease Control and Prevention
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00153374     History of Changes
Other Study ID Numbers: CDC-NCCDPHP-3566, U57/CCU719169-02
Study First Received: September 8, 2005
Last Updated: March 13, 2012
Health Authority: United States: Federal Government

ClinicalTrials.gov processed this record on September 22, 2014