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Visual Feedback in Chronic Neck Pain

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03493334
Enrollment
42
Registered
2018-04-10
Start date
2018-04-15
Completion date
2018-06-30
Last updated
2018-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

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).

Interventions

Visual feedback of the neck will be given to participants using two mirrors while performing neck movements.

Participants will be asked to perform active movements of their neck with the mirrors covered.

Sponsors

Aveiro University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Neck pain intensityBaselineMeasured using a 10 cm visual analogue scale

Secondary

MeasureTime frameDescription
Time for pain to return to baseline levelsImmediately after the intervention (at 30 minutes)Measured with a chronometer
Pain disabilityBaselineMeasured using the Neck Disability Questionnaire (range: 0-50 and higher scores are indicative of more disability)
Neck range of motionBaselineMeasured using a goniometer
Pain locationBaselineMeasured using a body chart
CatastrophyzingBaselineMeasured using the Pain Catastrophyzing Scale (range: 0-52 and higher scores and indicative of higher pain catastrophyzing)
AnxietyBaselineMeasured 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.
Neck perceptionBaselineAssessed by asking participants to draw their neck as they perceive it to be
KinesiophobiaBaselineMeasured using the Tampa Scale of Kinsesiophobia (Range: 13-52 and higher values are indicative of a higher fear of movement.

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026