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Not yet recruiting NCT06028308

The Effect of Adding Auditory Information on Head Movements in People With Traumatic Neck Pain

No phase Interventional Whiplash Healthy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Smartphone playing a sound.
Who it may be relevant to
Registry conditions: Whiplash, Healthy. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study sets out to investigate the potential effect of auditory disturbances on human movement

Detailed description

Clinicians routinely investigate/test human movement but if/how this is effect by auditory disturbances is unclear. This study sets out to investigate the impact of auditory disturbances on head movements.

Interventions

  • Device Smartphone playing a sound
    A sound will be played from a portable device (smartphone mounted with earphones) during movement

Primary outcome measures

  • Range of motion [Time frame: During a single test session (approximately 45minutes) at day 1]
Secondary outcome measures (5)
  • Head repositioning accuracy [Time frame: During a single test session (approximately 45minutes) at day 1]
  • Quality of head movement [Time frame: During a single test session (approximately 45minutes) at day 1]
  • Perceived stiffness during movement [Time frame: During a single test session (approximately 45minutes) at day 1]
  • Perceived difficultness of performing movement [Time frame: During a single test session (approximately 45minutes) at day 1]
  • Perceived neck pain intensity [Time frame: During a single test session (approximately 45minutes) at day 1]

Eligibility criteria

Control group:

Inclusion Criteria (Control):

  • Able to speak, read and understand Danish/English

Exclusion Criteria (Control):

  • Pain from the neck or shoulder area during the past 6 months
  • Experience of delayed onset muscle soreness (DOMS) during the week leading up to the test session
  • Former surgery in neck or shoulder
  • Current or previous chronic or recurrent pain condition that could affect the results
  • Pregnancy
  • Drug addiction defined as the use of cannabis, opioids or other drugs
  • Previous neurologic, musculoskeletal or mental illnesses that could affect the results
  • Regular use of analgesics
  • Abnormally disrupted sleep in the last 24 hours preceding the experiment
  • Lack of ability to cooperate

Neck pain group:

Inclusion Criteria (Neck Pain):

  • Traumatic onset of neck pain
  • Able to speak, read and understand Danish/English
  • Reduced/painful active range of motion of the head and/or painful reaction to palpation of the neck at the time of inclusion

Exclusion Criteria (Neck Pain):

  • Experience of DOMS during the week leading up to the test session
  • Former surgery in neck or shoulder
  • Pregnancy
  • Drug addiction defined as the use of cannabis, opioids or other drugs
  • Previous neurologic, musculoskeletal (other than neck pain) or mental illnesses that could affect the results
  • Abnormally disrupted sleep in the 24 hours preceding the experiment
  • Lack of ability to cooperate

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Basic science

Study locations

Denmark · 2 centers
  • FysioDanmark Aalborg — Aalborg
  • Dept. Of Health Science and Technology, Aalborg University — Gistrup

Identifiers

NCT: NCT06028308 · AAU031-1025976b

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗