A Novel Prosocial Online Support Group for Distressed Breast Cancer Survivors
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Breast Neoplasms
- Sponsor
- Temple University
- Enrollment
- 184
- Locations
- 1
- Primary Endpoint
- Hospital Anxiety and Depression Scale
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
The investigators hypothesize that breast cancer survivors participating in a prosocial online support group will have a significantly lower mean level of psychological symptoms (anxiety/depression) and higher mean level of sense of purpose post-intervention than participants in a standard online support group.
Detailed Description
Psychological distress is a significant problem among breast cancer survivors. Many survivors turn to the internet for information and support, yet few controlled studies have examined the effectiveness and safety of online support groups. The investigators are testing the potential efficacy, acceptability, and feasibility of an innovative theory-based online support group (OSG) for breast cancer survivors. Members of the control group will participate in a standard OSG that encourages self-expression. Members of the experimental condition will participate in a prosocial OSG that provides structured helping opportunities and coaching on how best to give support to others. Participants will complete two telephone interviews and six weekly online support group meetings.
Investigators
Eligibility Criteria
Inclusion Criteria
- •diagnosed with stage I or II breast cancer in preceding 36 months
- •21-64 years of age
- •access to and ability to use a computer and the internet to communicate with others
- •fluent in spoken English
- •meet the screening criteria for psychological distress (score \>7 on either the depression or anxiety subscale of the Hospital Anxiety and Depression Scales
Exclusion Criteria
- •currently taking medication for depression
Outcomes
Primary Outcomes
Hospital Anxiety and Depression Scale
Time Frame: change from baseline to one month post-intervention
Secondary Outcomes
- Sense of Coherence measure(change from baseline to one month post-intervention)