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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06255600
Other study ID # HD-tDCS/Chlorella
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 10, 2021
Est. completion date June 28, 2024

Study information

Verified date March 2024
Source Federal University of Paraíba
Contact Suellen Andrade, PhD
Phone +55(83)986046032
Email suellenandrade@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Recent investigations have shown that of the patients who were affected by SARCov2 have remained with persistent symptoms in a high proportion. In these considerations, the literature has suggested nomenclatures such as "post-COVID-19" and "chronic COVID-19", "long -COVID" and Post-Covid Syndrome for patients recovered from SARCov2 reporting persistent symptoms and signs for weeks to months after resolution of the acute infection. Furthermore, there may be cardiovascular complications in affected patients, the consequences of which can lead to muscle contractility disorders, vascular insufficiency, cardiac arrest, reinforcing the need for controlled, randomized studies, as well as follow-up and monitoring of these. Furthermore, cardiovascular diseases (CVD) are part of the health problems that lead to the most deaths in the world, they also lead to a high proportion of hospital admissions, due to the worsening of the pathology and a higher incidence in the elderly population. The worsening of CVD conditions leads to inadequate food consumption at the hospital level, causing changes in several nutrients, including vitamin B12. The reduction in B12 levels leads to changes in several systems, including the cardiovascular system, and due to the increase in homocysteine and the triggering of the inflammatory cascade. Studies indicate that B12 supplementation through Chlorella (microalgae - functional food) reduced cardiovascular risk and modulated the inflammatory cascade. In combination, neurostimulation has presented aspects that promote pain neuromodulation, due to the improvement of respiratory patterns and inflammatory modulation. More specifically, there is a protocol with promoting findings, this being HD-tDCS. In this sense, this research aims to evaluate the effects of HD-tDCS and the consumption of Chlorella Pyrenoidosa to improve B12 levels in patients with cardiovascular risk post-COVID-19.


Description:

This study is an open label research, clinical trial, double blind, placebo controlled, and randomized, involving assistance to patients at risk of cardiovascular disease, in outpatient care (Continue Caring Project). Included in the research are adults and elderly participants at cardiovascular risk, whose initial diagnosis for hospitalization was due to COVID-19 and at the hospital level those admitted for treatment in the Intensive Care Unit or ward with heart disease who are eligible for neurostimulation by HD-tDCS. Patients will be randomly allocated into an experimental and control group for HD-tDCS and also to receive the functional food. The protocol will be HD-tDCS (lasting 20 minutes of 4x1 tDCS-HD) positioning the central electrode in the left primary motor cortex (M1) with anodal stimulus, twice a week; nutritional monitoring; collection of laboratory tests (at the beginning and end of treatment) and the group that will receive the functional food will be provided with 10 tablets of Chlorella Pyrenoidosa (5g/day) containing 4mcg of B12, organic pressed into tablets (Registration with ANVISA/MS : 6,7273,000) for five weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 28, 2024
Est. primary completion date June 28, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with cardiovascular diagnosis or risk; - Adults and elderly people (18 to 80 years old); - Able to respond to commands and grant consent to participate in the research through the informed consent form; - Who have post-COVID symptoms. Exclusion Criteria: - Patients with a clinical history of neuromuscular or cognitive instability, pregnancy and contraindications for receiving neurostimulation (such as cardiac pacemakers and metallic brain implants); - Patients with contraindications to the use of Chlorella (gastritis, esophagitis, peptic ulcers), - Pregnant patients, patients with stroke and tumors

Study Design


Related Conditions & MeSH terms


Intervention

Other:
High Definition-transcranial Direct Current Stimulation
High-Definition transcranial Direct Current Stimulation (HD-tDCS) is a neuromodulation technique, is non-invasive, targeted, safety.
Dietary Supplement:
Chlorella Pyrenoidosa
functional food, organically pressed into tablets (Registration with ANVISA/MS: 6.7273.000)

Locations

Country Name City State
Brazil Vanessa Meira Cintra João Pessoa Paraíba

Sponsors (2)

Lead Sponsor Collaborator
Federal University of Paraíba City University of New York

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change B12 by blood analysis biochemical Change B12 (above 148pmol/L) After five week of the group of research start
Secondary Change Methylmalonic Acid and Homocysteine Change blood levels of Methylmalonic Acid and Homocysteine (below 270nmol/L and 12mmol/L, respectively) After five week of the group of research start
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