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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01168986
Other study ID # 340-2009
Secondary ID 340-2009
Status Recruiting
Phase Phase 1/Phase 2
First received July 22, 2010
Last updated March 17, 2015
Start date September 2009
Est. completion date August 2015

Study information

Verified date March 2015
Source University of Florida
Contact Joel E Bialosky, PhD
Phone 352-273-8636
Email bialosky@phhp.ufl.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study is comparing the effectiveness of a mechanical manual therapy device to a specific exercise to no treatment in individuals experiencing neck pain. We are interested in the effects of the interventions on neck pain, disability related to neck pain, and pain sensitivity.


Recruitment information / eligibility

Status Recruiting
Enrollment 66
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- currently experiencing neck pain which does not extend below the elbow

- pain at least 4/10 over the past 24 hours

- appropriate for conservative management of neck pain

- english speaking

Exclusion Criteria:

- surgery to the neck within the past 6 months

- systemic problem know to affect sensation

- other chronic pain condition other than neck pain

- neck pain as the result of trauma such as whiplash

- neck pain as the result of a fracture

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Pulstar Multiple Impulse Therapy
Use of the PulStar Multiple Impulse Therapy (Sense Technology). A mechanical manual therapy device.
Exercise
Participants perform an exercise to strengthen the deep neck flexors

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain score on a numeric rating scale a 101 point numeric rating scale of neck pain with 0 indicating no pain at all and 100 indicating the worst pain imaginable 2 weeks No
Primary disability on the neck disability index A functional questionnaire (the neck disability index) to assess self report of disability related to neck pain 2 weeks No
Primary pain sensitivity using a numeric rating scale and a visual analog scale self report of pain in corresponding to standardized pressure and thermal stimuli 2 week No
Secondary range of motion neck range of motion including flexion, extension, sidebending, and rotation 2 weeks No
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