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Clinical Trials/NCT02826590
NCT02826590
Completed
Not Applicable

The Effects of Spinal Mobilizations on Symptoms, Neck 3D Movement, Neck Muscle Electromyography and Sympathetic Nervous System Activity in People With Neck Pain

King's College London1 site in 1 country40 target enrollmentJune 2016
ConditionsNeck Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck Pain
Sponsor
King's College London
Enrollment
40
Locations
1
Primary Endpoint
Change in muscle activity assessed by neck muscle electromyography
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study investigates the effects of spinal mobilizations on symptoms, 3D movement of the neck, neck muscle electromyography and sympathetic nervous system activity in people with neck pain.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
July 31, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Intermittent neck pain
  • That worsens or improves with certain neck movements or positions
  • Has not been caused by a blow, fall or accident

Exclusion Criteria

  • Cervicobrachialgia
  • Has been treated with or is awaiting neck surgery
  • Diagnosed with a particular inflammatory disease or spinal condition
  • Where treatment with cervical mobilizations is contraindicated

Outcomes

Primary Outcomes

Change in muscle activity assessed by neck muscle electromyography

Time Frame: Baseline and 2 minutes after intervention

Change in 3D neck movement assessed with a 10 camera Vicon system

Time Frame: Baseline and 2 minutes after intervention

Change in sympathetic nervous system activity assessed by measuring right hand finger temperature

Time Frame: Baseline for 2 minutes immediately before intervention, during intervention (15 minutes) and for 2 minutes immediately after intervention

Measurement unit: degrees celsius

Change in sympathetic nervous system activity assessed by measuring right hand finger galvanic response

Time Frame: Baseline for 2 minutes immediately before intervention, during intervention (15 minutes) and for 2 minutes immediately after intervention

Measurement unit: microsiemens

Global rating of change scale

Time Frame: Baseline and 10 minutes after intervention

Study Sites (1)

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