Development of a Clinical Prediction Rulefor Neck Manipulation

NCT ID: NCT01620905

Last Updated: 2016-05-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

82 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-11-30

Study Completion Date

2011-06-30

Brief Summary

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Cervical spine manipulation has been shown to be helpful for some patients with neck pain. This study sought to determine factors which were predictive of which patients with neck pain would benefit from manipulation.

Detailed Description

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Conditions

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Mechanical Neck Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Cervical spine manipulation

Subjects received cervical spine manipulation

Group Type EXPERIMENTAL

Manipulation

Intervention Type PROCEDURE

Single level cervical spine joint manipulation

Interventions

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Manipulation

Single level cervical spine joint manipulation

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* age 18 to 60 years
* primary report of neck pain with or without unilateral upper extremity symptoms
* baseline neck disability index score of 10 points (out of 50) or greater

Exclusion Criteria

* any medical red flags suggesting that the etiology of symptoms might be nonmusculoskeletal
* diagnosis of cervical spinal stenosis (as identified in the patients' medical intake form)
* bilateral upper extremity symptoms
* evidence of central nervous system involvement
* history of whiplash injury within 6 weeks of the examination
* pending legal action regarding their neck pain
* 2 or more positive neurologic signs consistent with nerve root compression (changes in sensation, myotomal weakness, or decreased deep tendon reflexes)
* any history of cervical spine surgery, rheumatoid arthritis, osteoporosis, osteopenia, or ankylosing spondylitis.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Franklin Pierce University

OTHER

Sponsor Role collaborator

University of Colorado, Denver

OTHER

Sponsor Role collaborator

International Spine Pain Institute

OTHER

Sponsor Role collaborator

Universidad Rey Juan Carlos

OTHER

Sponsor Role collaborator

University of Nevada, Las Vegas

OTHER

Sponsor Role lead

Responsible Party

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Emilio J Puentedura, PT, DPT, PhD

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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UNLV PT Department

Las Vegas, Nevada, United States

Site Status

Countries

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United States

Other Identifiers

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UNLVPT08072806

Identifier Type: -

Identifier Source: org_study_id

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