Expanding Rural Access: Distance Delivery of Support
Primary Purpose
Breast Cancer, Stress Disorders, Post-Traumatic, Depression
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
workbook/journal on coping with breast cancer
supportive expressive group therapy using videoconferencing
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria: 1) has been diagnosed with breast cancer, and 2) is a woman Exclusion Criteria: 1) under 21 years of age, and 2) does not speak and read English
Sites / Locations
- Stanford University
Outcomes
Primary Outcome Measures
Center for Epidemiological Studies Depression Scale
Posttraumatic Stress Checklist
Secondary Outcome Measures
Cancer Behavior Inventory
Courtauld Emotional Control Scale
Full Information
NCT ID
NCT00186511
First Posted
September 13, 2005
Last Updated
December 4, 2006
Sponsor
Stanford University
Collaborators
University of California, Berkeley
1. Study Identification
Unique Protocol Identification Number
NCT00186511
Brief Title
Expanding Rural Access: Distance Delivery of Support
Official Title
Expanding Rural Access: Distance Delivery of Support
Study Type
Interventional
2. Study Status
Record Verification Date
December 2006
Overall Recruitment Status
Completed
Study Start Date
November 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Stanford University
Collaborators
University of California, Berkeley
4. Oversight
5. Study Description
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.
Detailed Description
Women with breast cancer in rural areas are likely exhaust their usual sources of psychosocial support while still facing challenges posed by breast cancer, but are unlikely to have access to professionally-led support groups. In this community-based project, we assessed the feasibility and acceptability of providing support groups to women with breast cancer in a large rural area using videoconferencing and a workbook journal, and we assessed the intervention's potential to reduce distress and increase emotional expression and self-efficacy for coping with cancer. Twenty-seven women in the Intermountain Region of northeastern California participated in 8-session support groups led by an oncology social worker by going to nearby videoconferencing sites. Feasibility and acceptability were demonstrated. Older as well as younger women were comfortable using videoconferencing and said the groups were valuable because they promoted information sharing and emotional bonds with other women with breast cancer. They emphasized the importance of a professional facilitator and identified advantages of using videoconferencing for support groups. Pretest and posttest comparisons showed significant decreases in depression and posttraumatic stress disorder symptoms. The results suggest that the intervention has the potential to provide a valuable service that is not readily available in rural communities.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Stress Disorders, Post-Traumatic, Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
workbook/journal on coping with breast cancer
Intervention Type
Behavioral
Intervention Name(s)
supportive expressive group therapy using videoconferencing
Primary Outcome Measure Information:
Title
Center for Epidemiological Studies Depression Scale
Title
Posttraumatic Stress Checklist
Secondary Outcome Measure Information:
Title
Cancer Behavior Inventory
Title
Courtauld Emotional Control Scale
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1) has been diagnosed with breast cancer, and 2) is a woman
Exclusion Criteria:
1) under 21 years of age, and 2) does not speak and read English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cheryl Koopman, Ph.D.
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Expanding Rural Access: Distance Delivery of Support
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