- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00779818
Electrical Acupuncture and Laser Therapy for Low Back Pain
October 23, 2008 updated by: Logan College of Chiropractic
This is a treatment for low back pain using electrical stimulation and laser for 6 weeks.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The purpose of the study is to investigate the effects of electroacupuncture and laser therapy to treat chronic low back pain.
Study Type
Interventional
Enrollment (Anticipated)
40
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
Chesterfield, Missouri, United States, 63006
- Recruiting
- Logan College of Chiropractic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Low back pain for over 6 weeks
Exclusion Criteria:
- Individuals with cancer
- Tuberculosis
- Pacemakers
- Pregnancy
- Osteoporosis
- Heart disease
- Kidney failure
- Thyroid disorders
- Diabetes
- Chronic disease
- Neurological diseases
- Skin or bleeding disorders
- Currently taking drugs or medications
- A health history questionnaire will be used to screen subjects
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
Treatment by electrical acupuncture
|
Treatment by electrical acupuncture
|
|
Experimental: Group 2
Treatment by laser
|
Treatment by laser
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Measure: Low Back Pain Disability Index, VAS Questionnaire, Revised Oswestry Pain Questionnaire
Time Frame: Before treatment and every two weeks for six weeks.
|
Before treatment and every two weeks for six weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2008
Primary Completion (Anticipated)
January 1, 2009
Study Completion (Anticipated)
January 1, 2009
Study Registration Dates
First Submitted
October 23, 2008
First Submitted That Met QC Criteria
October 23, 2008
First Posted (Estimate)
October 24, 2008
Study Record Updates
Last Update Posted (Estimate)
October 24, 2008
Last Update Submitted That Met QC Criteria
October 23, 2008
Last Verified
October 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RD1117060051
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.