Electromyographic Control of the Response in the Application of Vojta Therapy in People With Brain Injury.

Not Applicable

Not yet recruiting

• Conditions: Abdominal Muscles

• Registration Number: NCT05785962
• Lead Sponsor: University of Salamanca

Brief Summary

A non-randomized clinical trial on a cohort of healthy subjects of legal age, both sexes, recruited from the university community and who will be randomly distributed into two groups (experimental and control). The objective will be to determine the feasibility of the standardized intervention protocol on the stabilizing muscles of the trunk (external oblique and internal oblique) before, during and after the application of Vojta Therapy, and to know the effects produced on the Musculature studied after performing the intervention.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-03-09
• Study First Submitted QC: 2023-03-23
• Study First Posted: 2023-03-27
• Status Verified: 2024-01
• Last Update Submitted: 2024-01-19
• Last Update Posted: 2024-01-22
• Study Start: 2024-02-01
• Primary Completion: 2024-12-30
• Study Completion: 2025-01-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Not provided

Exclusion Criteria

• Over 80 years
• Healthy people

Group without brain damage

Inclusion Criteria :

• Over 18 and under 80 years of age
• Healthy people
• Full cognitive capacity.

Exclusion Criteria:

• Subjects with neuro-muscular pathologies that affect the abdominal muscles, previous surgeries in the area or any chronic neurological or organic disorder that may alter the results.
• Fever

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Electromyographic activity in abdominal muscles	Change from Baseline electromyographic activity at 10 minutes.	The electromyographic activity of internal and external obliques in nanovolts will be collected before, during and after the intervention. Acquired signals are sampled at 1 KHz and filtered with a 60 Hz high pass digital filter to reject signals of non-muscular origin. The degree of muscle activation measured in micro volts (uV) will be recorded.

Secondary Outcome Measures

Name	Time	Method
Sex	Baseline	It will be registered at the beginning of the study.
Height	Baseline	It will be registered at the beginning of the study in centimeters.
Date of birth	Baseline	It will be registered at the beginning of the study in order to calculate the age of the participant.
Weight	Baseline	It will be registered at the beginning of the study in centimeters.