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Component and Couple Analysis of Cancer Communications

Component and Couple Analysis of Cancer Communications

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00468741
Enrollment
338
Registered
2007-05-03
Start date
2003-09-30
Completion date
2014-06-30
Last updated
2019-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast Cancer, Internet, Computer, Support, Information, Education, Control Group: Usual care and Internet access, CHESS Information Services only, CHESS Social Support & Information Services, CHESS Information, Social Support & Skills Services

Brief summary

Component and Couple Analysis of Cancer Communication CHESS, the Comprehensive Health Enhancement Support System is an innovative technology that provides information, social support and skills training to women with breast cancer. Previous CHESS clinical trials found improved patient outcomes but little is known about what services in CHESS produce those results. This study will examine whether breast cancer patient outcomes change when conceptually distinct CHESS services (information, social support, and skills training) are systematically added to a patients treatment resources. Primary Aims: * Determine the relative efficacies of different types of cancer communication treatments when they are presented alone or in combination * Determine routes or processes via which these elements work * Determine for whom the different treatment types work best.

Interventions

BEHAVIORALCHESS (Comprehensive Health Enhancement Support System)

Full CHESS for subject use

BEHAVIORALCHESS

informational services of CHESS available to subject

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Patient Quality of Lifemonthly

Secondary

MeasureTime frame
Emotional Well-beingmonthly
Self Efficacymonthly

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026