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N/A N=28 Randomized Single-blind Basic Science

The Effect of Manipulation of the Cervical Spine on Pain Biomarkers

Neck Pain, Posterior

Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Aug 2019
Primary outcome: Primary: Plasma Concentration of Oxytocin — 154.5; 158.8 ug/ml

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
HVLAT manipulation (Procedure); Sham HVLAT manipulation (Procedure)
Age
Adult · 20+ yrs
Sex
Female
Sponsor
Loma Linda University
Primary completion
Sep 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Plasma Concentration of Oxytocin
185.1; 189.1
PRIMARY
Plasma Concentration of Oxytocin
185.1; 189.1
SECONDARY
Plasma Concentration of Neurotensin
136.4; 131.6
SECONDARY
Plasma Concentration of Neurotensin
136.4; 131.6
SECONDARY
Plasma Concentration of Orexin A
73.8; 67.3
SECONDARY
Plasma Concentration of Orexin A
73.8; 67.3
SECONDARY
Plasma Concentration of Cortisol
108.1; 139.7
SECONDARY
Plasma Concentration of Cortisol
108.1; 139.7

Summary

This study evaluates the effect of high-velocity low-amplitude thrust (HVLAT) manipulation to the cervical spine on neuropeptide expression as determined by the plasma concentration of oxytocin, neurotensin, orexin A and cortisol; and Examine the effect of HVLAT manipulation on pain perception in symptomatic females with non-specific mechanical cervical spine pain

Eligibility Criteria

Inclusion Criteria

  • 20 - 45 years of age
  • A score of 10 or more out of 50 on the Neck Disability Index (NDI) questionnaire
  • Symptoms of pain present for 30 days or less and no pain symptoms below your shoulder

Exclusion Criteria

  • Serious condition (such as cancer, spondylolisthesis, rheumatoid arthritis, or ankylosing spondylitis)
  • Cervical spinal stenosis signs (such as incoordination in hands, arms and legs, inability of walking at a brisk pace, or bowel and bladder incontinence)
  • Nerve root compression (such as changes in sensation, muscle weakness, or decreased reflexes)
  • Works the night shift
  • Steroid medication within 3 months
  • Pregnancy or postpartum
  • Pending legal action regarding their neck pain
  • History of whiplash associated disorder and/or cervical spine surgery
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03176654). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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