Motor Imagery and Action Observation in Respiratory Training

NCT ID: NCT05662072

Last Updated: 2022-12-22

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

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-05

Study Completion Date

2023-03-05

Brief Summary

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The principal aim of this study was to asses the effects of motor imagery and action observation training on ventilatory and functional capacity through a randomized controlled trial.

Detailed Description

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Conditions

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Respiratory Function Motor Imagery Action Observation Training

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Motor imagery

Motor imagery of inspiratory and expiratory exercises, 10 series of 1 minute.

Group Type EXPERIMENTAL

Motor imagery

Intervention Type BEHAVIORAL

Mental imagery of respiratory exercises

Action observation

Action observation of inspiratory and expiratory exercises, 10 series of 1 minute.

Group Type EXPERIMENTAL

Action observation

Intervention Type BEHAVIORAL

Action observation of respiratory exercises

Placebo Observation

Placebo visualization of nature video, 10 minutes.

Group Type PLACEBO_COMPARATOR

Placebo Intervention

Intervention Type OTHER

Placebo observation

Interventions

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Motor imagery

Mental imagery of respiratory exercises

Intervention Type BEHAVIORAL

Action observation

Action observation of respiratory exercises

Intervention Type BEHAVIORAL

Placebo Intervention

Placebo observation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age between 18 and 60
* Healthy and with no respiratory pathology subjects

Exclusion Criteria

* Any cognitive impairment that hindered viewing of audiovisual material.
* Difficulty understanding or communicating.
* Presence of systemic pathology, Central Nervous System or rheumatic disease.
* Inadequate understanding of the Spanish language to follow instructions for measuring and treatment.
* Collaboration of pregnant women.
* Underage subject
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cardenal Herrera University

OTHER

Sponsor Role lead

Responsible Party

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Luis Suso

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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luis suso, PhD

Role: CONTACT

Phone: +34627819667

Email: [email protected]

Other Identifiers

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2

Identifier Type: -

Identifier Source: org_study_id