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OpenTrials
Completed

NCT Number: NCT01108016

Expanding Rural Access: Distance Delivery of Support Groups (Main Study)

The study will answer two questions about women with breast cancer in rural communities:

1. Will they find this support group format utilizing videoconferencing acceptable and rewarding? 2. Will they report a greater sense of emotional and informational support, and less depression and traumatic stress, than the control groups of women who wait to participate until after the first groups have ended?

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Key information

Age range

21 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Stanford University School of Medicine

Stanford, California, 94305, United States

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

To be eligible to participate, a woman must meet all of the following criteria:

  • be a resident of one of nine rural counties in northeastern California (Modoc, Plumas, Siskiyou, Shasta, Lassen, Trinity, Sierra, Nevada, and Tehama),
  • be able to travel to a rural health facility included in the Northern Sierra Rural Health Network to participate in videoconferencing meetings;
  • be able to speak and read English well enough to be able to read, discuss, and comprehend the consent form;
  • be 21 years of age or older;
  • have been diagnosed with breast cancer by a physician; and
  • who (in the judgment of the Local Coordinator) is not unduly distressed or otherwise not able to participate effectively in a support group.

Women will be included with any stage of breast cancer as our pilot study demonstrated that in these rural communities, women wanted to include women with any stage of breast cancer in their groups. Also, our pilot study results showed that it worked fine to include women regardless of the period elapsing since they received their diagnosis, as our pilot study results showed that some women with a long period of time elapsing since receiving their diagnosis were still in need of a source of social support for coping with having had this experience and felt that they had a lot of help to offer women who had more recently received a breast cancer diagnosis. The 9 counties were selected because they are among the most remote counties in California, yet they have strong primary care systems in place, and most patients receive specialty care in-state, as opposed to out-of-state. Every effort will be made to include women of ethnic minority groups.

The support group facilitator, community advisory board (CAB) members, and the local community coordinators will also be recruited for the interviews, with informed consent, identified by having played one of these roles for this study.

Exclusion criteria

Potential participants who do not meet all of the inclusion criteria listed above will be excluded.

Treatment and study plan

Videoconferencing support group

Behavioral

Primary outcomes

  1. Intensity and frequency of posttraumatic stress symptoms in the past month as assessed by total score on the Posttraumatic Check List - Specific version (PCL-S) for breast cancer.

    Time frame: after 8 weeks of the immediate group sessions

  2. Intensity and frequency of depression symptoms in the past week as assessed by total score on the Center for Epidemiological Studies Depression scale (CES-D)

    Time frame: after 8 weeks of the immediate group sessions

Secondary outcomes

  1. Intensity and frequency of emotional control as assessed by the total score on the Courtauld Emotional Control Scale (CECS),

    Time frame: after 8 weeks of the immediate group sessions

  2. Level of self-efficacy for coping with breast cancer as assessed by the total score on the Cancer Behavior Inventory (CBI).

    Time frame: after 8 weeks of the immediate group sessions

  3. Satisfaction with social support as assessed by the total satisfaction score on the UCLA Social Support Inventory.

    Time frame: after 8 weeks of the immediate group sessions

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • California Breast Cancer Research Program

Registry information

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Apr 21, 2010
Registry last updated
Dec 6, 2010

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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