NCT00186511

Brief Summary

The major goal of this project is to test the feasibility and acceptability of using videoconferencing to provide support groups led by trained facilitators to rural women with breast cancer in northern California.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for phase_2 breast-cancer

Timeline
Completed

Started Nov 2004

Shorter than P25 for phase_2 breast-cancer

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2004

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

September 13, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 16, 2005

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2006

Completed
Last Updated

December 5, 2006

Status Verified

December 1, 2006

First QC Date

September 13, 2005

Last Update Submit

December 4, 2006

Conditions

Breast CancerStress Disorders, Post-TraumaticDepression

Outcome Measures

Primary Outcomes (2)

  • Center for Epidemiological Studies Depression Scale

  • Posttraumatic Stress Checklist

Secondary Outcomes (2)

  • Cancer Behavior Inventory

  • Courtauld Emotional Control Scale

Interventions

workbook/journal on coping with breast cancerBEHAVIORAL
supportive expressive group therapy using videoconferencingBEHAVIORAL

Eligibility Criteria

Age21 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \) has been diagnosed with breast cancer, and 2) is a woman

You may not qualify if:

  • \) under 21 years of age, and 2) does not speak and read English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Stanford, California, 94305, United States

Location

MeSH Terms

Conditions

Breast NeoplasmsStress Disorders, Post-TraumaticDepression

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesStress Disorders, TraumaticTrauma and Stressor Related DisordersMental DisordersBehavioral SymptomsBehavior

Study Officials

  • Cheryl Koopman, Ph.D.

    Stanford University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 13, 2005

First Posted

September 16, 2005

Study Start

November 1, 2004

Study Completion

June 1, 2006

Last Updated

December 5, 2006

Record last verified: 2006-12

Locations

US(1)