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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04615598
Other study ID # uammadrid91
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 15, 2020
Est. completion date September 30, 2021

Study information

Verified date October 2020
Source Universidad Autonoma de Madrid
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective is to evaluate the effects of action-observation training on tongue strength in brain-damaged patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date September 30, 2021
Est. primary completion date July 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Age between 18 and 70 - Date of injury : 6 months onwards - Medical diagnosis: brain damage or head trauma - Clinical diagnosis of dysphagia by videofluoroscopy or V-CAM and expert opinion. Exclusion Criteria: - Not understanding verbal or auditory/visual commands through the Boston Test - Present behavioural alterations - Presence of seizures - Presence of tracheotomy - Impulsivity - Attention Problems

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Action observation
The idea is to show some videos with the aim of improving patients' tongue strength.
Placebo group
The idea is to show some videos of vegetation with the aim of having an intervention time but ineffective.

Locations

Country Name City State
Spain CSEU La Salle Madrid

Sponsors (2)

Lead Sponsor Collaborator
Universidad Autonoma de Madrid Centro Universitario La Salle

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lingual strength The IOPI instrument has a mechanical sensor that evaluates the force. Change in immediately at the end of the intervention and also, changes between the end and three months
Secondary Cervical Range of motion The cervical goniometer will measure the active cervical range of motion Change in immediately at the end of the intervention and also, changes between the end and three months
See also
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