Effects of Action Observation and Motor Imagery on Orofacial Sensorimotor Variables

NCT ID: NCT04022174

Last Updated: 2019-07-22

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-07-12

Study Completion Date

2019-08-15

Brief Summary

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The main objective of the present study was to evaluate the effects of different dosages of action observation (AO) and motor imagery (MI) combined with an orofacial exercise program on pain pressure thresholds, lingual endurance and perceived exertion in asymptomatic subjects.

Detailed Description

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Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Moderate dosage training

Group Type EXPERIMENTAL

Moderate dosage training of action Observation and Motor imagery

Intervention Type BEHAVIORAL

Motor imagery and action observation of orofacial exercises with moderate dosage

Moderate dosage orofacial exercises

Intervention Type BEHAVIORAL

Orofacial exercises with moderate intensity

Intensive dosage training

Group Type EXPERIMENTAL

Intensive dosage training of action observation and motor imagery

Intervention Type BEHAVIORAL

Motor imagery and action observation of the orofacial exercises with intensive dosage

Intensive dosage orofacial exercises

Intervention Type BIOLOGICAL

Orofacial exercises with high intensity

Interventions

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Moderate dosage training of action Observation and Motor imagery

Motor imagery and action observation of orofacial exercises with moderate dosage

Intervention Type BEHAVIORAL

Intensive dosage training of action observation and motor imagery

Motor imagery and action observation of the orofacial exercises with intensive dosage

Intervention Type BEHAVIORAL

Intensive dosage orofacial exercises

Orofacial exercises with high intensity

Intervention Type BIOLOGICAL

Moderate dosage orofacial exercises

Orofacial exercises with moderate intensity

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. healthy individuals with no pain
2. aged between 18 and 65 years
3. subjects with correct masticatory function and labial and lingual mobility

Exclusion Criteria

1. individuals who presented systemic, cardiorespiratory, central nervous system or rheumatic diseases, or those who presented any musculoskeletal or craniocervical pathology
2. underage individuals
3. individuals with orofacial pain or temporomandibular disorders at the time of the study
4. subjects' complaint of toothache or tenderness to percussion.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad Autonoma de Madrid

OTHER

Sponsor Role lead

Responsible Party

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Roy La Touche Arbizu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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CSEU La Salle

Madrid, , Spain

Site Status

Countries

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Spain

Central Contacts

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Roy La Touche

Role: CONTACT

+349174019803

Luis Suso Marti

Role: CONTACT

627819667

Facility Contacts

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Roy La Touche

Role: primary

917401980

Other Identifiers

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uammadrid10

Identifier Type: -

Identifier Source: org_study_id

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