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临床试验/NCT07408310
NCT07408310招募中不适用

Trial of Spiritual Care Interventions for Patients With Cancer

Weill Medical College of Cornell University3 个研究点 分布在 1 个国家目标入组 288 人开始时间: 2026年3月24日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
288
试验地点
3
主要终点
Patients' spiritual wellness as assessed by measures of spiritual well-being

研究概览

简要总结

This study aims to determine the effects of 2 spiritual care interventions. Spiritual wellness and healthcare service utilization will be measured from a sample of advanced cancer patients recruited from outpatient settings.

详细描述

This study is a stratified permuted-block RCT to determine the effects of 2 spiritual care interventions on advanced cancer patients' spiritual wellness (i.e., spiritual well-being and satisfaction of spiritual care needs) and specific forms of healthcare service utilization (i.e., hospice enrollment and ICU admissions) in a sample of advanced cancer patients (N=288) recruited from outpatient settings. Patients will be assigned to "Spiritual Care Intervention #1" (active 1), "Spiritual Care Intervention #2" (active 2), or "Spiritual Care Intervention #3" (control) arm of the trial (overall ratio 1:1:1) using permuted-block randomization within strata defined by geographic location (NYC, Houston Metro Area) and recruitment site (NYC: BMH; Houston Metro Area: UTMB, MDACC). Spiritual care intervention details are being withheld until the trial concludes to protect the scientific integrity of the study. Only 1 of the 2 active interventions will be administered at each site at a given time to avoid within-site cross-contamination between the 2 active intervention arms of the trial.

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
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

The participant's oncologist is the care provider who is masked. This masking is needed to ensure the scientific integrity of the trial.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with an advanced cancer.
  • Member of a religious faith community organization.
  • Fluent in English.

排除标准

  • Received spiritual care from a healthcare chaplain within the past 2 months.
  • Too weak or cognitively impaired to engage in study activities.

研究组 & 干预措施

Spiritual Care Intervention #1

Experimental

This is an experimental condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.

干预措施: Spiritual Care Intervention #1 (Behavioral)

Spiritual Care Intervention #2

Experimental

This is also an experimental condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.

干预措施: Spiritual Care Intervention #2 (Behavioral)

Spiritual Care Intervention #3

Active Comparator

This is the active comparator condition arm. Intervention details are being withheld until the trial concludes to protect the scientific integrity of the study.

干预措施: Spiritual Care Intervention #3 (Behavioral)

结局指标

主要结局

Patients' spiritual wellness as assessed by measures of spiritual well-being

时间窗: 2 months

The spiritual well-being outcome measure for this trial is the total score for the 12-item Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being Scale \[FACIT-Sp-12\], which has a range from 0 to 48. The higher the score, the greater the spiritual well-being.

Participants' number of hospice enrollments

时间窗: up to 12 months

Number of hospice enrollments over time, up to 12 months.

Participants' number of ICU admissions

时间窗: up to 12 months

Number of ICU admissions over time, up to 12 months.

Patients' spiritual wellness as assessed by measures of satisfaction of spiritual care needs.

时间窗: 2 months

The satisfaction of spiritual care needs outcome measure for this trial is a reverse-coded total score for the 13-item Spiritual Needs Assessment for Patients \[SNAP\], which measures unmet spiritual care needs and has a range from 13 to 52. The higher the reverse-coded score, the greater the satisfaction of spiritual care needs.

次要结局

  • Patients' quality of life(2 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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