Spiritual Care to Optimize Relationships and Experience in Adults With Acute Leukemia (SCORE Trial)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- Is it feasible to enroll patients to a spiritual intervention study?
研究概览
简要总结
This study is being done to determine if it is possible to incorporate spiritual care sessions as part of the care plan for patients hospitalized for leukemia treatment. In this study, participants will be randomly assigned to either no intervention (standard, real world inpatient spiritual care) or to receive study-specific guided spiritual sessions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 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
- 否
入选标准
- •Adults (18 years or older)
- •Diagnosis of Acute Leukemia (AML or ALL) undergoing inpatient initial therapy
- •Ability to read, understand, and speak the English language
- •Ability to understand and the willingness to sign a written informed consent document
排除标准
- •Unable to comply with spiritual care intervention
- •Relapsed or refractory acute leukemia
- •Cognitive deficits that limit participation and survey questionnaire completion
研究组 & 干预措施
Spiritual Intervention Arm
Participants receive a study specific spiritual care intervention.
干预措施: SCORE Intervention (Behavioral)
No Intervention Arm
结局指标
主要结局
Is it feasible to enroll patients to a spiritual intervention study?
时间窗: End of study (approximately 2 years)
Study will compare the number of potential participants to those that enroll and complete 3 out of 4 study intervention sessions.
Will patients accept using the study specific spiritual intervention?
时间窗: End of study (approximately 2 years)
This will be measured on using the Lothian Chaplaincy Patient Reported Outcome Measure (PROM) questionnaire. This measures patient feelings related to spiritual care using rating from not at all to all of the time.
次要结局
- Improvement on Patient Reported Spiritual Wellness(End of study (approximately 2 years))
- Improvement on Patient Reported Quality of Life(End of study (approximately 2 years))
- Improvement on Patient Reported Mood(End of study (approximately 2 years))