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Home > "A" Clinical Trials Conditions > Acupuncture to Improve Quality of Life in Patients With Advanced Cancer  Acupuncture to Improve Quality of Life in Patients With Advanced Cancer
Acupuncture to Improve Quality of Life in Patients With Advanced Cancer
For Condition: Ovarian Cancer
Status: Recruiting
Sponsor(s): National Center for Complementary and Alternative Medicine (NCCAM) , National Cancer Institute (NCI)
Synopsis: This study will test the effectiveness of acupuncture as a complementary therapy for advanced cancer by comparing symptoms and quality of life before and after 8 weeks of acupuncture treatments.
Details: A large percentage of the practice and use of complementary and alternative medicine (CAM) in the United States is focused on cancer. Whether the CAM use is aimed at reducing one's risk of developing cancer or improving the quality of life of a cancer patient during treatment or at the end of life, the public focus on CAM and cancer has created a driving force for cancer centers to address the efficacy and science of these methods. Currently, the majority of cancer patients do not receive adequate palliative care. Acupuncture has been shown to be effective in the treatment of pain and nausea and has also been shown to improve one's general well-being. Acupuncture also has some effectiveness in relieving symptoms of anxiety and depression. This study will evaluate the efficacy of acupuncture by Traditional Chinese Medicine clinicians to address the quality of life and symptoms of patients with incurable cancer. Women with recurrent metastatic ovarian cancer and similar patients with advanced cancer who are ambulatory and receiving conventional palliative care will be enrolled in this study. Patients will continue to receive high-quality, conventional clinical interventions, including chemotherapy and pain and symptom reduction programs. Patients will also receive 8 weeks of acupuncture. Evaluation tools such as Satisfaction with Life Domains Scale for Cancer (SLDS-C), Brief Pain Inventory, and Rotterdam Symptom Check List will be used to assess the acupuncture intervention.
Eligibility:
Study Type: Interventional, Treatment, Non-Randomized, Open Label, Single Group Assignment, Efficacy Study
Minimum Age/Maximum Age: 21 Years/
Genders: Female
Protocol Entry Criteria: Inclusion Criteria - Advanced cancer patients, primarily ovarian cancer patients - Undergoing palliative care treatment - Ambulatory - Symptomatic with pain, nausea, and/or an inadequate quality of life - Platelets > 25,000/mm3 - ANC > 500 cells/mm3 Exclusion Criteria - Acupuncture treatment during the 6 months prior to study entry - History of bleeding disorder, such as hemophilia or von Willebrand disease - Acute psychosis
Total Enrollment: 40
Location and Contact Information:
Overall Study Official:
DavidRosenthal, Principal Investigator, Dana-Farber/Harvard Cancer Center
Dana-Farber Cancer Institute *Recruiting*
Boston, Massachusetts, 02115
United States
Recruiting David Rosenthal 617-495-2010
Additional Information:
Study ID Numbers: 1 R21 AT01010-01;
Study Start Date: September 2001
Record last reviewed: October 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00070967
Other Ovarian Cancer Studies:
1. A study of the safety and effects of EMD 72000 in subjects with recurrent ovarian cancer
2. Gemzar (gemcitabine) and Alimta (pemetrexed) in the Treatment of Patients with Recurrent Platinum-Sensitive and Platinum-Resistant Ovarian or Peritoneal Cancer
3. Acupuncture to Improve Quality of Life in Patients With Advanced Cancer
4. Clinical Trial for Ovarian Cancer (OvaRex®)
5. Breast Imaging Studies in Women at High Genetic Risk of Breast Cancer: Menstrual Cycle Study
Related Studies:
Other Ovarian Cancer Clinical Trials
Other Massachusetts Clinical Trials
Other Boston Clinical Trials
Acupuncture to Improve Quality of Life in Patients With Advanced Cancer
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