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Healing Touch in Treating Fatigue in Women Undergoing Radiation Therapy for Breast Cancer

Primary Purpose

Breast Cancer, Depression, Fatigue

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bio-field energy therapy
fatigue assessment and management
psychosocial assessment and care
quality-of-life assessment
therapeutic touch
Sponsored by
Vanderbilt-Ingram Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring fatigue, depression, psychosocial effects of cancer and its treatment, stage I breast cancer, stage II breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, stage IIIC breast cancer, recurrent breast cancer

Eligibility Criteria

21 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven breast cancer
  • Receiving post lumpectomy or post mastectomy radiation therapy (RT)
  • Eastern Cooperative Oncology Group performance status of 0, 1 or 2
  • Prescribed a minimum of 5 weeks of RT
  • Between the ages of 21 and 75
  • Able to speak English.
  • Provides written informed consent

Exclusion Criteria:

  • Documented active psychiatric illness
  • Documented cognitive impairment that would preclude the ability to provide informed consent.
  • Stage IV breast cancer
  • Receiving concurrent chemotherapy and RT

Sites / Locations

  • Vanderbilt-Ingram Cancer Center - Cool Springs
  • Vanderbilt-Ingram Cancer Center at Franklin
  • Vanderbilt-Ingram Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Radiotherapy/Supportive Care (A)

Control ARM (B)

Arm Description

Patients receive radiotherapy and healing touch therapy from a healing touch therapist once a week for the duration of their radiotherapy

Patients receive radiotherapy and sham healing touch therapy from a sham healing touch therapist once a week for the duration of their therapy

Outcomes

Primary Outcome Measures

Fatigue Using the Brief Fatigue Inventory (BFI)
9-items with an 11-point rating scale measures intensity of fatigue (3 items, 0 = no fatigue to 10 = fatigue as bad as you can imagine) and interference of fatigue on daily life (6 items, 0 = does not interfere to 10 = completely interferes. Each participant's score is summed with a possible minimum score of 0 and a possible maximum score of 90. A mean score was then determined.

Secondary Outcome Measures

Quality of Life as Measured by the Functional Assessment of Cancer Therapy-Breast Form (FACT-B)
36 items that measure general quality of life (27 items) and specific breast cancer concerns (9 items) on a 5-point rating scale with 0 = not at all to 4 = very much. Minimum (worst quality of life) possible score = 0 and maximum (best quality of life) possible score = 144. Physical and emotional well-being scores were reverse coded and sub scale scores were summed. Median scores for baseline and at 6 weeks were determined
Intensity of Anxiety and Depression
Measured on the Hospital Anxiety and Depression Scale, 14 items on a 4-point scale scored from 0 = not at all (best feeling) to 3 = very often (worst feeling). Scores are summed and range from a minimum of 0 (no anxiety or depression) to 42 (worst anxiety or depression)and a median for each arm is determined at the specified timepoints.

Full Information

First Posted
December 14, 2007
Last Updated
August 4, 2012
Sponsor
Vanderbilt-Ingram Cancer Center
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00574145
Brief Title
Healing Touch in Treating Fatigue in Women Undergoing Radiation Therapy for Breast Cancer
Official Title
Examining the Effect of Healing Touch on Radiotherapy-induced Fatigue
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt-Ingram Cancer Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Healing touch therapy may be effective in lessening fatigue in women with breast cancer who are undergoing radiation therapy. PURPOSE: This randomized clinical trial is studying how well healing touch works in treating fatigue in women undergoing radiation therapy for breast cancer.
Detailed Description
OBJECTIVES: To determine the ability to recruit and retain patients with breast cancer receiving curative radiotherapy in a Complementary and Alternative Medicine trial. To determine the acceptability of weekly healing touch therapy to patients with breast cancer who receive curative radiotherapy. To examine the effect of healing touch on fatigue and quality of life for patients with breast cancer receiving radiotherapy as a component of therapy. OUTLINE: Patients are stratified by type of treatment (radiotherapy alone vs chemotherapy completed prior to radiotherapy) Arm I:Patients receive healing-touch therapy administered once a week for 45 minutes by a healing-touch therapist for the duration of radiotherapy. Arm II: Patients receive sham-therapy administered once a week for 45 minutes by a sham-practitioner (NOT a healing-touch therapist) for the duration of radiotherapy. Patients complete the Hospital Anxiety and Depression Scale (HAD) and a demographic variables form (age, race/ethnicity, marital status, employment) at baseline. Patient fatigue is measured on a weekly basis throughout radiotherapy with completion of the Brief Fatigue Inventory (BFI). The Functional Assessment of Cancer Therapy-Breast form (FACT-B) is completed at baseline and the end of radiotherapy. Patients undergo a 20-minute interview at the end of study to determine the acceptability of the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Depression, Fatigue
Keywords
fatigue, depression, psychosocial effects of cancer and its treatment, stage I breast cancer, stage II breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, stage IIIC breast cancer, recurrent breast cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Radiotherapy/Supportive Care (A)
Arm Type
Experimental
Arm Description
Patients receive radiotherapy and healing touch therapy from a healing touch therapist once a week for the duration of their radiotherapy
Arm Title
Control ARM (B)
Arm Type
Sham Comparator
Arm Description
Patients receive radiotherapy and sham healing touch therapy from a sham healing touch therapist once a week for the duration of their therapy
Intervention Type
Procedure
Intervention Name(s)
Bio-field energy therapy
Other Intervention Name(s)
biofield therapy
Intervention Description
Practitioner's hands to influence the human energy field surrounding the patient's body.
Intervention Type
Procedure
Intervention Name(s)
fatigue assessment and management
Intervention Description
duration
Intervention Type
Procedure
Intervention Name(s)
psychosocial assessment and care
Intervention Description
duration
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Intervention Description
duration
Intervention Type
Procedure
Intervention Name(s)
therapeutic touch
Intervention Description
Practitioner's hands to influence the human energy field surrounding the patient's body
Primary Outcome Measure Information:
Title
Fatigue Using the Brief Fatigue Inventory (BFI)
Description
9-items with an 11-point rating scale measures intensity of fatigue (3 items, 0 = no fatigue to 10 = fatigue as bad as you can imagine) and interference of fatigue on daily life (6 items, 0 = does not interfere to 10 = completely interferes. Each participant's score is summed with a possible minimum score of 0 and a possible maximum score of 90. A mean score was then determined.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Quality of Life as Measured by the Functional Assessment of Cancer Therapy-Breast Form (FACT-B)
Description
36 items that measure general quality of life (27 items) and specific breast cancer concerns (9 items) on a 5-point rating scale with 0 = not at all to 4 = very much. Minimum (worst quality of life) possible score = 0 and maximum (best quality of life) possible score = 144. Physical and emotional well-being scores were reverse coded and sub scale scores were summed. Median scores for baseline and at 6 weeks were determined
Time Frame
baseline and 6 weeks
Title
Intensity of Anxiety and Depression
Description
Measured on the Hospital Anxiety and Depression Scale, 14 items on a 4-point scale scored from 0 = not at all (best feeling) to 3 = very often (worst feeling). Scores are summed and range from a minimum of 0 (no anxiety or depression) to 42 (worst anxiety or depression)and a median for each arm is determined at the specified timepoints.
Time Frame
baseline and off-radiation at 5 to 7 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven breast cancer Receiving post lumpectomy or post mastectomy radiation therapy (RT) Eastern Cooperative Oncology Group performance status of 0, 1 or 2 Prescribed a minimum of 5 weeks of RT Between the ages of 21 and 75 Able to speak English. Provides written informed consent Exclusion Criteria: Documented active psychiatric illness Documented cognitive impairment that would preclude the ability to provide informed consent. Stage IV breast cancer Receiving concurrent chemotherapy and RT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy Wells, DNSc, RN
Organizational Affiliation
Vanderbilt-Ingram Cancer Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fern Fitzhenry, PhD, RN
Organizational Affiliation
Vanderbilt-Ingram Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt-Ingram Cancer Center - Cool Springs
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37064
Country
United States
Facility Name
Vanderbilt-Ingram Cancer Center at Franklin
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37064
Country
United States
Facility Name
Vanderbilt-Ingram Cancer Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232-6838
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24105358
Citation
FitzHenry F, Wells N, Slater V, Dietrich MS, Wisawatapnimit P, Chakravarthy AB. A randomized placebo-controlled pilot study of the impact of healing touch on fatigue in breast cancer patients undergoing radiation therapy. Integr Cancer Ther. 2014 Mar;13(2):105-13. doi: 10.1177/1534735413503545. Epub 2013 Oct 7.
Results Reference
derived

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Healing Touch in Treating Fatigue in Women Undergoing Radiation Therapy for Breast Cancer

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