Trial Information
Alternative Support for Rural and Isolated Women in an HMO
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
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
depression
Principal Investigator
Cheryl Koopman, Ph.D.
Investigator Role:
Principal Investigator
Investigator Affiliation:
Stanford University
Authority:
United States: Institutional Review Board
Study ID:
5BB-1801
NCT ID:
NCT00186212
Start Date:
September 2000
Completion Date:
May 2002
Related Keywords:
- Stress Disorders, Post-traumatic
- Depression
- Breast Cancer
- Breast Neoplasms
- Depression
- Depressive Disorder
- Stress Disorders, Post-Traumatic
- Stress Disorders, Traumatic
Name | Location |
Stanford University |
Stanford, California 94305 |