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临床试验/NCT04106089
NCT04106089已完成不适用

Sleep in Pediatric Hematopoietic Stem Cell Transplant Patients

Children's Hospital of Philadelphia2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年11月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Patient Acceptability Questionnaire

研究概览

简要总结

Through an aggregated N=1 randomized controlled design (each patient will serve as their own control, with the 5-day intervention period determined by randomization), the current study will test the acceptability, feasibility, and impact on sleep and supportive care engagement of protecting one 6-hour window for nighttime sleep (intervention) relative to regular vitals checks (observation only periods) during Hematopoietic Stem Cell Transplant (HSCT) recovery.

详细描述

Context: Patients undergoing treatment for cancer face disease, treatment, and environmental obstacles to sufficient, sound sleep. Hospitalizations can further worsen sleep quality and quantity due to overnight vitals checks, medication administration, blood draws, and environmental noise and light. For patients undergoing hematopoietic stem cell transplant (HSCT), the risk for poor sleep is especially high due to protracted hospitalization, frequent vitals checks resulting in multiple night awakenings, and high symptom burden peaking approximately 10 days post-transplant.

Objectives:

Primary: Test the acceptability and feasibility of protecting one 6-hour window for nighttime sleep (intervention) relative to regular vitals checks (observation only periods) during HSCT recovery.

Secondary: Assess the effect of one 6-hour window for nighttime sleep on subject sleep and engagement in supportive care on the oncology unit.

Study Design:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

盲法说明

actigraphy scoring will be conducted by study staff blind to patient study arm

入排标准

年龄范围
8 Years 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Males or females age 8 to 21 years.
  • Undergoing HSCT at The Children's Hospital of Philadelphia
  • Parent/guardian permission (informed consent) and if appropriate, child assent.

排除标准

  • History of developmental delays given the relationship to sleep/wake patterns
  • Sleep disorder diagnosis as documented in the medical record
  • Cognitive delays that impact the ability to complete study measures
  • Not proficient in English

结局指标

主要结局

Patient Acceptability Questionnaire

时间窗: 15 days after transplant

Brief questionnaire created for this study evaluating the patient's acceptability of adjusting vitals checks. Participants reported agreement with each statement on a 5-point likert scale from not at all (1) to extremely (5). Higher values indicate greater agreement.

Parent Acceptability Questionnaire

时间窗: 15 days after transplant

Brief questionnaire created for this study evaluating the patient's acceptability of adjusting vitals checks. Participants reported agreement with each statement on a 5-point likert scale from not at all (1) to extremely (5). Higher values indicate greater agreement.

Nurse Acceptability Questionnaire

时间窗: 15 days after transplant

Brief questionnaire created for this study evaluating the nurse's acceptability of adjusting vitals checks. Nurses reported agreement with each statement on a 5-point likert scale from not at all (1) to extremely (5). Higher values indicate greater agreement.

Health-related Quality of Life (HRQL)

时间窗: 15 days after transplant

Using the Pediatric Quality of Life Inventory - Stem Cell Transplant (SCT) module. Scale values range from 0 to 100, with higher scores indicating better functioning.

次要结局

  • Actigraphy Sleep Efficiency(Day of the transplant through 15 days after the transplant)
  • Actigraphy Total Sleep Time(Day of the transplant through 15 days after the transplant)
  • Actigraphy Awakenings-minutes Per Day(Day of the transplant through 15 days after the transplant)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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