Effect of the Vojta Therapy in Patients Multiple Sclerosis
Effect of the Vojta Therapy on Lipid Biomarkers Related to Myelin in Subjects With Multiple Sclerosis.
What it found
A paper reports the results; we have not read it yet. See Papers below.
What was tested
Treatment tested
- Randomized clinical trial.
What it measured
Main measures
Respiratory function
5 minutes
Physical functionSpasticity
10 minutes
SpasticityBalance
10 minutes
Walking and mobilityAge
1 minutes
Time reaction
5 minutes
Other measures (1)
Myelin
15 minutes
How the body handles the medicine
Who could take part
MS (type not specified) · 20 to 65
Show the full criteria
Inclusion criteria
* Persons with MS who have signed the informed consent. * Persons of both sexes. * Ages between 20 and 65 years. * Subjects of both sexes diagnosed with multiple sclerosis on the EDSS (Expanded Disability Status Scale).
Exclusion criteria
* Persons with multiple sclerosis with EDSS scale score equal to or greater than 7.0. * Occurrence of a flare during the period of the patient's participation in the study. * Pregnant women. * Oncology patients. * Non-acceptance and non-signing of informed consent. * Refusal to participate in the study. * Patients with severe cognitive impairment that does not allow them to understand the development of the study. * Patients with cardiovascular instability. * Patients who do not complete at least 75% of the scheduled sessions. Patients who do not present any of the contraindications contemplated for Vojta therapy.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
Multiple sclerosis is the most common disabling neurological disease in young adults. Inflammation, demyelination, neurodegeneration, gliosis and repair processes are involved in its process, which are responsible for the heterogeneity and individual variability in the expression of the disease, the prognosis and the response to treatment. Clinically, MS manifests itself with the following symptoms: sensory focus, motor focus, spasticity, balance disorders, visual disturbances such as loss of vision or double vision or sphincter dysfunction. The main subtypes of MS are relapsing-remitting, secondary progressive, primary progressive, and progressive relapsing. Clinically, RRMS presents the initial inflammatory phase, characterized by reversible flares with neurological dysfunction, followed by periods of remission. Approximately 40-50% of these patients progress to SPMS, where the disease gradually progresses from intermittent flare-ups to steadily progressive worsening, resulting in permanent disability due to massive axonal loss. PPMS is the most severe subtype, affecting approximately 10% of all cases, and manifesting as progressive degeneration without any remission.
Papers
Loading reviews and guidelines…
History
Started
Dec 2022
Main results due
Jun 2023
Finished
Dec 2023