Navigator Guided e-Psychoeducational Intervention for Prostate Cancer Patients and Their Caregivers
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 391
- 试验地点
- 1
- 主要终点
- Final Survey Results per Study Arm
研究概览
简要总结
The purpose of this study is to evaluate the impact of providing newly diagnosed prostate cancer patients and their caregivers with an interactive mobile tablet technology-based application delivered by a community navigator versus providing National Cancer Institute (NCI) information booklets delivered by a Community Navigator (CN) on patient outcomes (decisional satisfaction, quality of life, knowledge, decisional conflict) and shared decision making practices (decision making involvement).
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 40 Years 至 80 Years（Adult, Older Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Men newly diagnosed (within 6 months) with biopsy confirmed case of prostate cancer
- •40 - 80 years of age
- •Able to speak and read English
- •Live within 120 miles of a healthcare treatment facility
- •Have no documented or observable visual, auditory, psychiatric, or neurological disorders that would interfere with study participation
- •Be able to complete telephone interviews
- •Have not completed the first course of treatment
- •Have a family member/caregiver willing to participate
- •Capable of providing written consent for study participation. Men diagnosed with early stage, locally advanced or metastatic disease or men who are on active surveillance will be eligible to participate in this study.
- •Caregiver must be aged 18 or older
- •Caregiver must be identified by patient as their caregiver (i.e., provider of emotional and/or physical care)
- •Caregiver must have not been diagnosed with cancer in the previous year or be receiving cancer treatment
排除标准
- 未提供
结局指标
主要结局
Final Survey Results per Study Arm
时间窗: 6 months post baseline survey
Investigators plan to assess if the psycho-educational intervention, PHIN, delivered by a CN is more efficacious as compared to NCI Information Booklets (IB) delivered by a CN. Participants will be asked to complete a baseline set of surveys and follow-up surveys at three additional time points: (1) 6 weeks after receiving the educational intervention; (2) after the follow-up decision with their doctor or health care provider; and (3) 6 months after the baseline surveys were done.
次要结局
未报告次要终点