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OpenTrials
Completed

NCT Number: NCT00186511

Expanding Rural Access: Distance Delivery of Support

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.

Completed

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Key information

Age range

21 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Stanford University

Stanford, California, 94305, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

workbook/journal on coping with breast cancer

Behavioral

supportive expressive group therapy using videoconferencing

Behavioral

Primary outcomes

  1. Center for Epidemiological Studies Depression Scale

  2. Posttraumatic Stress Checklist

Secondary outcomes

  1. Cancer Behavior Inventory

  2. Courtauld Emotional Control Scale

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • University of California, Berkeley

Registry information

Important dates

Study start
2004
Study completion
2006
First posted
Sep 16, 2005
Registry last updated
Dec 5, 2006

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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