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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06159426
Other study ID # NEUROUSAL04/2023
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 10, 2023
Est. completion date February 1, 2024

Study information

Verified date December 2023
Source University of Salamanca
Contact Juan Luis Sánchez González, PhD
Phone +34 660 738 949
Email juanluissanchez@usal.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomized clinical trial on a cohort of healthy subjects of legal age, of both sexes, recruited from the university community and who will be randomly distributed into two groups (expert therapist vs. non-expert therapist). The objective will be to determine if there are differences in the muscular activation produced on the stabilizing muscles of the trunk (external oblique and internal oblique) if it is applied by an expert therapist versus if it is applied by a therapist not specialized in therapy and to know the effects produced on the muscles studied after performing the intervention.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date February 1, 2024
Est. primary completion date February 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Over 18 years old. - 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. - Vaccinated in the 10 days prior to the intervention - Fever

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vojta Therapy
The subject will be placed on a stretcher with the torso uncovered. Once the adhesive electrodes have been placed in the different recording areas on the anterior part of the trunk, a recording of the activity at rest will begin, two minutes of stimulation (digital pressure), one minute of rest, two minutes of stimulation in the contralateral side and, finally, one minute of rest. 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. Change from Baseline electromyographic activity at 7 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 kilograms. Baseline
See also
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Not yet recruiting NCT05785962 - Electromyographic Control of the Response in the Application of Vojta Therapy in People With Brain Injury. N/A
Completed NCT04818879 - Abdominal Electromyographic Control in Vojta Therapy N/A