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Clinical Trials/NCT01553578
NCT01553578
Completed
N/A

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

Wake Forest University Health Sciences1 site in 1 country244 target enrollmentFebruary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anxiety Disorder
Sponsor
Wake Forest University Health Sciences
Enrollment
244
Locations
1
Primary Endpoint
Change scores for each patient on fatigue scale
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

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

Detailed Description

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 ARM C: Patients receive standard of care.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
February 2013
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change scores for each patient on fatigue scale

Time Frame: 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

Time Frame: 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

Time Frame: 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

Time Frame: 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.

Study Sites (1)

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