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Mentor Integration Study

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00468468
First Posted: May 2, 2007
Last Update Posted: February 5, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
University of Wisconsin, Madison
April 30, 2007
May 2, 2007
February 5, 2016
September 2003
September 2008   (Final data collection date for primary outcome measure)
Patient quality of life [ Time Frame: throughout study ]
Patient quality of life
Complete list of historical versions of study NCT00468468 on ClinicalTrials.gov Archive Site
  • Self efficacy [ Time Frame: throughout study ]
  • Emotional well being [ Time Frame: throughout study ]
  • Self efficacy
  • Emotional well being
Not Provided
Not Provided
 
Mentor Integration Study
Mentor Integration Study

Mentor Integration Project

This study will investigate the benefits of CHESS, a Human Cancer Mentor and the potential additional benefit of combining CHESS and a Cancer Mentor compared to Internet access for women diagnosed with breast cancer. Our goal is to advance interactive cancer communication systems, thus improving quality of life for patients and families facing cancer, especially underserved populations.

Primary Aims:

  • Determine if the Internet, CHESS, a Cancer Mentor, or a combination of CHESS and the Cancer Mentor improve quality of life for women with breast cancer
  • Determine which of the above conditions is most effective
  • Determine which of the above conditions is most cost efficient
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
  • CHESS and Cancer Mentor
  • CHESS Only
  • Mentor Only
  • Control (Internet Only)
Behavioral: CHESS (Comprehensive Health Enhancement Support System) and Human Cancer Mentor
computer based education and support
  • Experimental: CHESS Condition
    Subjects who receive the CHESS (Comprehensive Health Enhancement Support System)
    Intervention: Behavioral: CHESS (Comprehensive Health Enhancement Support System) and Human Cancer Mentor
  • Experimental: Mentor Condition
    Subjects who receive access to a Human Cancer Mentor only
    Intervention: Behavioral: CHESS (Comprehensive Health Enhancement Support System) and Human Cancer Mentor
  • Experimental: CHESS + Mentor
    Subjects who receive the CHESS system plus a Human Cancer Mentor
    Intervention: Behavioral: CHESS (Comprehensive Health Enhancement Support System) and Human Cancer Mentor
  • No Intervention: Internet Only
    Subjects receive routine care and nothing else
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
126
September 2008
September 2008   (Final data collection date for primary outcome measure)

Inclusion Criteria:

Eligibility for this protocol is as follows:

  • All subjects must be within 2 months of their primary breast cancer diagnosis,
  • All subjects must be at least 18 years of age,
  • All subjects must be able to read and write English at the 6th-grade level
  • Not homeless
Sexes Eligible for Study: Female
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00468468
2003-192
1P50CA09817-01A1
Not Provided
Not Provided
Not Provided
University of Wisconsin, Madison
University of Wisconsin, Madison
National Cancer Institute (NCI)
Principal Investigator: Robert Hawkins, PhD. University of Wisconsin, Madison
University of Wisconsin, Madison
February 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP