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Alternative Support for Rural and Isolated Women in an HMO

NCT00186212 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2011-07-01

No results posted yet for this study

Summary

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

Conditions

Interventions

BEHAVIORAL

workbook/journal on coping with breast cancer

BEHAVIORAL

standard educational materials on breast cancer

Sponsors & Collaborators

Principal Investigators

  • Cheryl Koopman, Ph.D. · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2000-09-30
Primary Completion
2002-05-31
Completion
2002-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00186212 on ClinicalTrials.gov