Skip to content

Real-time Ultrasound Imaging as Feedback for Deep Cervical Extensors Activation

Real-time Ultrasound Imaging as Feedback for Deep Cervical Extensors Activation

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04201483
Enrollment
30
Registered
2019-12-17
Start date
2019-12-05
Completion date
2020-04-20
Last updated
2019-12-17

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

Conditions

Neck Disorder

Brief summary

The aim of this study will be to determine the value of adding real-time ultrasound imaging (RUSI) as an external feedback tool for teaching the contraction of the deep cervical extensors (DCE) in healthy subjects. The potential benefit of RUSI to facilitate activation of the DCE during a specific motor task as well as the retention capacity of this motor task after a short period of training will be investigated

Detailed description

Participants will be randomly allocated into two exercise groups: DCE exercise without RUSI feedback (DCE) and DCE exercise with RUSI feedback (DCE+RUSI). Participants assigned to DCE will perform an exercise known to selectively activate the semispinalis cervicis muscles. By the other hand, participants in the DCE+RUSI group will perform the same exercise as the DCE group to selectively activate the semispinalis cervicis muscle but receiving RUSI feedback about correct performance. In both groups, a total of 10 sets of 10 repetitions will be performed with one minute of rest between each set. Ultrasound measurement will be used to asses the antero-posterior dimension (thickness) of the DCE both at rest and during contraction at the level of C4 at baseline, immediately after the DCE exercise activation protocol and one-week follow-up in order to evaluate retention capacity. All participants will be asked to not perform any other cervical motor control exercise or exercise using RUSI feedback until the last time point assessment will be finished. All participants will be asked to avoid any exercises or treatments for neck pain between sessions. All ultrasound images will be analysed off-line using Image J software. Thickness and percent thickness change will be measured. The percent thickness change will be calculated by using the following equation: thickness contracted - thickness rest / thickness rest.

Interventions

OTHERDCE without RUSI feedback

Participants assigned to this group will perform an exercise known to selectively activate the semispinalis cervicis muscle

OTHERDCE + RUSI feedback about performance

Participants in this group will perform the same exercise as the DCE group to selectively activate the semispinalis cervicis muscle but receiving RUSI feedback about correct performance

Sponsors

University of Valencia
Lead SponsorOTHER

Study design

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

Masking description

Ultrasound measurements will be performed by the rater responsible of performing ultrasound measurements who will be blinded to the assigned group

Intervention model description

This will be a randomized clinical trial, with parallel groups and a blinded assessor performed in accordance with CONSORT guidelines. Participants will be randomized into two exercise groups: DCE exercise without RUSI feedback (DCE) and DCE exercise with RUSI feedback (DCE+RUSI). Randomization will be conducted using computer-generated random numbers (Epidat® version 3.1). Allocation concealment will be ensured using opaque and sealed envelopes

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* No actual neck pain * Being able to understand Spanish language

Exclusion criteria

* Neck pain in the last 3 months * Previous surgery in the neck region * Neurological diseases or any other condition that may alter voluntary muscle contraction * Previous experience with cervical motor control training exercises * Previous experience using RUSI as an external feedback tool in any other body area

Design outcomes

Primary

MeasureTime frameDescription
Deep cervical extensors function at baselineBaselineUltrasound measurements will be used to asses the antero-posterior dimension (thickness) of the deep cervical extensors both at rest and during contraction at the level of C4
Change of the deep cervical extensors function from baseline to immediately after interventionFrom baseline to immediately after interventionUltrasound measurements will be used to asses the antero-posterior dimension (thickness) of the deep cervical extensors both at rest and during contraction at the level of C4
Change of the deep cervical extensors function from baseline to one week after interventionFrom baseline to one week after interventionUltrasound measurements will be used to asses the antero-posterior dimension (thickness) of the deep cervical extensors both at rest and during contraction at the level of C4

Countries

Spain

Outcome results

None listed

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