We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Acupuncture for Anxiety in Women With Breast Cancer: A Feasibility Study

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00322504
First Posted: May 8, 2006
Last Update Posted: January 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of New Mexico
  Purpose

To assess the efficacy of acupuncture treatment in reducing symptoms of anxiety in women recently diagnosed with cancer.

• To assess the efficacy of acupuncture treatment on improving perceived quality of life in women recently diagnosed with cancer.


Condition Intervention
Breast Cancer Procedure: Accupuncture

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by University of New Mexico:

Estimated Enrollment: 10
Study Start Date: January 2006
Estimated Study Completion Date: September 2006
Detailed Description:
This is a feasibility study of acupuncture for anxiety reduction in women with breast cancer. Ten patients will be recruited at the UNM Cancer Research Treatment Center via the Breast Clinic and screened for anxiety. Treatment will consist of 10 acupuncture sessions over 5 weeks. Measures (Hopkins Symptom Checklist, Sheehan Disability Index) will be administered and analyzed for treatment effect on scores.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Woman age 18 years or older excluding the need for parental/guardian permission.
  • Histologic diagnosis of breast cancer.
  • Having a minimum anxiety score of 1.75 on the Hopkins Symptom Checklist (HSCL) with sufficient English language proficiency for the investigators to make this determination.
  • Able to give informed consent.
  • Willingness to participate in the study and receive 10 acupuncture treatments in 5 weeks.
  • Ability to fill out questionnaires and communicate with the research staff

Exclusion Criteria:

  • Males with breast cancer
  • Psychoses or a major personality disorder
  • Current use of opiates,
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00322504


Locations
United States, New Mexico
University of New Mexico
Albuquerque, New Mexico, United States, 87114
Sponsors and Collaborators
University of New Mexico
Investigators
Principal Investigator: Brian Shelley University of New Mexico
  More Information

ClinicalTrials.gov Identifier: NCT00322504     History of Changes
Other Study ID Numbers: INST 0520C
First Submitted: May 5, 2006
First Posted: May 8, 2006
Last Update Posted: January 7, 2010
Last Verified: November 2006

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases