Motor Imagery and Action Observation in Respiratory Training
Effects of Motor Imagery and Action Observation on Respiratory Parameters
1 other identifier
interventional
30
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2023
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 5, 2022
CompletedFirst Posted
Study publicly available on registry
December 22, 2022
CompletedStudy Start
First participant enrolled
January 5, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 4, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
March 5, 2023
CompletedDecember 22, 2022
December 1, 2022
1 month
December 5, 2022
December 14, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Change from Forced vital capacity physiological parameter
With spirometry
Preintervention and postintervention (after the 10 minutes intervention)
Change from FEV1 physiological parameter
With spirometry
Preintervention and postintervention (after the 10 minutes intervention)
Study Arms (3)
Motor imagery
EXPERIMENTALMotor imagery of inspiratory and expiratory exercises, 10 series of 1 minute.
Action observation
EXPERIMENTALAction observation of inspiratory and expiratory exercises, 10 series of 1 minute.
Placebo Observation
PLACEBO COMPARATORPlacebo visualization of nature video, 10 minutes.
Interventions
Eligibility Criteria
You may qualify if:
- Age between 18 and 60
- Healthy and with no respiratory pathology subjects
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
December 5, 2022
First Posted
December 22, 2022
Study Start
January 5, 2023
Primary Completion
February 4, 2023
Study Completion
March 5, 2023
Last Updated
December 22, 2022
Record last verified: 2022-12