Effectiveness of the CHESS eHealth Cancer Support Intervention in Population-based Care

November 14, 2019 updated by: University of Wisconsin, Madison

Using Technology to Enhance Cancer Communication and Improve Clinical Outcome: Effectiveness of the CHESS Ehealth Cancer Support Intervention in Population-Based Care Study

The study's aim is to provide information about the clinical and business cases for comprehensive interactive cancer communication systems (ICCS) in the context of real world use for cancer care.

This study will be conducted within the Kaiser Permanente Northwest (KPNW) healthcare system. Outcomes for this study include amount of ICCS use and women's ratings of cancer information competence, perceived social support, and emotional well being. Secondary outcomes will include healthcare utilization, cost-effectiveness, and clinician ratings of healthcare visits.

Study Overview

Study Type

Interventional

Enrollment (Actual)

368

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Oregon
      • Portland, Oregon, United States, 97227
        • Kaiser Permanente Northwest

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • All subjects must be within 2 months of their primary breast cancer diagnosis,
  • All subjects must be at least 18 years of age

Exclusion Criteria:

  • Illiterate
  • Homeless

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Usual Care
A group using a Basic ICCS provided by KPNW
Experimental: Intervention
A group using an enhanced ICCS with KPNW web resources and the Comprehensive Health Enhancement Support System (CHESS.)

Half of the participating women will be randomly assigned to use an informative but static website (Basic ICCS), and half will be offered a fully interactive CHESS (Enhanced ICCS + the Basic ICCS). Study outcome data will be gathered from patients, clinicians, and the healthcare system (i.e., from the electronic medical record: EMR) for at least 8 months after study entry. We propose that the Enhanced ICCS relative to the Basic ICCS, will:

  • Improve patients' sense of cancer information competence (perceived ability to obtain and use relevant information)
  • Reduce patients' negative affect and increase their emotional well being
  • Improve patients' sense of social support
  • Improve patients' health self-efficacy
  • Improve patients' ratings of experience with cancer specialty care services
  • Improve patients' health related quality of life (HRQL)
  • Improve clinicians' ratings of quality of patient contacts
  • Reduce healthcare utilization and costs (obtained via the EMR)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Amount of ICCS use and women's ratings of cancer information competence, perceived social support, and emotional well being. Secondary outcomes will include healthcare utilization, cost-effectiveness, and clinician ratings of healthcare visits.
Time Frame: 12 Months
12 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Timothy Baker, University of Wisconsin, Madison

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2009

Primary Completion (Actual)

August 1, 2013

Study Completion (Actual)

August 1, 2013

Study Registration Dates

First Submitted

December 14, 2009

First Submitted That Met QC Criteria

December 15, 2009

First Posted (Estimate)

December 16, 2009

Study Record Updates

Last Update Posted (Actual)

November 18, 2019

Last Update Submitted That Met QC Criteria

November 14, 2019

Last Verified

February 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • H-2008-0222
  • SMPH/MEDICINE/MEDICINE*G (Other Identifier: UW Madison)
  • A534253 (Other Identifier: UW- Madison)
  • 5P50CA095817 (U.S. NIH Grant/Contract)
  • XP08323 (Other Identifier: University of Wisconsin Carbone Cancer Center)
  • NCI-2013-01101 (Registry Identifier: NCI Trial ID)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Primary Breast Cancer

Clinical Trials on Enhanced ICCS with KPNW web resources and the Comprehensive Health Enhancement Support System (CHESS.)

  • University of Wisconsin, Madison
    National Cancer Institute (NCI)
    Completed
    CHESS and Cancer Mentor | CHESS Only | Mentor Only | Control (Internet Only)
    United States
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