Long CovidFASTCOV-PNCT06522750
Periodic Fasting for Treatment of Long Covid in Adults: a Pilot Study
A study testing 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method in people with Long Covid and Chronic Inflammation, run by University of Luxembourg at 1 site in Luxembourg.
Trial summary
Background: Long COVID, characterized by persistent symptoms following acute COVID-19 infection, has emerged as a significant public health concern. Symptoms range from fatigue, cognitive impairments, to respiratory difficulties, affecting patients\' quality of life. Read more about this study
- Who is it for?
- Ages 18 to 64 years
- Conditions the study is for
- Long Covid, Chronic Inflammation
- What is being tested?
- 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteLuxembourg
- Study dates
- 19 Feb 2025to 30 Sep 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 18 to 64 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Age 18-64
- Diagnosis Long Covid Syndrome (post-acute COVID-19 symptoms persisting ≥12 weeks)
- Normal body Mass Index (18.5 to 25 kg/m2)
- Marginal Iron status ( PF< 25 ng/ml)
- Able to communicate in and comprehend English and/or German and/or French language
- Present written / signed declaration of consent
- Ability to understand the patient information and willingness to sign the consent form
- Consent to specimen collection and specimen use
Who cannot join
- Current underweight condition (body mass index less than 18.5 kg/m2) or weight loss exceeding 3 kg within the last month or 5 kg within the last three months.
- Existing / current eating disorder within the past five years (e.g., anorexia, bulimia).
- Psychiatric condition that limits understanding of the examination protocol (unable to consent)
- Severe internal disease (e.g. kidney deficiency with creatinine > 2mg/dl), chronic inflammatory illness other than LCS
- Participation in another intervention study.
- Existing vegan diet or fasting during the last six months
Show all 13Show fewer
- Pregnancy or breastfeeding status.
- Presence or suspicion of pre-existing ME/CFS or early autonomous dysfunction
- Diagnosis of chronic inflammatory bowel diseases, celiac disease or colorectal cancer according to the guidelines of the German Society of Gastroenterology
- Use of anti-psychotic drugs
- Antibiotic use during the previous 12 months
- Start of novel drug therapy
- Contraindication for additional blood draws (e.g. hemoglobin <10)
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Luxembourg1 site, 1 recruiting
- Recruiting
Rehaklinik CHNP
Ettelbruck, L-9012
Raquel Gómez-Bravo Gómez-Bravo, MD PhD, raquel.gomezbravo@chnp.lu
About this study
Official title: Pilot Study on the Feasibility of an RCT: Evaluating Periodic Fasting as a Treatment Strategy for Long Covid in Adults
Background:
Long COVID, characterized by persistent symptoms following acute COVID-19 infection, has emerged as a significant public health concern. Symptoms range from fatigue, cognitive impairments, to respiratory difficulties, affecting patients\' quality of life. Dietary interventions, particularly fasting, have historically been used to modulate immune responses and improve health outcomes in various conditions. The Buchinger-Wilhelmi method represents a structured and medically supervised fasting approach. Given the inflammatory nature of long COVID, fasting may offer therapeutic benefits by modulating the immune response, enhancing cellular repair mechanisms, and resetting metabolic processes.
Read more
Objectives:
This clinical trial aims to assess the feasibility of a 7-day ambulatory fasting intervention using the Buchinger-Wilhelmi method on long COVID patients as primary objective. As secondary objectives, the study will investigate the potential beneficial impact of fasting on clinical, biological, and psychological parameters over a period of 4 weeks, offering insights into potential therapeutic avenues for long COVID management.
Study timeline:
The research will span a period of 4 weeks
Study population:
This study aims to recruit around 20 participants, who will all receive a fasting intervention using the Buchinger-Wilhelmi method.
Biological sample and data collection:
Participants will undergo various data and sample collection procedures, including blood draws of up to 90 42 ml per visit, collection of peripheral mononuclear cells, stool samples, and completion of questionnaires in a smartphone-based Application (MyCap).
Sample analysis:
The collected samples will be subjected to a range of analyses, including the assessment of serological markers for routine blood chemistry, evaluation of inflammation markers, and examination of stool samples.
Read the detailed description
Background Long COVID syndrome (LCS) is a heterogeneous clinical condition that develops after acute SARS-CoV-2 infection, affecting at least 10% of patients. LCS is characterized by persistent symptoms lasting longer than 2-3 months following a confirmed SARS-CoV-2 infection. The most disruptive symptoms include fatigue, shortness of breath, pain, depression/anxiety, and cognitive impairment, significantly impacting daily activities, income, and quality of life.
Pathophysiology of LCS
Immunological Dysregulation:
Persistent activation of monocyte populations, including resident and infiltrating macrophages, dendritic cells, and neutrophils, potentially causing tissue damage.
Reservoirs of SARS-CoV-2 may persist, particularly in respiratory and gastrointestinal tracts, contributing to ongoing lymphocyte activation.
Autoimmunity involving T-cells and B-cells has been observed, with cytokines such as interferon gamma, IL-2, IL-4, IL-6, IL-8, IL-10, and IL-17 frequently implicated.
Tissue fibrosis, a consequence of inflammation, is commonly reported.
Vascular Dysfunction and Coagulopathy:
Impaired fibrinolysis and platelet hyperactivation contribute to microclot formation, entrapping pro-inflammatory molecules like IL-6.
Platelet-poor plasma in LCS patients shows high levels of fibrin amyloid microclots, impairing microcirculation and exacerbating immunopathology.
Aberrant immune cell activity increases thrombosis through autoantibodies and NETosis.
Persistent endothelial dysfunction is a common feature, contributing to numerous LCS symptoms.
Gastrointestinal Involvement:
SARS-CoV-2 infection reduces intestinal microbiota diversity, with recovery correlating to reduced LCS risk.
Specific bacterial taxa, such as Escherichia, are associated with severe COVID-19 and LCS.
Functional dyspepsia and irritable bowel syndrome, related to microbial dysbiosis, are common post-COVID conditions.
Gut microbiota influences LCS-related biological functions, particularly psychological symptoms, through modulation of brain chemicals and gut-blood barrier disruption.
Potential of Fasting as a Treatment for LCS Fasting shows promise as a treatment for LCS by modulating the same cellular systems affected by LCS. A recent small study indicated that 92% of LCS patients experienced symptom improvement during long-term fasting, with notable effects on circulating inflammatory molecules, C-reactive protein levels, and dyslipidemia. Fasting can increase beneficial gut microbial genera and alter blood metabolites, potentially disrupting dysfunctional circuits in LCS.
Significance LCS affects over 150 million people worldwide, with more than half experiencing significant work and lifestyle disruptions. Effective, low-cost, and attainable therapeutic options are urgently needed. Medically supervised fasting, particularly intermittent fasting, could be an accessible and safe intervention with minimal physician oversight and low malnutrition risk. Fasting may also prevent other chronic illnesses associated with LCS, such as type 2 diabetes mellitus.
Hypothesis Our primary hypothesis is that ambulatory fasting intervention using the Buchinger-Wilhelmi method is a feasible treatment for LCS. We propose that medically supervised long-term fasting will improve perceived health and quality of life in LCS patients by disrupting inflammatory immuno-metabolic feed-forward loops, thus ameliorating immune and vascular pathologies.
Methodology and Analysis Patient Eligibility
Inclusion Criteria:
Age 18-64 Diagnosis of LCS (post-acute COVID-19 symptoms persisting ≥12 weeks) Normal BMI (18.5 to 25 kg/m²) Marginal iron status (PF < 25 ng/ml) Ability to communicate in and comprehend English, German, or French Written and signed consent Willingness to consent to specimen collection and use
Exclusion Criteria:
BMI < 18.5 kg/m² or significant recent weight loss History of eating disorders within the past five years Severe internal disease or chronic inflammatory illness other than LCS Participation in another intervention study Recent fasting or vegan diet Pregnancy or breastfeeding Existing ME/CFS or early autonomous dysfunction Chronic inflammatory bowel diseases, celiac disease, or colorectal cancer Use of anti-psychotic drugs or recent antibiotic use Contraindication for additional blood draws Start of novel drug therapy Intervention
The primary goal is to perform a single period of periodic fasting (PF) using the Buchinger procedure, involving an initial bowel cleanse followed by a 7-day fasting period. The fasting regimen includes:
Preparation Phase: Three days of relief with reduced food intake, avoiding stimulants.
Fasting Week: A laxative fluid intake on the first day, followed by 7 days of a dietary energy supply of a maximum of 350 kcal per day (vegetable broths and juices), and consumption of calorie-free water or tea.
Support and Guidance: Detailed instructions, face-to-face consultations, and digital application (MyCap) for adherence confirmation via urine ketone measurements.
Sample and Data Collection Sample Size: 20 patients for the pilot study to test feasibility.
Study Outline:
Inclusion visit for risk explanation, medical history, and physical examination.
Daily follow-up via telephone and online appointments during the fasting phase. Questionnaire-based assessment via MyCap Smartphone Application.
Parameters to be Quantified:
Blood samples for safety parameters, metabolites, immune activity indicators, and additional analyses.
Stool samples for microbiome composition and activity. Urine samples for metabolomics. Saliva samples for cortisol measurements. Analysis and Results Interpretation Results will be analyzed descriptively, with means, standard deviations, and graphs summarizing data. Exploratory analysis will identify patterns, trends, or unexpected results. Correlation with improvement in biomedical parameters will be assessed, with a larger study needed for establishing causal links.
Risks Blood Draw: Discomfort, bleeding, swelling, pain, rare nerve damage, or infection at the injection site, and fainting risk.
Periodic Fasting Protocol: Reduction in blood pressure, closely monitored with non-medical interventions if necessary.
Data Collection and Storage Data is collected using REDCap, a secure, web-based software platform, with pseudonymized data stored for at least 10 years post-study. The Principal Investigator ensures compliance with national laws and GDPR.
Regulatory and Ethical Considerations Informed Consent: Participants receive an easily understood Participant Information Sheet and Informed Consent Form, with contact information for study personnel.
Confidentiality and Privacy: Compliance with national laws and GDPR, with pseudonymized data transfer to third parties only with participant consent.
Financing and Insurance: Supported by the Direction de la Santé, CHNP, and the University of Luxembourg.
Conclusion This pilot study aims to test the feasibility of using the Buchinger-Wilhelmi fasting method for treating LCS. If successful, fasting could provide a low-cost, accessible, and effective therapeutic option for LCS sufferers worldwide.
- Conditions
- Long Covid, Chronic Inflammation
- Being tested
- 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method
- Keywords
- long covid, fasting, caloric restriction, chronic inflammation, dysbiosis, mitochondrial dysfunction, thrombosis
- Medical subject headings
- Post-Acute COVID-19 Syndrome, Fasting, Dysbiosis, Mitochondrial Diseases, Thrombosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi methodOther
Buchinger-Wilhelmi method, will be administered in an ambulatory setting under physician guidance. It involves an initial bowel cleanse followed by 7-day fasting period. The initial bowel cleanse will be performed according to the standard procedure commonly used for colonoscopy preparation. During the fasting period, subjects will be provided with a dietary energy supply of a maximum of 350 kcal per day, primarily consisting of vegetable broths as well as fresh vegetable juices. Patients will only be allowed to consume calorie-free and unsweetened water or tea in addition to the prescribed diet.
| Study group | Role | What they receive |
|---|---|---|
| 20 participants. Long covid patients. | Experimental | All patients will undergo a caloric restriction diet for a week.This begins with the intake of a laxative fluid on the first fasting day. This fluid aids in bowel emptying, akin to preparations for a colonoscopy. Detailed instructions on how to use it will be provided along with the laxative, and the study physician or dietary team will discuss dosage and intake with you. The caloric restriction period will last for 7 days and then be broken with the consumption of an apple. Following the breaking of the fast, three build-up days will follow to gradually increase food intake. Receives: Other: 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method |
What is being measured
The primary outcome is the main question the study is designed to answer.
Nutritional protocol
Patient's level of health and wellbeing from a nutritional point of view
Measured: 4 weeks
Fatigue assessment Scale (FAS)
Level of fatigue through three factors (General Fatigue, Physical Fatigue and Concentration/Motivation).
Measured: 4 weeks
Quality of Life (WHOQOL)
Quality of Life as an individual's perception of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards and concerns.
Measured: 4 weeks
Functionality (WHODAS 2.0)
Impact of Long Covid in terms of functioning.
Measured: 4 weeks
Anxiety (GAD-7)
Generalized anxiety disorder in the last 2 weeks
Measured: 4 weeks
Depression (PHQ-9)
Presence and severity of depressive symptoms
Measured: 4 weeks
Mood States
Transient fluctuating moods or affective states
Measured: 4 weeks
Blood preasure
Force or pressure of blood on the arteries when the heart is pumping
Measured: 4 weeks
Secondary outcomes (7)
Urine Metabolomics
Metabolites in urine
Measured: 4 weeks
Gut Microbiome
Microbiota in stool
Measured: 4 weeks
Stool Metabolomics
Metabolites in stool
Measured: 4 weeks
Blood cytokines
Cytokines using Quanterix technology
Measured: 4 weeks
Blood Mitochondrial dysfunction
Mitochondrial cell-free DNA
Measured: 4 weeks
Blood Epigenetics
Methylation profiling microarray
Measured: 4 weeks
Blood test
Metabolites in blood
Measured: 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jul 2024
- Study start19 Feb 2025
- Primary completion30 Jun 2025 (estimated)
- Study completion30 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Long CovidStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Luxembourg
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Raquel Gomez Bravo, PhD, Principal investigator, Rehaklinik du Centre Hospitalier Neuro-Psychiatrique (CHNP), UL
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06522750
- Sponsor's protocol ID
- 202401/03
- Acronym
- FASTCOV-P
- Status last verified
- Mar 2025
- First submitted
- 17 May 2024
- Last updated
- 30 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pilot Study on the Feasibility of an RCT: Evaluating Periodic Fasting as a Treatment Strategy for Long Covid in Adults
- ClinicalTrials.gov ID
- NCT06522750
- Acronym / sponsor ID
- FASTCOV-P / 202401/03
- Conditions
- Long Covid, Chronic Inflammation
- Keywords
- long covid, fasting, caloric restriction, chronic inflammation, dysbiosis, mitochondrial dysfunction, thrombosis
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- University of LuxembourgUniversity, hospital or other
- Study start
- 19 Feb 2025 (actual)
- Primary completion
- 30 Jun 2025 (estimated)
- Study completion
- 30 Sep 2025 (estimated)
- First posted
- 26 Jul 2024 (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.
Background:
Long COVID, characterized by persistent symptoms following acute COVID-19 infection, has emerged as a significant public health concern. Symptoms range from fatigue, cognitive impairments, to respiratory difficulties, affecting patients\' quality of life. Dietary interventions, particularly fasting, have historically been used to modulate immune responses and improve health outcomes in various conditions. The Buchinger-Wilhelmi method represents a structured and medically supervised fasting approach. Given the inflammatory nature of long COVID, fasting may offer therapeutic benefits by modulating the immune response, enhancing cellular repair mechanisms, and resetting metabolic processes.
Objectives:
This clinical trial aims to assess the feasibility of a 7-day ambulatory fasting intervention using the Buchinger-Wilhelmi method on long COVID patients as primary objective. As secondary objectives, the study will investigate the potential beneficial impact of fasting on clinical, biological, and psychological parameters over a period of 4 weeks, offering insights into potential therapeutic avenues for long COVID management.
Study timeline:
The research will span a period of 4 weeks
Study population:
This study aims to recruit around 20 participants, who will all receive a fasting intervention using the Buchinger-Wilhelmi method.
Biological sample and data collection:
Participants will undergo various data and sample collection procedures, including blood draws of up to 90 42 ml per visit, collection of peripheral mononuclear cells, stool samples, and completion of questionnaires in a smartphone-based Application (MyCap).
Sample analysis:
The collected samples will be subjected to a range of analyses, including the assessment of serological markers for routine blood chemistry, evaluation of inflammation markers, and examination of stool samples.
Detailed description
Background Long COVID syndrome (LCS) is a heterogeneous clinical condition that develops after acute SARS-CoV-2 infection, affecting at least 10% of patients. LCS is characterized by persistent symptoms lasting longer than 2-3 months following a confirmed SARS-CoV-2 infection. The most disruptive symptoms include fatigue, shortness of breath, pain, depression/anxiety, and cognitive impairment, significantly impacting daily activities, income, and quality of life.
Pathophysiology of LCS
Immunological Dysregulation:
Persistent activation of monocyte populations, including resident and infiltrating macrophages, dendritic cells, and neutrophils, potentially causing tissue damage.
Reservoirs of SARS-CoV-2 may persist, particularly in respiratory and gastrointestinal tracts, contributing to ongoing lymphocyte activation.
Autoimmunity involving T-cells and B-cells has been observed, with cytokines such as interferon gamma, IL-2, IL-4, IL-6, IL-8, IL-10, and IL-17 frequently implicated.
Tissue fibrosis, a consequence of inflammation, is commonly reported.
Vascular Dysfunction and Coagulopathy:
Impaired fibrinolysis and platelet hyperactivation contribute to microclot formation, entrapping pro-inflammatory molecules like IL-6.
Platelet-poor plasma in LCS patients shows high levels of fibrin amyloid microclots, impairing microcirculation and exacerbating immunopathology.
Aberrant immune cell activity increases thrombosis through autoantibodies and NETosis.
Persistent endothelial dysfunction is a common feature, contributing to numerous LCS symptoms.
Gastrointestinal Involvement:
SARS-CoV-2 infection reduces intestinal microbiota diversity, with recovery correlating to reduced LCS risk.
Specific bacterial taxa, such as Escherichia, are associated with severe COVID-19 and LCS.
Functional dyspepsia and irritable bowel syndrome, related to microbial dysbiosis, are common post-COVID conditions.
Gut microbiota influences LCS-related biological functions, particularly psychological symptoms, through modulation of brain chemicals and gut-blood barrier disruption.
Potential of Fasting as a Treatment for LCS Fasting shows promise as a treatment for LCS by modulating the same cellular systems affected by LCS. A recent small study indicated that 92% of LCS patients experienced symptom improvement during long-term fasting, with notable effects on circulating inflammatory molecules, C-reactive protein levels, and dyslipidemia. Fasting can increase beneficial gut microbial genera and alter blood metabolites, potentially disrupting dysfunctional circuits in LCS.
Significance LCS affects over 150 million people worldwide, with more than half experiencing significant work and lifestyle disruptions. Effective, low-cost, and attainable therapeutic options are urgently needed. Medically supervised fasting, particularly intermittent fasting, could be an accessible and safe intervention with minimal physician oversight and low malnutrition risk. Fasting may also prevent other chronic illnesses associated with LCS, such as type 2 diabetes mellitus.
Hypothesis Our primary hypothesis is that ambulatory fasting intervention using the Buchinger-Wilhelmi method is a feasible treatment for LCS. We propose that medically supervised long-term fasting will improve perceived health and quality of life in LCS patients by disrupting inflammatory immuno-metabolic feed-forward loops, thus ameliorating immune and vascular pathologies.
Methodology and Analysis Patient Eligibility
Inclusion Criteria:
Age 18-64 Diagnosis of LCS (post-acute COVID-19 symptoms persisting ≥12 weeks) Normal BMI (18.5 to 25 kg/m²) Marginal iron status (PF < 25 ng/ml) Ability to communicate in and comprehend English, German, or French Written and signed consent Willingness to consent to specimen collection and use
Exclusion Criteria:
BMI < 18.5 kg/m² or significant recent weight loss History of eating disorders within the past five years Severe internal disease or chronic inflammatory illness other than LCS Participation in another intervention study Recent fasting or vegan diet Pregnancy or breastfeeding Existing ME/CFS or early autonomous dysfunction Chronic inflammatory bowel diseases, celiac disease, or colorectal cancer Use of anti-psychotic drugs or recent antibiotic use Contraindication for additional blood draws Start of novel drug therapy Intervention
The primary goal is to perform a single period of periodic fasting (PF) using the Buchinger procedure, involving an initial bowel cleanse followed by a 7-day fasting period. The fasting regimen includes:
Preparation Phase: Three days of relief with reduced food intake, avoiding stimulants.
Fasting Week: A laxative fluid intake on the first day, followed by 7 days of a dietary energy supply of a maximum of 350 kcal per day (vegetable broths and juices), and consumption of calorie-free water or tea.
Support and Guidance: Detailed instructions, face-to-face consultations, and digital application (MyCap) for adherence confirmation via urine ketone measurements.
Sample and Data Collection Sample Size: 20 patients for the pilot study to test feasibility.
Study Outline:
Inclusion visit for risk explanation, medical history, and physical examination.
Daily follow-up via telephone and online appointments during the fasting phase. Questionnaire-based assessment via MyCap Smartphone Application.
Parameters to be Quantified:
Blood samples for safety parameters, metabolites, immune activity indicators, and additional analyses.
Stool samples for microbiome composition and activity. Urine samples for metabolomics. Saliva samples for cortisol measurements. Analysis and Results Interpretation Results will be analyzed descriptively, with means, standard deviations, and graphs summarizing data. Exploratory analysis will identify patterns, trends, or unexpected results. Correlation with improvement in biomedical parameters will be assessed, with a larger study needed for establishing causal links.
Risks Blood Draw: Discomfort, bleeding, swelling, pain, rare nerve damage, or infection at the injection site, and fainting risk.
Periodic Fasting Protocol: Reduction in blood pressure, closely monitored with non-medical interventions if necessary.
Data Collection and Storage Data is collected using REDCap, a secure, web-based software platform, with pseudonymized data stored for at least 10 years post-study. The Principal Investigator ensures compliance with national laws and GDPR.
Regulatory and Ethical Considerations Informed Consent: Participants receive an easily understood Participant Information Sheet and Informed Consent Form, with contact information for study personnel.
Confidentiality and Privacy: Compliance with national laws and GDPR, with pseudonymized data transfer to third parties only with participant consent.
Financing and Insurance: Supported by the Direction de la Santé, CHNP, and the University of Luxembourg.
Conclusion This pilot study aims to test the feasibility of using the Buchinger-Wilhelmi fasting method for treating LCS. If successful, fasting could provide a low-cost, accessible, and effective therapeutic option for LCS sufferers worldwide.
Study design
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 20 participants. Long covid patients. | Experimental | Other: 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi methodAll patients will undergo a caloric restriction diet for a week.This begins with the intake of a laxative fluid on the first fasting day. This fluid aids in bowel emptying, akin to preparations for a colonoscopy. Detailed instructions on how to use it will be provided along with the laxative, and the study physician or dietary team will discuss dosage and intake with you. The caloric restriction period will last for 7 days and then be broken with the consumption of an apple. Following the breaking of the fast, three build-up days will follow to gradually increase food intake. |
Who may qualify
- Ages
- 18 to 64 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (8 listed)
- Age 18-64
- Diagnosis Long Covid Syndrome (post-acute COVID-19 symptoms persisting ≥12 weeks)
- Normal body Mass Index (18.5 to 25 kg/m2)
- Marginal Iron status ( PF< 25 ng/ml)
- Able to communicate in and comprehend English and/or German and/or French language
Key exclusion criteria (13 listed)
- Current underweight condition (body mass index less than 18.5 kg/m2) or weight loss exceeding 3 kg within the last month or 5 kg within the last three months.
- Existing / current eating disorder within the past five years (e.g., anorexia, bulimia).
- Psychiatric condition that limits understanding of the examination protocol (unable to consent)
- Severe internal disease (e.g. kidney deficiency with creatinine > 2mg/dl), chronic inflammatory illness other than LCS
- Participation in another intervention study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi methodBuchinger-Wilhelmi method, will be administered in an ambulatory setting under physician guidance. It involves an initial bowel cleanse followed by 7-day fasting period. The initial bowel cleanse will be performed according to the standard procedure commonly used for colonoscopy preparation. During the fasting period, subjects will be provided with a dietary energy supply of a maximum of 350 kcal per day, primarily consisting of vegetable broths as well as fresh vegetable juices. Patients will only be allowed to consume calorie-free and unsweetened water or tea in addition to the prescribed diet. | Other | 20 participants. Long covid patients. |
Primary outcome
Nutritional protocol
Time frame: 4 weeks
Patient's level of health and wellbeing from a nutritional point of view
Fatigue assessment Scale (FAS)
Time frame: 4 weeks
Level of fatigue through three factors (General Fatigue, Physical Fatigue and Concentration/Motivation).
Quality of Life (WHOQOL)
Time frame: 4 weeks
Quality of Life as an individual's perception of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards and concerns.
Functionality (WHODAS 2.0)
Time frame: 4 weeks
Impact of Long Covid in terms of functioning.
Anxiety (GAD-7)
Time frame: 4 weeks
Generalized anxiety disorder in the last 2 weeks
Depression (PHQ-9)
Time frame: 4 weeks
Presence and severity of depressive symptoms
Mood States
Time frame: 4 weeks
Transient fluctuating moods or affective states
Blood preasure
Time frame: 4 weeks
Force or pressure of blood on the arteries when the heart is pumping
7 secondary outcomes
Urine Metabolomics
Time frame: 4 weeks
Gut Microbiome
Time frame: 4 weeks
Stool Metabolomics
Time frame: 4 weeks
Blood cytokines
Time frame: 4 weeks
Blood Mitochondrial dysfunction
Time frame: 4 weeks
Blood Epigenetics
Time frame: 4 weeks
Blood test
Time frame: 4 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Mar 2025.
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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.
Raquel Gomez Bravo, PhD principal investigator
Rehaklinik du Centre Hospitalier Neuro-Psychiatrique (CHNP), UL
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method in people with Long Covid and Chronic Inflammation, run by University of Luxembourg at 1 site in Luxembourg.
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 8 inclusion and 13 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: looking for participants now, as of the sponsor's last update on 30 Mar 2025. 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 Luxembourg. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Marta Sanchez, PhD (+3524666446555, marta.sanchez@uni.lu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Nutritional protocol (time frame: 4 weeks). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 30 Mar 2025.