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
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
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
NCT ID
NCT01089699
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
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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