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CompletedNCT00401063Updated May 30, 2013

Usefulness of Acupuncture in Cancer Pain and Quality of Life

An interventional study of Acupuncture in Cancer and Pain, sponsored by Southern California University of Health Sciences. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-05-30.

Sponsored by Southern California University of Health Sciences · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
11
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Cancer
  • Pain

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Keywords

  • Cancer
  • Acupuncture
  • Cancer Pain
  • Quality of life
03

In context

Cancer Pain

338 studies on the registry are indexed under Cancer Pain; 71 are open to participants now.

This study's enrollment of 11 is below the median of 60 across 254 interventional studies indexed under Cancer Pain.

Browse Cancer Pain studies →

Lead sponsor

Southern California University of Health Sciences is the lead sponsor of 11 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
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

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
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
11 participants (actual)

Study arms

  • Other
    Single arm

    Acupuncture treatment

    Device: Acupuncture

Interventions

  • DeviceAcupuncture

    Acupuncture treatment twice a day for eight weeks

06

What researchers measure

Primary outcomes

  1. EORTC QLQ-30 Quality of Life Questionnaire for Cancer Patients

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

  2. Visual Analogue Scale

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

Secondary outcomes

  1. BDI Psychological Assessment

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

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Study locations

2 sites
  • University Health Center
    Pasadena, California 91104, United States
  • Southern California University of Health Sciences
    Whittier, California 90604, United States
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00401063
Lead sponsor
Southern California University of Health Sciences
Responsible party
Sivarama Vinjamury (Professor, Southern California University of Health Sciences) — Principal investigator
First posted
Nov 17, 2006
Start date
Sep 2006
Primary completion
Aug 2007
Completion
Oct 2007
Last update
May 30, 2013

Study contacts

Sivarama P Vinjamury, MD, MAOM
principal investigator · Southern California University of Health Sciences

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2013. You cannot join it, but the record below documents what was studied.

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