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Hypoalgesic Effect of Cervical Manipulation

Not Applicable
Completed
Conditions
Pain
Interventions
Device: Global manipulation
Device: Especific manipulation
Registration Number
NCT03541538
Lead Sponsor
Universidade Federal de Sao Carlos
Brief Summary

This study evaluates the hypoalgesic effect of global and specific cervical joint manipulation in healthy individuals. At first the participants received one of the interventions and after 48 hours, the other.

Detailed Description

Cervical Joint Manipulation (CJM) are often used for pain treatment.

Joint manipulation generates a series of stimuli within the central nervous system through the activation of proprioceptors located in the joint capsule or muscles, stimulates the PAG, causing pain inhibition by activation of non-opioid descending inhibitory pathways.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
21
Inclusion Criteria
  • healthy subjects of both sexes
  • without pain complaints in the last 90 days
Exclusion Criteria
  • previous spinal surgeries
  • spinal canal stenosis
  • vertebral fracture
  • spondylolisthesis
  • cancer
  • acute infections
  • hemorrhagic disorders
  • active tuberculosis
  • deep vein thrombosis
  • osteoporosis
  • rheumatic diseases
  • metabolic diseases
  • cardiorespiratory diseases
  • smoking injury
  • musculoskeletal injury
  • use of pacemaker
  • women in menstrual period
  • pregnant women
  • use of pain-killers in the last 48 hours
  • use of anti-inflammatory drugs in the last 48 hours
  • previous joint manipulation treatments
  • aversion to cervical joint manipulation
  • positivity in the vertebral artery test
  • headache in the last seven days

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Global manipulationGlobal manipulationManual therapy performed in the cervical region in a non-specific way.
Especific manipulationEspecific manipulationmanual therapy performed specifically on the C6-7 segment
Primary Outcome Measures
NameTimeMethod
Pressure Pain Threshold at the posterior region of the forearm1 minute after the end of the intervention.

The subjects were placed supine on a stretcher with their elbows fully extended and the anterior portion of the forearm resting on the stretcher. Subjects were instructed to keep their eyes closed during attempts. The examiner used a Somedic Type II digital pressure algometer (Somedic Inc, Hörby, Sweden) on the posterior region of the forearm 10cm below the lateral epicondyle of the elbow towards the third finger, keeping the forearm in pronation. The pressure was then applied perpendicular to the skin at a rate of 40kPa / s using a 1cm2 flat circular probe covered with 1mm of rubber to prevent any skin pain caused by sharp metal edges.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ufscar - Universidade Federal de São Carlos

🇧🇷

São Carlos, São Paulo, Brazil

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