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Alternative Support for Rural and Isolated Women in an HMO

Alternative Support for Rural and Isolated Women in an HMO

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00186212
Enrollment
150
Registered
2005-09-16
Start date
2000-09-30
Completion date
2002-05-31
Last updated
2011-07-01

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

Conditions

Breast Cancer, Depression, Stress Disorders, Post-traumatic

Brief summary

Evaluate the effects of a workbook/journal for helping isolated women to cope with breast cancer.

Interventions

BEHAVIORALworkbook/journal on coping with breast cancer
BEHAVIORALstandard educational materials on breast cancer

Sponsors

University of California, Berkeley
CollaboratorOTHER
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frame
depression—
posttraumatic stress disorder—

Countries

United States

Outcome results

None listed

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