Attentional Focus Influence During Cranio-Cervical Flexion Test
NCT ID: NCT03567122
Last Updated: 2019-07-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
90 participants
INTERVENTIONAL
2018-08-01
2019-04-01
Brief Summary
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Detailed Description
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Subjects will be randomized into three groups: Internal focus of attention, external focus of attention and control group.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Internal Focus of Attention
30 subjects will be randomized to this arm. Only internal focus of attention feedback instructions will be given during the execution and training performing the Cranio-Cervical Flexion Test. The subjects allocated to this arm will not be allowed to use the visual feedback traditionally provided during the Cranio-cervical Flexion Test.
Internal Focus of Attention
Information already included in arm/group descriptions.
External Focus of Attention
30 subjects will be randomized to this arm. Only external focus of attention feedback instructions will be given during the execution and training performing the Cranio-Cervical Flexion Test. The subjects allocated to this arm will not be allowed to use the visual feedback traditionally provided during the Cranio-cervical Flexion Test. In addition, they will use just a laser point attached to the head to guide their cranio-cervical flexion.
External Focus of Attention
Information already included in arm/group descriptions.
Control
30 subjects will be randomized to this arm. The participants allocated to this arm will be instructed as traditionally during the Cranio-Cervical Flexion Test. They will be given visual feedback while have their attention guided to the inner neck movement.
Control
Information already included in arm/group descriptions.
Interventions
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Internal Focus of Attention
Information already included in arm/group descriptions.
External Focus of Attention
Information already included in arm/group descriptions.
Control
Information already included in arm/group descriptions.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Historic of trauma/surgery to the cervical or thoracic spine or upper limbs
* Temporomandibular pain
* Neurological or systemic disorder
18 Years
60 Years
ALL
Yes
Sponsors
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Federal University of Health Science of Porto Alegre
OTHER
Responsible Party
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Francisco Xavier de Araujo, Pt
Principal Ivestigator
Principal Investigators
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Marcelo Faria, PhD, PT
Role: STUDY_DIRECTOR
Professor, Researcher
Locations
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Universidade Federal de Ciências da Saúde
Porto Alegre, Rio Grande do Sul, Brazil
Countries
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Other Identifiers
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MSS_ME_01
Identifier Type: -
Identifier Source: org_study_id
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