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Visual Feedback in Chronic Neck Pain

Not Applicable
Completed
Conditions
Neck Pain
Interventions
Other: Visual feedback
Other: No visual feedback
Registration Number
NCT03493334
Lead Sponsor
Aveiro University
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).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
42
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Visual feedbackVisual feedbackParticipants in this group will receive visual feedback of their neck when performing 10 repetitions of each of neck movements (flexion, extension, side-flexion and rotation).
No visual feedbackNo visual feedbackParticipants in this group will perform 10 repetitions of each of neck movements (flexion, extension, side-flexion and rotation) without feedback.
Primary Outcome Measures
NameTimeMethod
Neck pain intensityImmediately after the intervention (at 30 minutes)

Measured using a 10 cm visual analogue scale

Secondary Outcome Measures
NameTimeMethod
KinesiophobiaImmediately after the intervention (at 30 minutes)

Measured using the Tampa Scale of Kinsesiophobia (Range: 13-52 and higher values are indicative of a higher fear of movement.

Time for pain to return to baseline levelsImmediately after the intervention (at 30 minutes)

Measured with a chronometer

Pain locationImmediately after the intervention (at 30 minutes)

Measured using a body chart

Neck range of motionImmediately after the intervention (at 30 minutes)

Measured using a goniometer

Neck perceptionImmediately after the intervention (at 30 minutes)

Assessed by asking participants to draw their neck as they perceive it to be

Pain disabilityImmediately after the intervention (at 30 minutes)

Measured using the Neck Disability Questionnaire (range: 0-50 and higher scores are indicative of more disability)

AnxietyImmediately after the intervention (at 30 minutes)

Measured using the State-Trait Anxiety Scale, which consists of 2 sub-scales, one measures trait anxiety and the other measures state anxiety; both scales have an independent score that ranges from 20 to 80 and higher scores are indicative of higher anxiety.

CatastrophyzingImmediately after the intervention (at 30 minutes)

Measured using the Pain Catastrophyzing Scale (range: 0-52 and higher scores and indicative of higher pain catastrophyzing)

Trial Locations

Locations (1)

Clínica de Diagnóstico e Terapêutica - Hellman, Lda

🇵🇹

Figueira Da Foz, Portugal

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