Effects of the Application of a Reflex Locomotion Program in the Neurological Hand

NCT ID: NCT03890965

Last Updated: 2020-04-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-29

Study Completion Date

2019-09-25

Brief Summary

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The recovery of the function of the hand is one of the most important aspects for patients who have suffered the consequences of neurological damage. Currently there are numerous therapeutic procedures aimed at rehabilitation that have scientific evidence such as restrictive therapy. However, dysfunction of the upper limb has an impact on the whole body that is not always taken into consideration.

Detailed Description

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The intervention of the stimulation of the reflex locomotion is carried out in this study in a sitting position in a conventional chair, an unorthodox posture in the usual treatment of Vojta therapy.

Description of the sitting posture: the back in axial extension with the shoulders located in front of the hips.

The elbows must be supported with the medial epicondyl in contact on a table, whose height is at the level of the end of the patient's sternum.

The forearms are placed prone with the palms facing the surface. In this position we place a rubber sphere 3 centimeters in diameter under the pisiform of one of the patient's wrists.

The reflex stimulation is performed by the passive pressure exerted by the weight of the wrist (pisiform) on the rubber sphere. Simultaneously the patient has to exert a slight pressure with the heel towards the ground with his foot. This foot will be the opposite of the wrist that has the sphere under the pisiform.

It is a cross-stimulation, that is, pisiform in one hand together with the load in the heel of the opposite side.

Alternating each diagonal 4 times, 5 minutes each. Total session 20 minutes, 2 times per day, every day according to degree of affectation

The duration of the study will depend on the degree of involvement: mild 2 weeks, moderate 3 months.

Conditions

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Neurological Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Pretest-posttest trial
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Experimental

Adult patients with chronic sequelae in the upper limb after neurological damage

Group Type EXPERIMENTAL

Reflex locomoction therapy

Intervention Type OTHER

The intervention of the stimulation of the reflex locomotion is carried out in this study in a sitting position in a conventional chair, an unorthodox posture in the usual treatment of Vojta therapy.

The reflex stimulation is performed by the passive pressure exerted by the weight of the wrist (pisiform) on the rubber sphere. Simultaneously the patient has to exert a slight pressure with the heel towards the ground with his foot. This foot will be the opposite of the wrist that has the sphere under the pisiform.

Alternating each diagonal 4 times, 5 minutes each. Total session 20 minutes, 2 times x day, every day according to degree of affectation.

Interventions

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Reflex locomoction therapy

The intervention of the stimulation of the reflex locomotion is carried out in this study in a sitting position in a conventional chair, an unorthodox posture in the usual treatment of Vojta therapy.

The reflex stimulation is performed by the passive pressure exerted by the weight of the wrist (pisiform) on the rubber sphere. Simultaneously the patient has to exert a slight pressure with the heel towards the ground with his foot. This foot will be the opposite of the wrist that has the sphere under the pisiform.

Alternating each diagonal 4 times, 5 minutes each. Total session 20 minutes, 2 times x day, every day according to degree of affectation.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Sequelae in the upper limb after neurological damage.
* Understanding and oral expression preserved.
* More than a year after the episode.
* Possibility of walking

Exclusion Criteria

* Aphasia.
* Concomitant diseases: Diabetes and arthritis of the hand.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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NUMEN Foundation

OTHER

Sponsor Role lead

Responsible Party

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Luis Perales Lopez

Physiotherapy service coordinator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Luis Perales Lopez, Doctor

Role: PRINCIPAL_INVESTIGATOR

NUMEN Foundation

Locations

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NUMEN Foundation

Madrid, EspaƱa, Spain

Site Status

Countries

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Spain

Other Identifiers

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NUMEN1

Identifier Type: -

Identifier Source: org_study_id

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