Proposal to Evaluate the Efficacy of the InterX 5000 in the Treatment of Chronic Neck and Shoulder Pain
NCT00587626 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2010-06-25
Summary
The purpose of the proposed study is to evaluate the efficacy of the InterX 5000 in relieving chronic neck and shoulder pain. This study will focus on the efficacy of treating patients who have functional limitations in activity because of chronic/recurrent neck or shoulder pain.
H1: InterX therapy will have a moderate effect to reduce pain.
H2: Functional gains will be greater in patients receiving InterX therapy compared to those who received placebo treatment.
H3: Chronic neck and shoulder pain is more prevalent in patients who exhibit radiographic evidence of degenerative spondylosis/arthrosis of the cervical spine.
Conditions
- Neck Pain
- Shoulder Pain
- Cervical Pain
Interventions
- DEVICE
-
Inactive InterX 5000
Patients will receive will receive InterX placebo treatment 3 times a week for 4 weeks.
- DEVICE
-
InterX 5000 Treatment
Patients will receive will receive InterX treatment 3 times a week for 4 weeks.
Sponsors & Collaborators
-
Canadian Memorial Chiropractic College
collaborator OTHER -
Neuro Resource Group
collaborator INDUSTRY -
Hamilton Health Sciences Corporation
lead OTHER
Principal Investigators
-
Linda J Woodhouse, PhD · McMaster University
-
John J Triano, DC, PhD · Canadian Memorial Chiropractic College
-
Vickie Galea, PhD · McMaster University
-
H Stephen Injeyan, PhD, DC · Canadian Memorial Chiropractic College
-
Joy MacDermid, PhD · McMaster University
-
Marion McGregor, DC, PhD · Canadian Memorial Chiropractic College
-
Michael Pierrynowski, PhD · McMaster University
-
Richard Ruegg, PhD, DC · Canadian Memorial Chiropractic College
-
Julita A Teodorczyk-Injeyan, PhD · Canadian Memorial Chiropractic College
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 66 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-08-31
- Primary Completion
- 2009-08-31
- Completion
- 2009-12-31
Countries
- Canada
Study Locations
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