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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05785962
Other study ID # ElectroVojta
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 1, 2024
Est. completion date January 1, 2025

Study information

Verified date January 2024
Source University of Salamanca
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 1, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Brain injury group Inclusion Criteria : - Over 18 and under 80 years of age - Persons with a medical diagnosis of brain damage secondary to stroke - Have preserved the ability to walk, even with some type of orthopedic some type of orthopedic aid, 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


Related Conditions & MeSH terms


Intervention

Other:
Vojta Therapy
The therapy consists of the application of a stimulating pressure in the pectoral area in the pattern of the locomotion complex of reflex rolling in its first phase. For this, the subject will be placed in a supine position aligned with respect to the axial axis, with the arms along the body, the lower extremities in extension, and the head extended with a rotation of approximately 30º towards one side of the stimulation. The manual stimulation pressure will be exerted in the space between the 6th-7th or the 7th-8th rib under the mammillary line, with a force of about 2 kg.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Salamanca

Outcome

Type Measure Description Time frame Safety issue
Primary Electromyographic activity in abdominal muscles 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. Change from Baseline electromyographic activity at 10 minutes.
Secondary Date of birth It will be registered at the beginning of the study in order to calculate the age of the participant. Baseline
Secondary Sex It will be registered at the beginning of the study. Baseline
Secondary Height It will be registered at the beginning of the study in centimeters. Baseline
Secondary Weight It will be registered at the beginning of the study in centimeters. Baseline
See also
  Status Clinical Trial Phase
Recruiting NCT01595165 - Transversus Abdominis Plane Block and Postoperative Pain After Laparoscopic Cholecystectomy N/A
Completed NCT03539211 - Clinical Assessment and Thickness Changes of the Oblique and Multifidus Muscles N/A
Not yet recruiting NCT06159426 - Expert vs. Non-expert Abdominal Electromyographic Control in Vojta Therapy N/A
Completed NCT04818879 - Abdominal Electromyographic Control in Vojta Therapy N/A