Increasing Receipt of Guideline Concordant Survivorship Care Among Black Breast Cancer Survivors Through Patient Education
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- Proportion of Eligible Participants
研究概览
简要总结
The goal of this study is to test a 6-week virtual education program among Black breast cancer survivors. The virtual program includes sessions on physical activity, goal setting, nutrition, sleep, stress, and social connections.
详细描述
This six-week feasibility study will evaluate a virtual support and education program among up to 15 Black female breast cancer survivors. Participants will be asked to attend a 90 minute group session once a week for 6 weeks and complete surveys pre and post intervention surveys to ascertain study endpoints. This study is supported by funding from Pfizer and in-kind support from the American Cancer Society, Inc.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Self-identified Black or African American race
- •Age 22-79
- •Diagnosis of Stage I, II, or III invasive breast cancer
- •Completed active treatment at least 6 months ago, but within the past five years
- •Speaks English
排除标准
- •Undergoing active treatment (i.e., surgery, chemotherapy, radiation)
- •Undergoing evaluation for suspected recurrence
研究组 & 干预措施
Breast Cancer Survivor Education Program
Participants will complete study procedures as outlined:
- 6 weekly sessions of a modified version of the PAVING the Path to Wellness education program.
干预措施: Breast Cancer Survivor Education Program (Behavioral)
结局指标
主要结局
Proportion of Eligible Participants
时间窗: 6 weeks
Defined as the number of eligible participants required to recruit required sample size.
Data collection feasibility
时间窗: 6 weeks
Proportion of participants completing evaluation surveys each at baseline and week 6.
Success Rate of Educational Intervention
时间窗: 6 weeks
Proportion of participants "very satisfied" or "completely satisfied" with intervention. Defined successful if true of 80% of participants.
Rate of Intervention Completion
时间窗: 6 weeks
Defined as the number of participants who attend at least 5 of 6 sessions.
Recruitment Retention Rate
时间窗: 6 weeks
Defined as the number of recruited participants who initiate intervention program.
Time Required to Recruit to Target
时间窗: 6 weeks
Defined as the amount of time to target accrual goal.
次要结局
- Self-Efficacy for symptom self-management(6 weeks)
- Unmet information Needs(6 weeks)
- Intention to Receive post-treatment Surveillance Mammography(6 weeks)
- Physical Activity Goal Change(6 weeks)
- Dietary Behavior Goal Change(6 weeks)
研究者
Erica T. Warner, ScD MPH
Principal Investigator
Massachusetts General Hospital