search
Back to results

California WISEWOMAN Project

Primary Purpose

Cardiovascular Diseases, Chronic Diseases

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Women's health
Sponsored by
Centers for Disease Control and Prevention
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases focused on measuring CVD risk

Eligibility Criteria

40 Years - 64 Years (Adult)Female

Inclusion Criteria: National Breast and Cervical Cancer Early Detection Program (NBCCEDP)

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    September 8, 2005
    Last Updated
    February 10, 2006
    Sponsor
    Centers for Disease Control and Prevention
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00153400
    Brief Title
    California WISEWOMAN Project
    Official Title
    California WISEWOMAN Project
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2005
    Overall Recruitment Status
    Unknown status
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Centers for Disease Control and Prevention

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this trial is to provide low-income, under- or un-insured 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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cardiovascular Diseases, Chronic Diseases
    Keywords
    CVD risk

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Single
    Allocation
    Randomized

    8. Arms, Groups, and Interventions

    Intervention Type
    Behavioral
    Intervention Name(s)
    Women's health

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    64 Years
    Eligibility Criteria
    Inclusion Criteria: National Breast and Cervical Cancer Early Detection Program (NBCCEDP)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Julie Will
    Organizational Affiliation
    Centers for Disease Control and Prevention
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    California WISEWOMAN Project

    We'll reach out to this number within 24 hrs