MedPath

Expanding Rural Access: Distance Delivery of Support

Phase 2
Completed
Conditions
Breast Cancer
Stress Disorders, Post-Traumatic
Depression
Registration Number
NCT00186511
Lead Sponsor
Stanford University
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
40
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Center for Epidemiological Studies Depression Scale
Posttraumatic Stress Checklist
Secondary Outcome Measures
NameTimeMethod
Cancer Behavior Inventory
Courtauld Emotional Control Scale

Trial Locations

Locations (1)

Stanford University

🇺🇸

Stanford, California, United States

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