This clinical trial studies whether an intervention supported by technology (blended e-health intervention) works to improve fear of progression (FOP) in women with gynecologic or breast cancer. FOP is the fear patients experience from the possibility that their cancer could grow, spread, or get worse. Managing FOP is a leading unmet concern of cancer patients. High levels of FOP are associated with distress, depression, and increased health care costs, despite this, access to resources to address FOP remain limited. The blended e-health intervention in this trial offers remote group sessions along with online sessions to help patients access the information. Session content incorporates values-based goal setting and skills practices to manage unhelpful beliefs about worry and promote helpful coping behaviors. The sessions may help patients recognize unhelpful thoughts and behaviors which reinforce worry. A blended e-health intervention may be an effective way to improve FOP in women with gynecologic or breast cancer.
Age range
18 Years
Sex
FEMALE
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A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Recruitment rate (Feasibility of enrollment)
Timeframe: Up to 18 months
Attrition rate (Intervention feasibility)
Timeframe: Up to 6 weeks
Percentage of Attendance/Sessions Completed
Timeframe: Up to 6 weeks
System Usability Scale survey (Acceptability)
Timeframe: At week 6 (T2)
Engagement measures
Timeframe: Up to 6 weeks
Themes From Open-Ended System Usability Scale Responses and Open-Ended Exit Interview Questions
Timeframe: Up to 14 months
Change in fear of progression
Timeframe: At baseline (T1), 6 weeks (T2), and 12 weeks (T3)