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Clinical Trials/NCT04001218
NCT04001218
Completed
N/A

Neck Pain - Motor and Sensory Aspects

Aalborg University1 site in 1 country28 target enrollmentApril 9, 2015

Overview

Phase
N/A
Intervention
Injection of hypertonic saline
Conditions
Healthy
Sponsor
Aalborg University
Enrollment
28
Locations
1
Primary Endpoint
Change in head repositioning accuracy
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study investigates if/how an experimentally applied neck muscle pain influences head repositioning error in healthy participants.

Detailed Description

Healthy volunteers will participate in a single session study with a crossover design. During the study healthy participants will be randomized to either receive a injection of hypertonic saline (painful injection) or isotonic saline (control injection) in a neck muscle. Head repositioning accuracy will be assessed with and without performing a cognitive task.

Registry
clinicaltrials.gov
Start Date
April 9, 2015
End Date
September 22, 2015
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Aalborg University
Responsible Party
Principal Investigator
Principal Investigator

Steffan Wittrup Christensen

Associate professor

Aalborg University

Eligibility Criteria

Inclusion Criteria

  • Healthy men and women aged 18-50 years
  • Right handed
  • Able to speak, read and understand Danish or English
  • Normal pain free neck and shoulder range of motion

Exclusion Criteria

  • Pain from the neck or shoulder area
  • Prior surgery in neck or shoulder
  • Pregnancy
  • Drug addiction defined as the use of cannabis, opioids or other drugs
  • Self reported neurologic, musculoskeletal or mental illnesses

Arms & Interventions

Painful condition

Participants will be injected with 0.5ml hypertonic saline (5.8%) into a neck muscle

Intervention: Injection of hypertonic saline

Control condition

Participants will be injected with 0.5ml Isotonic saline (0.9%) into a neck muscle

Intervention: Injection of Isotonic saline

Outcomes

Primary Outcomes

Change in head repositioning accuracy

Time Frame: Within session (session lasts approximately 2 hours)

Participants will be blindfolded and asked asked to, from a neutral position, to move the head into full range of motion before returning to to a neutral position again. The difference between the start and end position will be used as an estimate of head repositioning error.

Secondary Outcomes

  • Change in perceived pain(Within session (session lasts approximately 2 hours))
  • Change in perceived performance of head repositioning accuracy test(Within session (session lasts approximately 2 hours))

Study Sites (1)

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