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临床试验/NCT01553578
NCT01553578已完成不适用

The Efficacy of Healing Touch Versus Guided Imagery on Pain, Fatigue, Nausea, and Anxiety in Patients' Receiving Outpatient Chemotherapy

Wake Forest University Health Sciences2 个研究点 分布在 1 个国家目标入组 244 人开始时间: 2012年2月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
244
试验地点
2
主要终点
Change scores for each patient on fatigue scale

研究概览

简要总结

This randomized clinical trial studies healing touch or guided imagery in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy. Healing touch and guided imagery may help treat complications caused by chemotherapy. It is not yet known whether healing touch or guided imagery is more effective in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy

详细描述

PRIMARY OBJECTIVES:

I. To determine if the provision of healing touch or guided imagery during outpatient chemotherapy is associated with decreased pain, fatigue, nausea and anxiety when compared to standard outpatient treatment protocols.

OUTLINE: Patients are randomized to 1 of 3 treatment arms.

ARM A: Patients receive 30 minutes of healing touch therapy comprising magnetic clearing, pain drains, hands in motion/hands still and mind clearing.

ARM B: Patients listen to guided imagery audiotapes for 30 minutes

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

入选标准

  • Adult patients at the outpatient chemotherapy area will be enrolled without consideration for type of cancer or chemotherapeutic agents to be used

排除标准

  • 未提供

研究组 & 干预措施

Arm A (healing touch therapy)

Experimental

Patients receive 30 minutes of healing touch therapy consisting of magnetic clearing, pain drains, hands in motion/hands still and mind clearing.

干预措施: questionnaire administration (Other)

Arm A (healing touch therapy)

Experimental

Patients receive 30 minutes of healing touch therapy consisting of magnetic clearing, pain drains, hands in motion/hands still and mind clearing.

干预措施: therapeutic touch (Procedure)

Arm A (healing touch therapy)

Experimental

Patients receive 30 minutes of healing touch therapy consisting of magnetic clearing, pain drains, hands in motion/hands still and mind clearing.

干预措施: management of therapy complications (Behavioral)

Arm B (guided imagery)

Experimental

Patients listen to guided imagery audiotapes for 30 minutes.

干预措施: questionnaire administration (Other)

Arm B (guided imagery)

Experimental

Patients listen to guided imagery audiotapes for 30 minutes.

干预措施: management of therapy complications (Behavioral)

Arm C (standard care)

Active Comparator

Patients receive standard of care.

干预措施: questionnaire administration (Other)

Arm C (standard care)

Active Comparator

Patients receive standard of care.

干预措施: standard follow-up care (Procedure)

结局指标

主要结局

Change scores for each patient on fatigue scale

时间窗: Approximately 6 months

Collected using a 10 point visual analog scale for pain, fatigue, nausea, and anxiety. Analyzed initially using descriptive statistics. Compared among the 3 groups using one-way analysis of variance (ANOVA) models and 2-sample t-tests.

Change scores for each patient on anxiety scale

时间窗: Approximately 6 months

Collected using a 10 point visual analog scale for pain, fatigue, nausea, and anxiety. Analyzed initially using descriptive statistics. Compared among the 3 groups using one-way analysis of variance (ANOVA) models and 2-sample t-tests.

Change scores for each patient on pain scale

时间窗: Approximately 6 months

Collected using a 10 point visual analog scale for pain, fatigue, nausea, and anxiety. Analyzed initially using descriptive statistics. Compared among the 3 groups using one-way analysis of variance (ANOVA) models and 2-sample t-tests.

Change scores for each patient on nausea scale

时间窗: Approximately 6 months

Collected using a 10 point visual analog scale for pain, fatigue, nausea, and anxiety. Analyzed initially using descriptive statistics. Compared among the 3 groups using one-way analysis of variance (ANOVA) models and 2-sample t-tests.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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