COVID-19MDNCT04424940
COVID-19 Lessons Learned: the Outcome of TOMEKA® Project is to Teach
An observational study of COVID-19, run by University of Kinshasa at 1 site in Democratic Republic of the Congo.
Trial summary
Living in Canada and being health-worker in the first line face to COVID-19, investigator outcome is to teach an experience or explain the disease using a review and get people prepared to COVID-19 treatment focused on adherence to the HIV approved 2006-2007 protocol at Ghent University but the review shows an older… Read more about this study
- Who is it for?
- Ages 15 to 75 yearsHealthy volunteers can take part
- Conditions the study is for
- COVID-19
- How many people
- 800 participants
- Where
- 1 siteDemocratic Republic of the Congo
- Study dates
- 1 Sep 2020to 1 Sep 2021
- How long will I take part?
- 9 Months
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 15 to 75 years
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: * Age: 15-75 * Sex: M, F
Who may be able to join
- Fulfill Inclusion criteria and accept
- COVID-19 patients confirmed
- be regular on appointments
Who cannot join
- COVID-19 suspected clinically
- Children
- refuse to participate
Trial locations and contacts
1 site in 1 country.
Democratic Republic of the Congo1 site
Cliniques Universitaires de Kinshasa
Kinshasa, BP KIN XI
GUYGUY K. TSHIMA, Dr., 0015143819264, guyguytshimakabundi@gmail.com
About this study
Official title: TOMEKA® Project Was Sponsored by the University of Kinshasa: it's an Observational Study by Its Reviewed Documentation
Living in Canada and being health-worker in the first line face to COVID-19, investigator outcome is to teach an experience or explain the disease using a review and get people prepared to COVID-19 treatment focused on adherence to the HIV approved 2006-2007 protocol at Ghent University but the review shows an older different study approved at the University of Kinshasa and its ethics approval that again is an old document. So no ethics document supporting the study exists as it is now and no registration. It is an observational study and therefore would not usually require registration in order for the results to be published. It is not a type of secondary literature. The formula TOMEKA® (Mix porridge of maize, sorghum, and soya) follows FOOD + HEALTH CLAIM. It is scientifically justified, relevantly used, and correctly communicated. Methodology: sufficient data? scientific consensus? correct methodology? correct population? context: significant results? context of use, realistic ingestion? correct target group? communication: consumer perception? exaggerated/insinuative, clear, precise, complete, correct information? not misleading? correctly presented? The product TOMEKA® tried to fulfill to above questions in a fitting way with COVID-19 which is an emerging, rapidly evolving situation without a vaccine.
Read the detailed description
On 12/06/2020 worldwide, COVID-19 affected 7 273 958 confirmed cases with 413 372 deaths, 97 894 confirmed in Canada with 8 048 deaths, 53 666 confirmed cases in Quebec with 5 148 deaths, 4 637 confirmed cases with 101 deaths in the Democratic Republic of the Congo where the situation is disastrous: an immense country and the ways of communication are difficult and damaged. It becomes gymnastics to get a drug package.
The principal investigator provide the details of this study to be available to the public in getting knowledge of Covid-19 and micronutrients using the product TOMEKA®.
The individual contribution of ingredients in the nutritional composition of TOMEKA® (mixed flour). Composition of TOMEKA® (Clinical Research Protocol): 100 g of TOMEKA contain 20.1 g of protein; 57.8 g of carbohydrates, 10.1 g of lipids; 8.5 mg iron; 117.6 mg Calcium; 16.6 mg Sodium; 55 μg of Selenium and 378.6 kcal of energy.TOMEKA will be made with soy, maize, sorghum. The above calculations were made with the food composition table (no laboratory analyzes).
Quantity to be served per meal (in g): 30 g for 6-8 months (113,4 Kcal of Energy per served meal). 40 g for 9-11 months (151 Kcal): 50 g for 12-23 months and more expecting to provide 189 Kcal of energy per served per meal. Each group needs 4-5 meals a day to get the equivalent of their daily nutritional needs.
The study will focus on Selenium, a powerful non-enzymatic antioxidant, more powerful than Vit C and Vit E combined. The formula TOMEKA® follows FOOD + HEALTH CLAIM.
A clear device to follow micronutrients and Covid-19 symptoms:
Example 1: Vitamin D and Covid-19 (Press release from the National Academy of Medicine in France May 22, 2020) Vitamin D is a prohormone synthesized in the dermis under the effect of ultraviolet rays, that is to say of the rays of the sun, then transported in the liver and the kidney where it is transformed into an active hormone. It is responsible for the intestinal absorption of calcium and bone health, but vitamin D also has unconventional effects. In particular, it modulates the functioning of the immune system by stimulating macrophages and dendritic cells [1,2,3]. It plays a role in regulating and suppressing the cytokine inflammatory response which causes acute respiratory distress syndrome which characterizes the severe and often lethal forms of Covid-19. A significant correlation between low serum vitamin D levels and mortality by Covid-19 has been shown [4]. This phenomenon generally follows a North-South gradient, although there are exceptions such as the Nordic countries where the supplementation of the nutrients in vitamin D, in particular milk products, is systematic. On the other hand, the countries of southern Europe surprisingly display a high prevalence of vitamin D deficiency despite higher sunshine [5]. This would explain why children who receive vitamin D regularly have asymptomatic forms of Covid-19 and fewer complications. Vitamin D cannot be considered as a preventive or curative treatment for SARS-CoV-2 infection; but by mitigating the inflammatory storm and its consequences, it could be considered as an adjunct to any form of therapy.
The National Academy of Medicine in France recalls that the administration of vitamin D orally is a simple, inexpensive measure and reimbursed by Health Insurance; - confirms its recommendation to ensure vitamin D supplementation in the French population in a report in 2012 [2]; - recommend that the serum vitamin D level (i.e. 25OHD) be measured quickly in people over 60 years of age with Covid-19 and that it be administered in the event of a deficiency, a loading dose of 50,000 to 100,000 IU which could help limit respiratory complications; - recommends providing vitamin D supplementation of 800 to 1,000 IU / day in people under the age of 60 as soon as the diagnosis of Covid-19 is confirmed.
Example 2: Selenium and Covid-19
Now is the time to give extra attention to a balanced diet and assure an optimum dietary micronutrient and vitamin intake! Particularly the micronutrient selenium plays an essential role in antioxidant functioning and helps to alleviate the negative health impacts of viral infections, including inflammation of the lungs (see e.g. https://lnkd.in/eqAGhDH).
Particularly elderly people are often selenium-deficient, which was proven to be the case in e.g. Italy (see https://lnkd.in/epFKVEY). However, when taking micronutrient and vitamin supplements, also follow the instructions to avoid over-supplementation! A healthy and balanced diet is the safest way towards an appropriate dietary micronutrient and vitamin intake.
Description of what investigators will measure:
- The Production of Medical Knowledge:
- Learning medicine:
How it will be measured:
- The Production of Medical Knowledge: Anthropology/Medicine. It is substantial and it showed by the title.
- Learning medicine: The clinical trial shows that medical anthropology connects anthropology and social theory generally with some of the more significant questions of our epoch with the COVID-19 pandemic.
And at what time points it will be measured:
- The Production of Medical Knowledge: the principal investigator has received notifications from Researchgate about 700 researchers who read his research theme, so it deserves to be widely read and taught.
- Learning medicine: This is an original trial, which combines theoretical argument with empirical observation
Objectives:
- Investigators would like the participant to accept the notion that all knowledge is socially and culturally constructed.
- Investigators would examine the contexts in which that knowledge is produced talking on the theme of nutrition in research and aiming to act in medicine, psychiatry, epidemiology, and anthropology.
- Investigators would like the participant acts in behavioral medicine, public health, epidemiology, anthropology as well as .nutrition.
The hypothesis of investigators work:
- Patients with COVID-19 have an increased demand for Selenium
- Selenium supplementation reduces the viral rate
- Selenium supplementation improves the BMI of COVID-19 patients
- Selenium supplementation reduces COVID-19 related morbidity
- Selenium supplementation postponed COVID-19 related mortality
- Selenium supplementation is adjuncted to any form of COVID-19 therapy with nutrition education
- Nutrition education improves health status
- Selenium supplementation and nutrition education should be incorporated into the global Nutritional care and support of COVID-19 patients Methodology: observational study using a questionnaire. Study Population: Age: 15-75 Sex: M, F Inclusion Criteria: Fulfill Inclusion criteria and accept: The participant is asked on the symptoms of the COVID-19 with a questionnaire. If he/she can write yes to any of these questions in order to be tested: In the past 4 hours, have you taken any medicines for fever or headaches, such as acetaminophen (Paracetamol, Tylenol, Tempra), ibuprofen (Advil, Motrin) or Aspirin? Yes No Do you have a thermometer to take your body temperature? Yes No If you don't have a thermometer, do you have any of the following symptoms: warm forehead, muscle or joint pain, chills, general weakness? Yes No In the past 24 hours, have you had trouble breathing or been short of breath? Yes No In the past 24 hours, have you had chest pain? Yes No Do you have a cough? Or if you have a health condition that is causing you to cough, is your cough worse than usual? Yes No In the past 24 hours, have you had a sore throat? Yes No In the past 24 hours, have you had a runny nose? Yes No In the past 24 hours, have you felt a loss of smell (in the absence of nasal congestion)? Yes No In the past 24 hours, have you had diarrhea (three or more bowel movements)? Yes No In the past 24 hours, have you had a headache? Yes No In the past 24 hours, have you felt more tired than usual and unable to carry out your daily activities? Yes No COVID-19 patients confirmed be regular on appointments Exclusion Criteria: COVID-19 suspected clinically Children refuse to participate Initial assessment for the exclusion of suspected Covid-19 cases:
- New or exacerbated cough: Yes/No
- Sore throat: Yes/No
- Fever: Yes/No
- Intestinal gastritis symptoms (Diarrhea, nausea or vomiting): Yes/No
- Anosmia (loss of smell) / Ageusia (loss of taste): Yes/No
- Shortness of breath: Yes/No
- Sputum production: Yes/No
- Weakness: Yes/No
- Headache: Yes/No
- Myalgia / athralgia: Yes/No
- Nasal congestion: Yes/No
- Hemoptysis: Yes/No
- Conjunctivitis: Yes/No Comments: If yes to any of these questions: rule out an acute health condition. If no acute cause identified, consider the person as a probable case and transfer to the warm unit.
- Atypical geriatric signs
- Sudden loss of autonomy (less than 1 week)
- Sudden change in mental state (over 1 week)
- Sudden change in behavior (new behavior or cessation of behavior (less than 1 week)
- Geriatric fever (Oral or rectal temperature greater than or equal to 37.8 C or if increase of 1.1 C compared to the usual normal T)
Other comments:
………………………………………………………………………………………………………….. ........................................................................................................................................................................................................................................................................................................................................................................................................................................................
- Physical examination inspection:
- Assessment of mental state
- Attention span: attentive, not attentive
- State of consciousness: hyper-alert (or agitation), Lethargic (verbal), alert stupor (physical, comatose
- Basic settings:
Vital signs:
Pulse: ……… / min TA: .......... / ……………. T: ................ C (fever if bu oral or rectal sup or equal 37.8 C or if 1.1 C increase compared to the usual normal T)
Breathing:
Frequency: ......... / min
Type: Abdominal chest
Amplitude: normal deep surface
Rhythm: regular irregular
Draw: yes no
Saturation (normal to 94% and +, unless otherwise indicated):
Saturation: ............% ambient AIr With O2 …… ..L / min
- Auscultation:
Anterior side
Abnormal noise: Yes No
Name if possible:
Sibilant
Ronchis
Right bronchus (A)
Left bronchus (B)
Posterior side
Presence of abnormal noise:
Yes
No
Name if possible:
Sibilant
Crackling
Lower right row
Left lower lobe
- Medical decision making
Prescribed screening test (oro-nasopharyngeal sample): yes no
If the sample confirms the presence of COVID-19, isolate the patient in the warm unit.
- Clinical monitoring of COVID-19 confirmed or suspected
Stable patient
Respiratory rate : q 2h and as needed
SpO2 and Temperature: per day and as needed
Blood pressure and Cardiac frequency: per day
Unstable patient (having had an episode of respiratory distress)
Respiratory rate: every hour and as needed
SpO2 and Temperature: per day and as needed
Surname and first name of doctor
Permits
Signature
DD / MM / YYYY
HH: MM
References:
- - Liu PT, Stenger S, et al. Toll like receptor triggering of a vitamin D mediated humanantimicrobial response. Science, 2006, 311 : 1770.
- - Rapport de l'Académie nationale de médecine. Statut vitaminique, rôle extra osseux etbesoins quotidiens en vitamine D. Bull Acad Natle Med. 2012, 196, 1011.
- - Laird E, Rhodes JM and Kenny RA. Vitamin D and inflammation : potential implications for severity of Covid-19. Irish med J, 2020, 113 : 81.
- - McCartney DM, Byrne DG. Optimisation of vitamin D status impact mortality fromSARS -CoV-2 infection Irish Med J .2020 113 : 58.5- Lips P, Cashman KD, et al. Current vitamin D status in European and Middle East countries and strategies to prevent vitamin D deficiency : a position statement of the European Calcified Tissue Society. Eur J Endocrinol, 2019, 180 : P23-P54.
Links:
https://lnkd.in/eqAGhDH https://lnkd.in/epFKVEY
- Conditions
- COVID-19
- Keywords
- TOMEKA®, Treatment, COVID-19, Education
- Medical subject headings
- COVID-19
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of participants with treatment-TOMEKA® usage as assessed by Education
Change people's behaviour
Measured: 9 months
Secondary outcomes (1)
Change From Baseline in nutraceuticals usage on the care of the Covid-19 at 9 months
Change people's behaviour
Measured: 9 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jun 2020
- Study start1 Sep 2020 (estimated)
- Primary completion1 Jun 2021 (estimated)
- Study completion1 Sep 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for COVID-19Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 800 participants (estimated)
- Target duration
- 9 Months
Sponsor and investigators
- Lead sponsor
- University of Kinshasa
- Sponsor type
- University, hospital or other
- Collaborators
- University Ghent, Université de Montréal
- Responsible party
- Principal investigator, Guyguy K Tshima, MD, University of Kinshasa
- Investigators
- GUYGUY KABUNDI TSHIMA, MD, Principal investigator, University of Kinshasa
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04424940
- Sponsor's protocol ID
- UKinshasa
- Other IDs
- Tshima Guyguy Kabundi
- Acronym
- MD
- Status last verified
- Jun 2020
- First submitted
- 20 May 2020
- Last updated
- 16 Jun 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Through researchgate website
Publications
This phenomenon generally follows a North-South gradient, although there are exceptions such as the Nordic countries where the supplementation of the nutrients in vitamin D, in particular milk products, is systematic. On the other hand, the countries of southern Europe surprisingly display a high prevalence of vitamin D deficiency despite higher sunshine
This would explain why children who receive vitamin D regularly have asymptomatic forms of Covid-19 and fewer complications. Vitamin D cannot be considered as a preventive or curative treatment for SARS-CoV-2 infection; but by mitigating the inflammatory storm and its consequences, it could be considered as an adjunct to any form of therapy.
The National Academy of Medicine in France recalls that the administration of vitamin D orally is a simple, inexpensive measure and reimbursed by Health Insurance; - confirms its recommendation to ensure vitamin D supplementation in the French population in a report in 2012 [2]; - recommend that the serum vitamin D level (i.e. 25OHD) be measured quickly in people over 60 years of age with Covid-19, and that it be administered in the event of a deficiency , a loading dose of 50,000 to 100,000 IU which could help limit respiratory complications; - recommends providing vitamin D supplementation of 800 to 1,000 IU / day in people under the age of 60 as soon as the diagnosis of Covid-19 is confirmed.
Now is the time to give extra attention to a balanced diet and assure an optimum dietary micronutrient and vitamin intake! Particularly the micronutrient selenium plays an essential role in antioxidant functioning and helps to alleviate negative health impacts of viral infections, including inflammation of the lungs
Particularly elderly people are often selenium-deficient, which was proven to be the case in e.g. Italy
However, when taking micronutrient and vitamin supplements, also follow the instructions to avoid over-supplementation! A healthy and balanced diet is the safest way towards an appropriate dietary micronutrient and vitamin intake.
Vitamin D is a prohormone synthesized in the dermis under the effect of ultraviolet rays, that is to say of the rays of the sun, then transported in the liver and the kidney where it is transformed into an active hormone. It is responsible for the intestinal absorption of calcium and bone health, but vitamin D also has unconventional effects. In particular, it modulates the functioning of the immune system by stimulating macrophages and dendritic cells.
It plays a role in regulating and suppressing the cytokine inflammatory response which causes acute respiratory distress syndrome which characterizes the severe and often lethal forms of Covid-19. A significant correlation between low serum vitamin D levels and mortality by Covid-19 has been shown.
Study at a glance
From the registry record, last updated by the sponsor on 16 Jun 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- TOMEKA® Project Was Sponsored by the University of Kinshasa: it's an Observational Study by Its Reviewed Documentation
- ClinicalTrials.gov ID
- NCT04424940
- Acronym / sponsor ID
- MD / UKinshasa
- Conditions
- COVID-19
- Keywords
- TOMEKA®, Treatment, COVID-19, Education
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 800 participants (estimated)
- Lead sponsor
- University of KinshasaUniversity, hospital or other
- Collaborators
- University Ghent, Université de Montréal
- Study start
- 1 Sep 2020 (estimated)
- Primary completion
- 1 Jun 2021 (estimated)
- Study completion
- 1 Sep 2021 (estimated)
- First posted
- 11 Jun 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Living in Canada and being health-worker in the first line face to COVID-19, investigator outcome is to teach an experience or explain the disease using a review and get people prepared to COVID-19 treatment focused on adherence to the HIV approved 2006-2007 protocol at Ghent University but the review shows an older different study approved at the University of Kinshasa and its ethics approval that again is an old document. So no ethics document supporting the study exists as it is now and no registration. It is an observational study and therefore would not usually require registration in order for the results to be published. It is not a type of secondary literature. The formula TOMEKA® (Mix porridge of maize, sorghum, and soya) follows FOOD + HEALTH CLAIM. It is scientifically justified, relevantly used, and correctly communicated. Methodology: sufficient data? scientific consensus? correct methodology? correct population? context: significant results? context of use, realistic ingestion? correct target group? communication: consumer perception? exaggerated/insinuative, clear, precise, complete, correct information? not misleading? correctly presented? The product TOMEKA® tried to fulfill to above questions in a fitting way with COVID-19 which is an emerging, rapidly evolving situation without a vaccine.
Detailed description
On 12/06/2020 worldwide, COVID-19 affected 7 273 958 confirmed cases with 413 372 deaths, 97 894 confirmed in Canada with 8 048 deaths, 53 666 confirmed cases in Quebec with 5 148 deaths, 4 637 confirmed cases with 101 deaths in the Democratic Republic of the Congo where the situation is disastrous: an immense country and the ways of communication are difficult and damaged. It becomes gymnastics to get a drug package.
The principal investigator provide the details of this study to be available to the public in getting knowledge of Covid-19 and micronutrients using the product TOMEKA®.
The individual contribution of ingredients in the nutritional composition of TOMEKA® (mixed flour). Composition of TOMEKA® (Clinical Research Protocol): 100 g of TOMEKA contain 20.1 g of protein; 57.8 g of carbohydrates, 10.1 g of lipids; 8.5 mg iron; 117.6 mg Calcium; 16.6 mg Sodium; 55 μg of Selenium and 378.6 kcal of energy.TOMEKA will be made with soy, maize, sorghum. The above calculations were made with the food composition table (no laboratory analyzes).
Quantity to be served per meal (in g): 30 g for 6-8 months (113,4 Kcal of Energy per served meal). 40 g for 9-11 months (151 Kcal): 50 g for 12-23 months and more expecting to provide 189 Kcal of energy per served per meal. Each group needs 4-5 meals a day to get the equivalent of their daily nutritional needs.
The study will focus on Selenium, a powerful non-enzymatic antioxidant, more powerful than Vit C and Vit E combined. The formula TOMEKA® follows FOOD + HEALTH CLAIM.
A clear device to follow micronutrients and Covid-19 symptoms:
Example 1: Vitamin D and Covid-19 (Press release from the National Academy of Medicine in France May 22, 2020) Vitamin D is a prohormone synthesized in the dermis under the effect of ultraviolet rays, that is to say of the rays of the sun, then transported in the liver and the kidney where it is transformed into an active hormone. It is responsible for the intestinal absorption of calcium and bone health, but vitamin D also has unconventional effects. In particular, it modulates the functioning of the immune system by stimulating macrophages and dendritic cells [1,2,3]. It plays a role in regulating and suppressing the cytokine inflammatory response which causes acute respiratory distress syndrome which characterizes the severe and often lethal forms of Covid-19. A significant correlation between low serum vitamin D levels and mortality by Covid-19 has been shown [4]. This phenomenon generally follows a North-South gradient, although there are exceptions such as the Nordic countries where the supplementation of the nutrients in vitamin D, in particular milk products, is systematic. On the other hand, the countries of southern Europe surprisingly display a high prevalence of vitamin D deficiency despite higher sunshine [5]. This would explain why children who receive vitamin D regularly have asymptomatic forms of Covid-19 and fewer complications. Vitamin D cannot be considered as a preventive or curative treatment for SARS-CoV-2 infection; but by mitigating the inflammatory storm and its consequences, it could be considered as an adjunct to any form of therapy.
The National Academy of Medicine in France recalls that the administration of vitamin D orally is a simple, inexpensive measure and reimbursed by Health Insurance; - confirms its recommendation to ensure vitamin D supplementation in the French population in a report in 2012 [2]; - recommend that the serum vitamin D level (i.e. 25OHD) be measured quickly in people over 60 years of age with Covid-19 and that it be administered in the event of a deficiency, a loading dose of 50,000 to 100,000 IU which could help limit respiratory complications; - recommends providing vitamin D supplementation of 800 to 1,000 IU / day in people under the age of 60 as soon as the diagnosis of Covid-19 is confirmed.
Example 2: Selenium and Covid-19
Now is the time to give extra attention to a balanced diet and assure an optimum dietary micronutrient and vitamin intake! Particularly the micronutrient selenium plays an essential role in antioxidant functioning and helps to alleviate the negative health impacts of viral infections, including inflammation of the lungs (see e.g. https://lnkd.in/eqAGhDH).
Particularly elderly people are often selenium-deficient, which was proven to be the case in e.g. Italy (see https://lnkd.in/epFKVEY). However, when taking micronutrient and vitamin supplements, also follow the instructions to avoid over-supplementation! A healthy and balanced diet is the safest way towards an appropriate dietary micronutrient and vitamin intake.
Description of what investigators will measure:
- The Production of Medical Knowledge:
- Learning medicine:
How it will be measured:
- The Production of Medical Knowledge: Anthropology/Medicine. It is substantial and it showed by the title.
- Learning medicine: The clinical trial shows that medical anthropology connects anthropology and social theory generally with some of the more significant questions of our epoch with the COVID-19 pandemic.
And at what time points it will be measured:
- The Production of Medical Knowledge: the principal investigator has received notifications from Researchgate about 700 researchers who read his research theme, so it deserves to be widely read and taught.
- Learning medicine: This is an original trial, which combines theoretical argument with empirical observation
Objectives:
- Investigators would like the participant to accept the notion that all knowledge is socially and culturally constructed.
- Investigators would examine the contexts in which that knowledge is produced talking on the theme of nutrition in research and aiming to act in medicine, psychiatry, epidemiology, and anthropology.
- Investigators would like the participant acts in behavioral medicine, public health, epidemiology, anthropology as well as .nutrition.
The hypothesis of investigators work:
- Patients with COVID-19 have an increased demand for Selenium
- Selenium supplementation reduces the viral rate
- Selenium supplementation improves the BMI of COVID-19 patients
- Selenium supplementation reduces COVID-19 related morbidity
- Selenium supplementation postponed COVID-19 related mortality
- Selenium supplementation is adjuncted to any form of COVID-19 therapy with nutrition education
- Nutrition education improves health status
- Selenium supplementation and nutrition education should be incorporated into the global Nutritional care and support of COVID-19 patients Methodology: observational study using a questionnaire. Study Population: Age: 15-75 Sex: M, F Inclusion Criteria: Fulfill Inclusion criteria and accept: The participant is asked on the symptoms of the COVID-19 with a questionnaire. If he/she can write yes to any of these questions in order to be tested: In the past 4 hours, have you taken any medicines for fever or headaches, such as acetaminophen (Paracetamol, Tylenol, Tempra), ibuprofen (Advil, Motrin) or Aspirin? Yes No Do you have a thermometer to take your body temperature? Yes No If you don't have a thermometer, do you have any of the following symptoms: warm forehead, muscle or joint pain, chills, general weakness? Yes No In the past 24 hours, have you had trouble breathing or been short of breath? Yes No In the past 24 hours, have you had chest pain? Yes No Do you have a cough? Or if you have a health condition that is causing you to cough, is your cough worse than usual? Yes No In the past 24 hours, have you had a sore throat? Yes No In the past 24 hours, have you had a runny nose? Yes No In the past 24 hours, have you felt a loss of smell (in the absence of nasal congestion)? Yes No In the past 24 hours, have you had diarrhea (three or more bowel movements)? Yes No In the past 24 hours, have you had a headache? Yes No In the past 24 hours, have you felt more tired than usual and unable to carry out your daily activities? Yes No COVID-19 patients confirmed be regular on appointments Exclusion Criteria: COVID-19 suspected clinically Children refuse to participate Initial assessment for the exclusion of suspected Covid-19 cases:
- New or exacerbated cough: Yes/No
- Sore throat: Yes/No
- Fever: Yes/No
- Intestinal gastritis symptoms (Diarrhea, nausea or vomiting): Yes/No
- Anosmia (loss of smell) / Ageusia (loss of taste): Yes/No
- Shortness of breath: Yes/No
- Sputum production: Yes/No
- Weakness: Yes/No
- Headache: Yes/No
- Myalgia / athralgia: Yes/No
- Nasal congestion: Yes/No
- Hemoptysis: Yes/No
- Conjunctivitis: Yes/No Comments: If yes to any of these questions: rule out an acute health condition. If no acute cause identified, consider the person as a probable case and transfer to the warm unit.
- Atypical geriatric signs
- Sudden loss of autonomy (less than 1 week)
- Sudden change in mental state (over 1 week)
- Sudden change in behavior (new behavior or cessation of behavior (less than 1 week)
- Geriatric fever (Oral or rectal temperature greater than or equal to 37.8 C or if increase of 1.1 C compared to the usual normal T)
Other comments:
………………………………………………………………………………………………………….. ........................................................................................................................................................................................................................................................................................................................................................................................................................................................
- Physical examination inspection:
- Assessment of mental state
- Attention span: attentive, not attentive
- State of consciousness: hyper-alert (or agitation), Lethargic (verbal), alert stupor (physical, comatose
- Basic settings:
Vital signs:
Pulse: ……… / min TA: .......... / ……………. T: ................ C (fever if bu oral or rectal sup or equal 37.8 C or if 1.1 C increase compared to the usual normal T)
Breathing:
Frequency: ......... / min
Type: Abdominal chest
Amplitude: normal deep surface
Rhythm: regular irregular
Draw: yes no
Saturation (normal to 94% and +, unless otherwise indicated):
Saturation: ............% ambient AIr With O2 …… ..L / min
- Auscultation:
Anterior side
Abnormal noise: Yes No
Name if possible:
Sibilant
Ronchis
Right bronchus (A)
Left bronchus (B)
Posterior side
Presence of abnormal noise:
Yes
No
Name if possible:
Sibilant
Crackling
Lower right row
Left lower lobe
- Medical decision making
Prescribed screening test (oro-nasopharyngeal sample): yes no
If the sample confirms the presence of COVID-19, isolate the patient in the warm unit.
- Clinical monitoring of COVID-19 confirmed or suspected
Stable patient
Respiratory rate : q 2h and as needed
SpO2 and Temperature: per day and as needed
Blood pressure and Cardiac frequency: per day
Unstable patient (having had an episode of respiratory distress)
Respiratory rate: every hour and as needed
SpO2 and Temperature: per day and as needed
Surname and first name of doctor
Permits
Signature
DD / MM / YYYY
HH: MM
References:
- - Liu PT, Stenger S, et al. Toll like receptor triggering of a vitamin D mediated humanantimicrobial response. Science, 2006, 311 : 1770.
- - Rapport de l'Académie nationale de médecine. Statut vitaminique, rôle extra osseux etbesoins quotidiens en vitamine D. Bull Acad Natle Med. 2012, 196, 1011.
- - Laird E, Rhodes JM and Kenny RA. Vitamin D and inflammation : potential implications for severity of Covid-19. Irish med J, 2020, 113 : 81.
- - McCartney DM, Byrne DG. Optimisation of vitamin D status impact mortality fromSARS -CoV-2 infection Irish Med J .2020 113 : 58.5- Lips P, Cashman KD, et al. Current vitamin D status in European and Middle East countries and strategies to prevent vitamin D deficiency : a position statement of the European Calcified Tissue Society. Eur J Endocrinol, 2019, 180 : P23-P54.
Links:
https://lnkd.in/eqAGhDH https://lnkd.in/epFKVEY
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 9 Months
Who may qualify
- Ages
- 15 to 75 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- * Age: 15-75 * Sex: M, F
Key inclusion criteria (3 listed)
- Fulfill Inclusion criteria and accept
- COVID-19 patients confirmed
- be regular on appointments
Key exclusion criteria (3 listed)
- COVID-19 suspected clinically
- Children
- refuse to participate
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Number of participants with treatment-TOMEKA® usage as assessed by Education
Time frame: 9 months
Change people's behaviour
1 secondary outcome
Change From Baseline in nutraceuticals usage on the care of the Covid-19 at 9 months
Time frame: 9 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Jun 2020.
- BackgroundThis phenomenon generally follows a North-South gradient, although there are exceptions such as the Nordic countries where the supplementation of the nutrients in vitamin D, in particular milk products, is systematic. On the other hand, the countries of southern Europe surprisingly display a high prevalence of vitamin D deficiency despite higher sunshine
- BackgroundThis would explain why children who receive vitamin D regularly have asymptomatic forms of Covid-19 and fewer complications. Vitamin D cannot be considered as a preventive or curative treatment for SARS-CoV-2 infection; but by mitigating the inflammatory storm and its consequences, it could be considered as an adjunct to any form of therapy.
- BackgroundThe National Academy of Medicine in France recalls that the administration of vitamin D orally is a simple, inexpensive measure and reimbursed by Health Insurance; - confirms its recommendation to ensure vitamin D supplementation in the French population in a report in 2012 [2]; - recommend that the serum vitamin D level (i.e. 25OHD) be measured quickly in people over 60 years of age with Covid-19, and that it be administered in the event of a deficiency , a loading dose of 50,000 to 100,000 IU which could help limit respiratory complications; - recommends providing vitamin D supplementation of 800 to 1,000 IU / day in people under the age of 60 as soon as the diagnosis of Covid-19 is confirmed.
- Results publicationNow is the time to give extra attention to a balanced diet and assure an optimum dietary micronutrient and vitamin intake! Particularly the micronutrient selenium plays an essential role in antioxidant functioning and helps to alleviate negative health impacts of viral infections, including inflammation of the lungs
- Results publicationParticularly elderly people are often selenium-deficient, which was proven to be the case in e.g. Italy
- Results publicationHowever, when taking micronutrient and vitamin supplements, also follow the instructions to avoid over-supplementation! A healthy and balanced diet is the safest way towards an appropriate dietary micronutrient and vitamin intake.
- Results publicationVitamin D is a prohormone synthesized in the dermis under the effect of ultraviolet rays, that is to say of the rays of the sun, then transported in the liver and the kidney where it is transformed into an active hormone. It is responsible for the intestinal absorption of calcium and bone health, but vitamin D also has unconventional effects. In particular, it modulates the functioning of the immune system by stimulating macrophages and dendritic cells.
- Results publicationIt plays a role in regulating and suppressing the cytokine inflammatory response which causes acute respiratory distress syndrome which characterizes the severe and often lethal forms of Covid-19. A significant correlation between low serum vitamin D levels and mortality by Covid-19 has been shown.
- Guillin OM, Vindry C, Ohlmann T, Chavatte L. Selenium, Selenoproteins and Viral Infection. Nutrients. 2019;11(9):2101. Published 2019 Sep 4. doi:10.3390/nu11092101Link provided by the sponsor.
- Lauretani F, Semba RD, Bandinelli S, et al. Low plasma selenium concentrations and mortality among older community-dwelling adults: the InCHIANTI Study. Aging Clin Exp Res. 2008;20(2):153-158. doi:10.1007/BF03324762Link provided by the sponsor.
- Individual participant dataSharing planned: Yes. Through researchgate website
Related trials for COVID-19
Not yet recruitingPhase 1
Phase I Open-Label Safety Trial of Pembrolizumab for Neurological Post- Acute Sequelae of SARS-CoV-2 (PD1-PASC I)
Post-Acute COVID-19 Syndrome
Active, not recruitingPhase 1
A Safety and Immunogenicity Trial of OCU500, ChAd36 Vector Encoding SARS-CoV-2 Spike Vaccine Via Intranasal and Inhalational Routes in Previously Vaccinated Adults
COVID-19
Active, not recruiting
Intervention to Address Disparate Mental Health Consequences of COVID-19 Pandemic on Latinx and African Newcomers
Mental Health Issue, Mental Health Disorder
Recruiting
Home-Based Exercise Tele-Rehabilitation After COVID-19
Post SARS-CoV2 (COVID-19)
Not yet recruitingPhase 1
A Safety, Reactogenicity and Immunogenicity Trial of RVX-sCPD9 Booster Intranasal COVID-19 Vaccine
COVID -19
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
GUYGUY KABUNDI TSHIMA, MD principal investigator
University of Kinshasa
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of COVID-19, run by University of Kinshasa at 1 site in Democratic Republic of the Congo.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 16 Jun 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Democratic Republic of the Congo. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact TSHIMA, MD (15143819264, guyguytshimakabundi@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of participants with treatment-TOMEKA® usage as assessed by Education (time frame: 9 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04424940, which also lists 8 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jun 2020.