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Healing Touch and Relaxation Therapies in Cervical Cancer Patients - Article


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Clinical Trial: Healing Touch and Relaxation Therapies in Cervical Cancer Patients

This study is currently recruiting patients.

Sponsored by: National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)

Purpose

The purpose of this study is to evaluate the effects of healing touch and relaxation therapy on cervical cancer patients undergoing chemotherapy and radiation treatment.

Condition Treatment or Intervention Phase
Cervix Neoplasms
 Behavior: Healing Touch Therapy
 Behavior: Relaxation Therapy
Phase II

MedlinePlus related topics:  Cervical Cancer

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Official Title: Healing Touch in Advanced Cervical Cancer Patients: Immune Effects and Mechanisms

Further Study Details: 

Expected Total Enrollment:  70

Study start: September 2002;  Expected completion: May 2005

The side effects of chemotherapy and radiation treatment are often severe and can have devastating effects on the mental and physical well-being of cancer patients. This study will determine whether healing touch and relaxation therapy are effective in minimizing the side effects of chemotherapy and radiation treatment in cervical cancer patients.

Participants in this study will receive weekly chemotherapy and daily radiation treatments for 6 weeks. Participants will be randomly assigned to receive either standard care (SC), SC plus relaxation therapy, or SC plus healing touch therapy. The relaxation therapy consists of progressive muscle relaxation and guided imagery. The healing touch therapy involves an energy-based modality in which health care practitioners stimulate the energy fields surrounding the patient. A physician-completed assessment and measures of immune function will be used to assess the well-being and overall quality of life of participants.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Female

Criteria

Inclusion Criteria:

Exclusion Criteria:

  • Immunosuppressive disorders
  • Use of immunosuppressive medications
  • Transplant recipient
  • Metastatic or recurrent cervical cancer
  • History of any other type of cancer

Location and Contact Information


Iowa
      University of Iowa Hospital and Clinics, Iowa City,  Iowa,  52242,  United States; Recruiting
Heena H. Maiseri, BS  319-335-0145    heena-maiseri@uiowa.edu 
Susan K. Lutgendorf, PhD,  Principal Investigator

More Information

Study ID Numbers:  1 P20 AT-756-01
Record last reviewed:  September 2004
Last Updated:  October 13, 2004
Record first received:  June 7, 2004
ClinicalTrials.gov Identifier:  NCT00084123
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Resources



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Page Updated: September 6, 2005
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