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Accepted for/Published in: JMIR Research Protocols

Date Submitted: Mar 9, 2022
Date Accepted: Apr 12, 2023
Date Submitted to PubMed: Jun 7, 2023

The final, peer-reviewed published version of this preprint can be found here:

Evaluation of Lactobacillus Coryniformis K8 Consumption by Health Care Workers Exposed to COVID-19 (LactoCor2 Project): Protocol for a Randomized Controlled Trial

Rodríguez-Blanque R, Sánchez-García JC, Cobos Vargas A, Leyva Martínez MS, Martínez Diz S, Cortés-Martín J, Tovar-Gálvez MI

Evaluation of Lactobacillus Coryniformis K8 Consumption by Health Care Workers Exposed to COVID-19 (LactoCor2 Project): Protocol for a Randomized Controlled Trial

JMIR Res Protoc 2023;12:e37857

DOI: 10.2196/37857

PMID: 37285326

PMCID: 10365585

Evaluation of Lactobacillus coryniformis K8 consumption by healthcare workers exposed to COVID-19 (LactoCor2 Project): Protocol for a randomised controlled trial.

  • Raquel Rodríguez-Blanque; 
  • Juan Carlos Sánchez-García; 
  • Angel Cobos Vargas; 
  • M. Socorro Leyva Martínez; 
  • Silvia Martínez Diz; 
  • Jonathan Cortés-Martín; 
  • María Isabel Tovar-Gálvez

ABSTRACT

Background:

Lactobacillus coryniformis K8 CECT5711 has immune modulating properties, enhances the immune response to viral antigens leading to the production of specific antibodies, has anti-inflammatory activity which may help to prevent uncontrolled inflammatory processes leading to respiratory and other organ failure.

Objective:

To evaluate the effect of the consumption of a probiotic strain on the incidence and severity of COVID-19 in health personnel who carry out their professional work among patients with infection or suspected infection by SARS CoV-2.

Methods:

This is a double-blind randomized clinical trial in which the experimental group will receive a capsule of Lactobacillus K8 per day (3x109 cfu/day) and the control group will receive a daily placebo capsule consisting of maltodextrin. A sample size of 314 volunteers was calculated. Volunteers must meet the following inclusion criteria: over 20 years of age, active health personnel caring for patients with COVID-19, including all professionals such as medical doctors, nurses and caretakers at the two referral hospitals that treat COVID-19 cases. The main outcome of the clinical trial will be the incidence of symptomatic infection by SARS CoV-2 in personnel who care for patients with suspected or confirmed COVID-19.

Results:

The study had to be extended to the two referral hospitals that treat COVID-19 cases in the province of Granada (Andalusia, Spain); Hospital San Cecilio and Hospital Virgen de las Nieves. A total of 255 subjects met the inclusion criteria and were randomly assigned to one of the two groups.

Conclusions:

The results of this RCT will provide valuable information regarding the administration of Lactobacillus K8 against COVID-19, including whether there are fewer infectious processes due to this virus or, in case of occurrence, whether the disease is milder in subjects taking the probiotic strain. Clinical Trial: Clinicaltrials.gov NCT04366180, http://clinicaltrials.gov/ct2/show/NCT04366180).


 Citation

Please cite as:

Rodríguez-Blanque R, Sánchez-García JC, Cobos Vargas A, Leyva Martínez MS, Martínez Diz S, Cortés-Martín J, Tovar-Gálvez MI

Evaluation of Lactobacillus Coryniformis K8 Consumption by Health Care Workers Exposed to COVID-19 (LactoCor2 Project): Protocol for a Randomized Controlled Trial

JMIR Res Protoc 2023;12:e37857

DOI: 10.2196/37857

PMID: 37285326

PMCID: 10365585

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