跳至主要内容
临床试验/NCT00253708
NCT00253708已完成不适用

Body-Based Complementary Therapies for Patients With Cancer

Beth Israel Deaconess Medical Center2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2004年12月1日最近更新:
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
39
试验地点
2
主要终点
Anxiety

研究概览

简要总结

RATIONALE: Massage therapy may help relieve symptoms associated with cancer. It is not yet known which type of massage therapy is more effective in treating the symptoms of patients with cancer.

PURPOSE: This randomized clinical trial is studying different types of massage therapy to compare how well they work in treating the symptoms of patients with locally advanced or metastatic cancer.

详细描述

OBJECTIVES:

  • Compare the safety and tolerated dose (i.e., duration, techniques, and degree of pressure) of professional massage therapy vs professional simple presence (no touch) massage therapy vs usual care followed by caregiver massage therapy vs usual care in patients with locally advanced or metastatic cancer.
  • Correlate these therapies with pain, anxiety, depression, nausea, and shortness of breath in these patients.
  • Correlate these therapies with patient quality of life and caregiver anxiety and depression.
  • Determine the feasibility of teaching family caregivers how to provide massage therapy and the subsequent use of massage by the caregivers.
  • Determine the effects of caregiver massage therapy on patients and caregivers.
  • Determine the feasibility and acceptability among patients and massage therapists of a simple presence (no touch) massage therapy control group.

OUTLINE: This is a randomized, controlled, pilot study. Patients are randomized to 1 of 3 treatment arms.

  • Arm I (professional massage therapy): Hospitalized patients are offered massage therapy by a licensed massage therapist for 15-45 minutes once daily for the duration of their hospital stay. Outpatient oncology clinic patients are offered home-based massage therapy by a licensed massage therapist for 15-45 minutes once daily for 3 days.
  • Arm II (usual care): Patients receive usual care for symptom management.
  • Arm III (professional simple presence [no touch] massage therapy): Hospitalized patients are offered simple presence (no touch) massage therapy comprising a room visit by a licensed massage therapist who places his/her hands 12 inches over the patient without direct touch for 15-45 minutes. Treatment is offered once daily for the duration of the hospital stay. Outpatient oncology clinic patients are offered home-based simple presence (no touch) massage therapy by a licensed massage therapist for 15-45 minutes once daily for 3 days.

All patients are then randomized (a second time) to 1 of 2 treatment arms.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

massage

Experimental

Patients received 3 massage therapy visits from massage therapists in initial week with a duration of 15-45 minutes.NOTE: Intervention 'management of therapy complications' has not been included in any Arm/Group Descriptions.

Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: quality-of-life assessment (Procedure)

massage

Experimental

Patients received 3 massage therapy visits from massage therapists in initial week with a duration of 15-45 minutes.NOTE: Intervention 'management of therapy complications' has not been included in any Arm/Group Descriptions.

Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: management of therapy complications (Procedure)

massage

Experimental

Patients received 3 massage therapy visits from massage therapists in initial week with a duration of 15-45 minutes.NOTE: Intervention 'management of therapy complications' has not been included in any Arm/Group Descriptions.

Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: massage therapy (Procedure)

massage

Experimental

Patients received 3 massage therapy visits from massage therapists in initial week with a duration of 15-45 minutes.NOTE: Intervention 'management of therapy complications' has not been included in any Arm/Group Descriptions.

Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: pain therapy (Procedure)

massage

Experimental

Patients received 3 massage therapy visits from massage therapists in initial week with a duration of 15-45 minutes.NOTE: Intervention 'management of therapy complications' has not been included in any Arm/Group Descriptions.

Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: psychosocial assessment and care (Procedure)

no-touch control

Active Comparator

Patients received 3 no-touch therapy visits from massage therapists who provided no-touch without healing intention.Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: management of therapy complications (Procedure)

no-touch control

Active Comparator

Patients received 3 no-touch therapy visits from massage therapists who provided no-touch without healing intention.Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: massage therapy (Procedure)

no-touch control

Active Comparator

Patients received 3 no-touch therapy visits from massage therapists who provided no-touch without healing intention.Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: pain therapy (Procedure)

no-touch control

Active Comparator

Patients received 3 no-touch therapy visits from massage therapists who provided no-touch without healing intention.Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: psychosocial assessment and care (Procedure)

no-touch control

Active Comparator

Patients received 3 no-touch therapy visits from massage therapists who provided no-touch without healing intention.Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

干预措施: quality-of-life assessment (Procedure)

Usual care

No Intervention

Patients did not receive visits from massage therapists. Patients were intended to receive pain therapy, psychosocial assessment and care, and quality-of-life assessment

结局指标

主要结局

Anxiety

时间窗: From baseline to 1 week and from baseline to 1 month

0=no anxiety to 10=most severe anxiety

Alertness

时间窗: From baseline to 1 week and from baseline to 1 month

0=not at all alert to 10=most alert

Pain

时间窗: From baseline to 1 week and from baseline to one month

0=no pain to 10=most severe pain

次要结局

  • Quality of Life: Physical Well-being(From baseline to 1 week and from baseline to 1 month)
  • Quality of Life: Psychological Well-being(From baseline to 1 week and from baseline to 1 month)
  • Quality of Life: McGill Total(From baseline to 1 week and from baseline to 1 month)
  • Sleep(From baseline to 1 week and from baseline to 1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Russell Phillips

Principal Investigator

Beth Israel Deaconess Medical Center

研究点 (2)

Loading locations...

相似试验