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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01161758
Other study ID # PT0004
Secondary ID
Status Completed
Phase N/A
First received July 8, 2010
Last updated July 13, 2010
Start date April 2005
Est. completion date December 2005

Study information

Verified date November 2005
Source Curtin University of Technology
Contact n/a
Is FDA regulated No
Health authority Australia: Human Research Ethics Committee
Study type Interventional

Clinical Trial Summary

Passive accessory cervical mobilization is widely used as a clinical approach to the management of musculoskeletal pain of spinal origin. The purpose of the study is to determine if passive cervical mobilization can improve motor function in situations where motor performance is not impaired by the presence of pain.


Description:

Cervical mobilization has been shown to elicit effects on pain perception, autonomic function and motor function in subjects who experience musculoskeletal pain. The improvement in motor function may be a direct effect of the treatment or secondary to a hypoalgesic effect. This study aims to demonstrate whether it is possible to alter motor function following joint mobilization, in situations where motor performance is not impaired by pain.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 2005
Est. primary completion date October 2005
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- No history of neck or back pain over the last six months

- Without any previous experience with spinal manual therapy techniques

Exclusion Criteria:

- History of musculoskeletal or rheumatologic conditions

- Any kind of spinal surgery

- Dizziness

- Previous trauma to the cervical spine

- Neurological signs or symptoms

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Passive cervical mobilisation
Passive cervical mobilization which involved an oscillatory grade III unilateral postero-anterior mobilization applied to the left C5/C6 segment. The mobilization consisted of 3 periods of 1 minute applications with a resting period of 1 minute in between.
Manual contact
Manual contact control, which involved light manual contact on the left C5/C6 segment as if to perform the treatment technique. The light manual contact consisted of 3 periods of 1 minute applications with a resting period of 1 minute in between.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Curtin University of Technology

Outcome

Type Measure Description Time frame Safety issue
Primary Electromyography of sternocleidomastoid muscle. Measurement of sternocleidomastoid muscle activation during deep neck flexion. The degree of neck flexion is determined by a pressure biofeedback unit place underneath the neck. EMG of the left and right sternocleidomastoids are recorded for 5seconds at each level of neck flexion Pre intervention (baseline) and 1 minute post intervention No
Secondary Pressure pain threshold The algometer to measure pressure pain threshold was applied at a constant rate of 40 kPa/sec on the posterior aspect of the left and right articular pillar of C5/C6. Pre intervention (baseline) and 1 minute post intervention No
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