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Alternative Support for Rural and Isolated Women in an HMO

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00186212
First Posted: September 16, 2005
Last Update Posted: July 1, 2011
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:
University of California, Berkeley
Information provided by:
Stanford University
September 13, 2005
September 16, 2005
July 1, 2011
September 2000
May 2002   (Final data collection date for primary outcome measure)
  • depression
  • posttraumatic stress disorder
Same as current
Complete list of historical versions of study NCT00186212 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Alternative Support for Rural and Isolated Women in an HMO
Alternative Support for Rural and Isolated Women in an HMO
Evaluate the effects of a workbook/journal for helping isolated women to cope with breast cancer.
Not Provided
Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Stress Disorders, Post-traumatic
  • Depression
  • Breast Cancer
  • Behavioral: workbook/journal on coping with breast cancer
  • Behavioral: standard educational materials on breast cancer
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
150
May 2002
May 2002   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 1) is a woman; and 2) has been diagnosed with primary breast cancer

Exclusion Criteria:

  • 1) is under 18; or 2) can not speak and read in English
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
 
 
NCT00186212
5BB-1801
No
Not Provided
Not Provided
Cheryl Koopman, Ph.D., Professor (Research), Stanford University
Stanford University
University of California, Berkeley
Principal Investigator: Cheryl Koopman, Ph.D. Stanford University
Stanford University
June 2011

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