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临床试验/NCT03946865
NCT03946865撤回不适用

Reiki Therapy - an Intervention in Hematology/Oncology Cancer Patients Hospitalized in an Inpatient Setting - a Pilot Study.

Mayo Clinic2 个研究点 分布在 1 个国家开始时间: 2019年7月10日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
Mayo Clinic
试验地点
2
主要终点
Change in anxiety symptoms

研究概览

简要总结

Researchers are trying to determine if offering and providing reiki therapy in hospitalized hematology/oncology cancer subjects has any effects on symptoms and feeling during the subjects hospital stay.

详细描述

Primary Aim:

The primary aim of this study is to evaluate the feasibility of offering and providing Reiki Therapy in hospitalized hematology/oncology cancer patients. The intervention should not - interfere with the medical management of the participants. The investigators hypothesize that Reiki Sessions will be successfully integrated into conventional care of hospitalized cancer patients.

Secondary Aim:

The secondary aim is to evaluate the patient reported outcomes of their symptoms (pain, fatigue, anxiety) and feelings (happy, energetic, relaxed, and calm) before and after Reiki Therapy. The investigators' hypothesis is that there will be improvement of patients' symptoms/feelings score after the Reiki Therapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hospitalized hematology-oncology patients age 18 - 80
  • Able to speak English and complete surveys
  • Able to read, understand and sign inform consent.

排除标准

  • Patient unwilling for reiki therapy.
  • Unable to give written consent.
  • Already having received or receiving other reiki treatment.
  • Pregnant women. (As verbalized by participant)

结局指标

主要结局

Change in anxiety symptoms

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is not at all and 10 is unbearable

Change in pain pain symptoms

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is not at all and 10 is unbearable

Change in fatigue symptoms

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is not at all and 10 is unbearable

Change in feeling relaxed

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is best possible and 10 is worst possible

Change in feeling calm

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is best possible and 10 is worst possible

Change in feeling happy

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is best possible and 10 is worst possible

Change in feeling energized

时间窗: Baseline, approximately 2 hours

Measured using a numeric rating scale, where 0 is best possible and 10 is worst possible

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Brent A. Bauer

Principal Investigator

Mayo Clinic

研究点 (2)

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