Skip to main content
Clinical Trials/NCT03567122
NCT03567122
Completed
Not Applicable

Attentional Focus Influence During Cranio-Cervical Flexion Test

Federal University of Health Science of Porto Alegre1 site in 1 country90 target enrollmentAugust 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neck; Anomaly
Sponsor
Federal University of Health Science of Porto Alegre
Enrollment
90
Locations
1
Primary Endpoint
Change from baseline in Electromyographic Activity of Sternocleidomastoid
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to termine if a different attentional focus would alter the motor control in cervical muscles during the cranio-cervical test.

Detailed Description

Asymptomatic subjects will be recruited to this study. Superficial electromyography of the Sternocleidomastoid, Range of Motion (ROM) and Cranio-Cervical Flexion Test (CCFT) will be measured before, immediately after change in focus of attention, 2 days after training under a particular focus of attention, and 7 days after training the task under the same focus of attention. Subjects will be randomized into three groups: Internal focus of attention, external focus of attention and control group.

Registry
clinicaltrials.gov
Start Date
August 1, 2018
End Date
April 1, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Federal University of Health Science of Porto Alegre
Responsible Party
Principal Investigator
Principal Investigator

Francisco Xavier de Araujo, Pt

Principal Ivestigator

Federal University of Health Science of Porto Alegre

Eligibility Criteria

Inclusion Criteria

  • Asymptomatic subjects

Exclusion Criteria

  • Cervical pain
  • Historic of trauma/surgery to the cervical or thoracic spine or upper limbs
  • Temporomandibular pain
  • Neurological or systemic disorder

Outcomes

Primary Outcomes

Change from baseline in Electromyographic Activity of Sternocleidomastoid

Time Frame: Baseline, Immediately after baseline, Post-Training (2 days after the baseline), Retention (7 days after finished training)

The Electromyography (EMG) signal amplitude will be determined by the root mean square (RMS) value computed over intervals of 1 s during each 10-s contraction. RMS will be expressed as a percentage of the maximum RMS value during the reference voluntary contraction.

Secondary Outcomes

  • Cranio-cervical Range of Motion(Baseline, Immediately after baseline, Post-Training (2 days after the baseline), Retention (7 days after finished training))
  • Cranio-Cervical Flexion Test Performance(Baseline, Immediately after baseline, Post-Training (2 days after the baseline), Retention (7 days after finished training))

Study Sites (1)

Loading locations...

Similar Trials