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Clinical Trials/NCT03493334
NCT03493334
Completed
Not Applicable

Impacto do Feedback Visual da região Posterior da Coluna Cervical, na Intensidade da Dor e Amplitude de Movimento, em Utentes Com Dor Cervical crónica idiopática

Aveiro University1 site in 1 country42 target enrollmentApril 15, 2018
ConditionsNeck Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck Pain
Sponsor
Aveiro University
Enrollment
42
Locations
1
Primary Endpoint
Neck pain intensity
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The objective of this study is to evaluate the impact of visual feedback of the posterior region of the cervical spine on pain intensity and range of motion.

Detailed Description

60 patients with chronic idiopathic neck pain will be randomly assigned into one of two groups: a group receiving visual feedback when performing 10 repetitions of each of neck movements (flexion, extension, side-flexion and rotation) and a group performing the same task without visual feedback. Participants will be assessed for pain intensity, pain location, disability, range of motion, kinesiophobia, catastrophizing and anxiety both at baseline and after visual the intervention (i.e., neck movements with and without visual feedback).

Registry
clinicaltrials.gov
Start Date
April 15, 2018
End Date
June 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Aveiro University
Responsible Party
Principal Investigator
Principal Investigator

Anabela G Silva

Assistant Professor

Aveiro University

Eligibility Criteria

Inclusion Criteria

  • To have idiopathic neck pain defined as neck pain unrelated to any known pathology or lesion felt at least once a week in the last 3 months, located between the nuchal line and a horizontal line passing through T1 and pain intensity of at least 3 in the visual analogue scale.

Exclusion Criteria

  • History of cervical or facial trauma, radiculopathy, history of surgery in the vertebral segment in question, congenital anomalies involving the spine (cervical, thoracic and lumbar spine) or any neurological or rheumatic pathology, and, finally, evidence of significant visual changes, or of deficits not corrected by lenses or glasses.

Outcomes

Primary Outcomes

Neck pain intensity

Time Frame: Immediately after the intervention (at 30 minutes)

Measured using a 10 cm visual analogue scale

Secondary Outcomes

  • Kinesiophobia(Immediately after the intervention (at 30 minutes))
  • Time for pain to return to baseline levels(Immediately after the intervention (at 30 minutes))
  • Pain location(Immediately after the intervention (at 30 minutes))
  • Neck range of motion(Immediately after the intervention (at 30 minutes))
  • Neck perception(Immediately after the intervention (at 30 minutes))
  • Anxiety(Immediately after the intervention (at 30 minutes))
  • Pain disability(Immediately after the intervention (at 30 minutes))
  • Catastrophyzing(Immediately after the intervention (at 30 minutes))

Study Sites (1)

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