Skip to main content
Clinical Trials/NCT00401063
NCT00401063CompletedNot Applicable

Acupuncture Case Series: Cancer Pain and Quality of Life

Southern California University of Health Sciences2 sites in 1 country11 target enrollmentStarted: September 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
11
Locations
2
Primary Endpoint
EORTC QLQ-30 Quality of Life Questionnaire for Cancer Patients

Study Overview

Brief Summary

The purpose of this study is to assess the effects of acupuncture on aspects of health including pain, energy level, sleep quality, activities of daily living and appetite.

Detailed Description

After receiving permission from the attending physician each study participant who meets the inclusion criteria will then undergo a physical examination and fill out several questionnaires. Each participant will undergo one to three treatments per week for a period of eight weeks. There will be one follow-up visit on the twelfth week. Participation in this study is free of charge, including all exams, treatment and informational material.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Confirmed diagnosis of cancer by an MD/oncologist
  • •Age of 18 or older
  • •Baseline pain score of 3 or above on 0-10 rating scale
  • •In the evaluation of the treating physician or medically-qualified investigator, the patient's pain syndrome is the result of underlying cancer or cancer treatment
  • •Being ambulatory
  • •Permission from the treating physician (MD/oncologist)
  • •Platelet count of 50,000 or greater

Exclusion Criteria

  • •Acupuncture treatment in past four weeks
  • •Neutropenia defined as ANC (absolute neutrophil count) < 1000/ml
  • •Inability to obtain permission from the treating physician
  • •Unwillingness to sign informed consent form
  • •Involvement in litigation
  • •Simultaneous infection with HIV or Hepatitis C virus
  • •Unable to present for follow up

Arms & Interventions

Single arm

Other

Acupuncture treatment

Intervention: Acupuncture (Device)

Outcomes

Primary Outcomes

EORTC QLQ-30 Quality of Life Questionnaire for Cancer Patients

Time Frame: Every two weeks, 0, 2, 4, 6, 8 and 12

Visual Analogue Scale

Time Frame: Every two weeks, 0,2,4,6,8, and 12 weeks

Secondary Outcomes

  • BDI Psychological Assessment(Every two weeks, 0, 2, 4, 6, 8 and 12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sivarama Vinjamury

Professor

Southern California University of Health Sciences

Study Sites (2)

Loading locations...

Similar Trials