C-PRIME: Caregiver Protocol for Remotely Improving, Monitoring, and Extending Quality of Life
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 33
- 试验地点
- 1
- 主要终点
- Percentage of Participants Who Provide Data (Feasibility)
研究概览
简要总结
The purpose of this study is to test an intervention to improve health promoting behaviors in family caregivers of patients receiving cancer therapy
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Eligible family caregivers will be:
- •An unpaid family member or friend who provides assistance and support with healthcare of a non-institutionalized patient receiving some form of treatment for stage III or IV colorectal cancer at Moffitt Cancer Center
- •Age 18+ years
- •English or Spanish speaking
- •Able to complete questionnaires and engage in short discussions with coaches
- •Able to identify a primary care medical provider
- •Willing/able to use a mobile device provided by the study team or their own their device.
排除标准
- •Participants who do not meet the study inclusion criteria
研究组 & 干预措施
C-PRIME
Participants will wear an activity tracker for 8 weeks. During the 8 weeks of the study, participants will complete weekly survey questions about health and well-being and engage in weekly, 15-20 minute telephone/videoconference coaching sessions with a health coach.
干预措施: Remote health coaching to improve self-care behaviors (Other)
结局指标
主要结局
Percentage of Participants Who Provide Data (Feasibility)
时间窗: 12 Months
The study will be deemed feasible if at least 75% of family caregivers who participate provide data for at least 50% of study days
Percentage of Participants Who Agree to Participate (Acceptability)
时间窗: 12 Months
The study will be deemed acceptable if at least 50% of eligible family caregivers agree to participate
次要结局
- Quality of Life -Secondary Efficacy(8 Weeks)
- Self Care Behaviors - Primary Efficacy(8 Weeks)