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A Trial Testing Professional and Peer-led Support Online Support Groups for Young Canadian Breast Cancer Survivors (CBCRA09)

Primary Purpose

Breast Cancer

Status
Unknown status
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
online support group
online support group
home study support materials
Sponsored by
British Columbia Cancer Agency
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring breast cancer, support groups, Primary diagnosis of breast cancer within the past three years.

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • less than 46 years old with primary breast cancer

Exclusion Criteria:

  • older than 45 and in active treatment

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Arm Label

    Professionally-led online support

    Peer-led online support

    self-study materials

    Arm Description

    Members assigned to 10-week online support group with a professional counsellor.

    Outcomes

    Primary Outcome Measures

    Reduced anxiety
    Psychological assessment measures given immediately following the 12 week group, and at 6 months and 12 months follow-up, will determine if one or both of the study groups effectively improve quality of life, reduce distress, and enhance self-efficacy and life satisfaction for young breast cancer survivors. Additionally, tests will be performed to investigate whether discussing emotional matters predicts greater improvements.

    Secondary Outcome Measures

    Full Information

    First Posted
    March 17, 2010
    Last Updated
    March 17, 2010
    Sponsor
    British Columbia Cancer Agency
    Collaborators
    University of Calgary, McMaster University, University of British Columbia, Tom Baker Cancer Centre, CancerCare Manitoba
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01089699
    Brief Title
    A Trial Testing Professional and Peer-led Support Online Support Groups for Young Canadian Breast Cancer Survivors
    Acronym
    CBCRA09
    Official Title
    A Randomized Control Trial Testing the Efficacy of Professional and Peer-Led Online Support Groups for Young Canadian Breast Cancer Survivors
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2009
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 2010 (undefined)
    Primary Completion Date
    March 2013 (Anticipated)
    Study Completion Date
    March 2015 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    British Columbia Cancer Agency
    Collaborators
    University of Calgary, McMaster University, University of British Columbia, Tom Baker Cancer Centre, CancerCare Manitoba

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Young women who have finished treatment for breast cancer regularly report a lack of psychological and social support in their lives. They often continue to struggle with survivorship issues such as ongoing distress and the challenge of how to rebuild their lives after treatment. This experiment will compare two online support group (OSG) options to determine if both forms of support help young breast cancer survivors adjust, by reducing treatment-related intrusions and helping women re-engage in valued activities and commitments. It will also test if these 2 types of OSG's help womens' mood, feelings of loneliness, confidence, and overall life satisfaction. It will explore the processes within support groups that help to create positive change for young women after cancer treatment. Previous work by this team in a smaller study has shown that online support groups led by professional counselors can be carried out over the Internet, and that they produce helpful benefits for young women survivors of breast cancer. The online groups were comprised of 10 sessions of real time chats, with each session focused on a specific topic. Participants were provided with an educational manual designed to improve skills for coping after cancer, and they were instructed to read one chapter a week in preparation for the chats. The women enjoyed the groups and 3 months after completing the groups, they reported improved quality of life, lower emotional distress, and enhanced coping. However, a large study to determine the strength and reliability of these early promising findings is needed. The questions to be examined are whether trained peers (other young breast cancer survivors) might be able to facilitate the online groups and provide similar positive benefits for young breast cancer survivors, and what facilitators can do to maximize positive benefits in online support groups. This is a multi-provincial, 3-arm study that will compare a professionally-led OSG (with an educational manual) and a peer-led OSG (with an education manual) with a group that just receives the educational manual. Psychological assessment measures given immediately following the 12 week group, and at 6 months and 12 months follow-up, will determine if one or both of the study groups effectively improve quality of life, reduce distress, and enhance self-efficacy and life satisfaction for young breast cancer survivors. Additionally, tests will be performed to investigate whether discussing emotional matters predicts greater improvements.
    Detailed Description
    Problem to be investigated: Innovative psychosocial interventions that enhance quality of life as quickly and fully as possible are needed. The psychosocial burden of breast cancer treatments and their sequelae are especially high for younger women (45 years and younger) who are more likely to experience aggressive disease, multi-modal treatments, and higher mortality rates. Psychosocial interventions that can assist women in their return to valued activities and reduce suffering are urgently needed. Illness intrusiveness is a construct and a measure describing the degree to which disease and treatments interfere and disrupt important activities and commitments, and is a key component of quality of life. In previous work, we demonstrated that an internet-delivered psychosocial intervention appeared to reduce illness intrusiveness and distress at follow-up in preliminary pilot data. Professional-led internet-delivered psychosocial interventions are showing promise but there is a need to test efficacy, as well as to develop and test other, less costly interventions that can be utilized by this and other cancer populations. Objectives: To test the efficacy of a 12- week Professional-led Online Support Group plus Education (OSG+E) and a Peer-led OSG+E compared to an Education-alone (E) intervention for reducing illness intrusiveness in young breast cancer survivors, and to test a primary mediator, emotional processing. Secondary objectives are to test additional outcomes, specifically, emotional distress, emotional support, loneliness, self-efficacy and life satisfaction. A third objective is to explore the role of two potential mediators of outcome, emotional suppression and social constraint. Methodology: A 3-arm randomized controlled trial will be employed among Canadian women 45 years of age and younger (N =210 ) who have completed primary treatment for breast cancer. Measures of Illness Intrusiveness, Distress, Life Satisfaction, Self-efficacy, Loneliness and Perceived Support will be collected at baseline, completion of treatment (3 months) and at 6 and 12 months. A form of random regression modeling will be used to create individual slopes to test the primary hypotheses, while multiple regression analyses, based on the MacArthur Model, will test the role of mediators. Significance of the research to breast cancer: Women with breast cancer are using the internet for information gathering and support, and this study will determine the efficacy of two forms of internet-delivered interventions (Professional and Peer) for enhancing the adjustment process after primary treatment is completed. Understanding of mediators will inform understanding of how to enhance efficacy of the 2 models of OSG's. The results will be of value to women with breast cancer as well as health care and community-based supportive care organizations.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Cancer
    Keywords
    breast cancer, support groups, Primary diagnosis of breast cancer within the past three years.

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    210 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Professionally-led online support
    Arm Type
    Active Comparator
    Arm Description
    Members assigned to 10-week online support group with a professional counsellor.
    Arm Title
    Peer-led online support
    Arm Type
    Active Comparator
    Arm Title
    self-study materials
    Arm Type
    Active Comparator
    Intervention Type
    Behavioral
    Intervention Name(s)
    online support group
    Other Intervention Name(s)
    Professionally led online support group.
    Intervention Description
    online support group
    Intervention Type
    Behavioral
    Intervention Name(s)
    online support group
    Intervention Description
    online support group
    Intervention Type
    Behavioral
    Intervention Name(s)
    home study support materials
    Other Intervention Name(s)
    self-study materials
    Intervention Description
    self-study materials
    Primary Outcome Measure Information:
    Title
    Reduced anxiety
    Description
    Psychological assessment measures given immediately following the 12 week group, and at 6 months and 12 months follow-up, will determine if one or both of the study groups effectively improve quality of life, reduce distress, and enhance self-efficacy and life satisfaction for young breast cancer survivors. Additionally, tests will be performed to investigate whether discussing emotional matters predicts greater improvements.
    Time Frame
    1 year

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    45 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: less than 46 years old with primary breast cancer Exclusion Criteria: older than 45 and in active treatment
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Kate MacGregor, MPH
    Phone
    604-707-5900
    Ext
    4955
    First Name & Middle Initial & Last Name or Official Title & Degree
    Joanne Stephen, Ph.D.
    Phone
    604-707-5900
    Ext
    4960

    12. IPD Sharing Statement

    Learn more about this trial

    A Trial Testing Professional and Peer-led Support Online Support Groups for Young Canadian Breast Cancer Survivors

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