Implementing Pathways to Identify and Address Employment Concerns Among People With Cancer Across Diverse Clinical Settings
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 70
- 主要终点
- Enrollment Rate
研究概览
简要总结
The goal of this clinical trial is to learn if a clinical workflow that screens adult patients with cancer for challenges at work and refers them to supportive resources is feasible, appropriate, and acceptable to patients and staff members in 2 cancer care settings. The main questions it aims to answer are:
Is the clinical workflow feasible and acceptable to participants? Are study procedures feasible and acceptable to participants?
Patient participants will complete 2 surveys: 1 at the time of enrollment and 1 six months later.
详细描述
Investigators will conduct a prospective single-arm study at 2 sites to pilot and iteratively adapt a clinical workflow intervention, implementation strategies, and associated study procedures. Investigators will implement the clinical workflow intervention across each study site, then recruit consecutive patients (n=50) to complete patient-reported measures at 2 time points (T1: enrollment; T2: 6-month follow-up. Investigators will recruit staff members (n=20) to complete survey measures at 2 time points (T1: beginning of pilot study period; T2: end of pilot study period).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 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
- 否
入选标准
- •Eligible Patients:
- •visiting a participating medical or radiation oncology clinic for new diagnosis, treatment, or follow-up of any type of cancer;
- •employed at the time of cancer diagnosis;
- •age 18 or older;
- •able to give full informed consent;
- •able to communicate in English or Spanish.
- •Eligible Staff:
- •age 18 or older;
- •employed at one of the participating clinical sites.
排除标准
- 未提供
结局指标
主要结局
Enrollment Rate
时间窗: Baseline
T1 survey enrollment rate among eligible patients and staff
Follow-up Survey Completion Rate
时间窗: 6 months
Rate of study survey completion within 18 days of the 6-month follow-up timepoint
Staff-reported Feasibility of Intervention
时间窗: Approximately 9 months
Proportion of staff disagreeing with one or more Feasibility of Intervention Measure items
Acceptability of Intervention: Staff
时间窗: Approximately 9 months
Proportion of staff disagreeing with one or more Acceptability of Intervention Measure items
Acceptability of Intervention: Patients
时间窗: Baseline; 6 months
Proportion of patients providing negative ratings for one or more Theoretical Framework of Acceptability questionnaire items
Employment Concerns Screening
时间窗: Baseline
Proportion of eligible patients screened for employment concerns
次要结局
- Employment status(Baseline; 6 months)
- Sick leave duration(Baseline; 6 months)
- Health-related quality of life(Baseline; 6 months)
- Health insurance status(Baseline; 6 months)
- Self-efficacy(Baseline; 6 months)
- Financial toxicity(Baseline; 6 months)