Infective EndocarditisENDOCARENCT06563609
Combined Rehabilitation and Nutritional Support vs. Standard Care in In-Hospital Endocarditis Treatment
A study testing Intensive physical Therapy, Probiotic treatment and Individualised Nutritional Support in people with Infective Endocarditis and Endocarditis, Bacterial, run by Johannes Grand at 1 site in Denmark.
Trial summary
Infective endocarditis (IE) is associated with high morbidity and mortality. Patients with IE are affected by a lengthy hospitalization, leading to physical deconditioning and a rapid decline in physical fitness, muscle mass and strength. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Infective Endocarditis, Endocarditis, Bacterial, Infection; Heart
- What is being tested?
- Intensive physical Therapy, Probiotic treatment and Individualised Nutritional Support
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 15 participants
- Where
- 1 siteDenmark
- Study dates
- 19 Feb 2025to 7 Dec 2025
- Phase
- Interventional
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Clinical diagnosis of left-sided (native, prosthetic, or culture-negative) bacterial infective endocarditis mandating iv antibiotic treatment, including Cardiac Implantable Electronic Devices infections, irrespective of cause and location as defined by the ESC modified Duke Criteria
- Age ≥ 18 years
Who cannot join
- Hemodynamic instability (defined as a systolic blood pressure <90 mmHg and lactate >2.2 mmol/l measured in an arterial blood gas.
- Expected to be discharged within 3 days
- Immunocompromised due to severe combined immunodeficiency, HIV, or hematological malignancy
- Fungal endocarditis
- Pregnancy
- Unwilling or unable to sign or understand informed consent
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Combined Physical Rehabilitation and Individualized Nutritional Support Versus Standard of Care During In-hospital Endocarditis Treatment
Infective endocarditis (IE) is associated with high morbidity and mortality. Patients with IE are affected by a lengthy hospitalization, leading to physical deconditioning and a rapid decline in physical fitness, muscle mass and strength. Moreover, prolonged antibiotic regimens frequently result in nausea, antibiotic-associated diarrhea and Clostridioides difficile (C.difficile) intestinal infections that further negatively affect patient health. These physical challenges are further exacerbated by the negative impact on mental health, increasing the overall burden of the illness. Implementing a targeted rehabilitative strategy in the hospital setting may therefore improve patient care including physical health and overall quality of life during hospitalization.
Read the detailed description
BACKGROUND:
Infective endocarditis (IE) is a severe infection of the heart's inner lining, typically the valves, carrying high risks of acute heart failure and death. Patients often face extended hospitalizations (up to six weeks or longer) for intravenous antibiotic treatments, with 30-50% requiring urgent valve surgery. The incidence of IE is 8-10 per 100,000 person-years and rising due to aging populations and increased use of cardiac implantable devices, accounting for 650-700 cases annually in Denmark. Without treatment, mortality is nearly 100%, and with treatment, it ranges from 5-30% during the initial hospitalization, influenced by factors such as infection site, causative agent, age, and comorbidities.
IE significantly impacts patients' health due to prolonged hospitalization. Many experience rapid physical decline, including reduced cardiorespiratory fitness, strength, and overall fitness, caused by bed rest, malnutrition, and limited activity. Recovery is often difficult, with worsening physical, mental, and emotional states. The POET trial found poor self-rated health triples mortality risk. Up to 35% of patients do not return to work, and 65% face readmission within a year. Long hospital stays also increase the need for nursing home care.
Malnutrition is common in IE patients, raising risks of death, illness, and impairment. Acute illness amplifies nutritional deficits, worsening muscle wasting and overall health. The EFFORT trial showed early nutritional support reduces mortality and complications, yet no randomized studies have addressed nutrition in IE patients.
Intravenous antibiotics add distress, often causing nausea, diarrhea, and C. difficile infections. Probiotics like S. boulardii show promise in preventing these side effects.
Cardiac rehabilitation has proven benefits for other heart conditions, improving exercise capacity, quality of life, and reducing readmissions. However, evidence is limited for in-hospital IE rehabilitation. Tailored, supervised programs during hospitalization could address physical and mental health needs, improving overall recovery and quality of life.
PRIMARY AIM:
To investigate the effectiveness of individualized physical rehabilitation and nutritional support designed to reduce physical deconditioning and prevent treatment-related harms thus ultimately improving mental health in patients hospitalized with endocarditis.
HYPOTHESES:
Within a 2-by-2 factorial design, a patient-centered, individualized, and adaptable physical rehabilitation and nutritional plan during lengthy hospitalization will improve mental health more than standard care.
Furthermore, in the same factorial framework, a probiotic supplement during antibiotic-treatment will decrease the rate of antibiotic-associated diarrhea compared to no probiotic supplement.
NUTRITIONAL SUPPORT:
In the intervention group, nutritional screening and support begin within 24 hours of randomization. Individualized nutritional plans are developed based on the NRS 2002 protocol and 2018 international guidelines. A dietitian sets energy requirements using the weight-adjusted Harris-Benedict equation and establishes protein intake targets between 1.2-1.5 g/kg of body weight, adjusting to 0.8 g/kg for patients with acute renal failure.
Patients are screened for risk of refeeding syndrome with routine blood tests, including magnesium, phosphate, and other relevant biomarkers (e.g., bilirubin, creatinine, albumin, electrolytes, etc.). The initial dietary plan includes hospital-provided meals, snacks from an "à la carte" menu, and oral nutritional supplements (ONS). Daily food records monitor intake, and if patients fail to meet 75% of caloric and protein targets for three consecutive days-or earlier based on clinical judgment-escalation to enteral tube feeding or parenteral feeding is initiated.
INDIVIDUALLY PLANNED PHYSICAL EXERCISE BY AN INTERDISCIPLINARY TEAM LEAD BY A SPECIALIZED REHABILITATION PHYSIOTHERAPIST:
The ENDOCARE team, consisting of a cardiologist, nurse, and physiotherapist, optionally involving a family member, will meet with the patient the first weekday after inclusion to design a personalized exercise regimen. This regimen accounts for comorbidities, performance status, disease severity, and support resources. Weekly meetings with the team will address patient concerns and ensure optimal care.
Exercise Modalities
Patients will participate in Intensive Exercise to reduce deconditioning and enhance well-being, focusing on:
Progressive Resistance Exercise: Major muscle groups (e.g., leg presses, arm rows, arm pushes) are targeted with 2-3 sessions/week, using stationary equipment or elastic bands. Training follows a linear progression (3 sets per exercise starting at 15 ± 2 RM, progressing to 10 ± 2 RM) and integrates principles like range of motion and time under tension.
Cardiovascular Exercise: Sessions involve 20 minutes of moderate-intensity exercise (Borg RPE 12-14) 3-4 times/week, using arm ergometers or stationary beds. Intensity and structure (continuous or interval) are adjusted based on patient preference.
Physical Activity Daily physical activity, guided by Danish recommendations (10,000 steps/day), is encouraged using a gradual progression model (e.g., PACE-UP). Activity monitoring is supported by SENS motion accelerometers, with data transferred to a smartphone app. Depending on funding, tablets may provide real-time feedback on activity levels near patient beds.
Control Group Patients in the control group receive standard hospital care, including an initial physiotherapist assessment and 1-2 supervised or self-managed exercise sessions per week.
Risks Potential risks include musculoskeletal injuries (e.g., strains, sprains), fatigue, and overtraining.
GUIDE FOR PROBIOTIC ADMINISTRATION:
In the intervention group, S. boulardii treatment begins at inclusion. Patients will receive Sacchaflor capsules (Pharmaforce Aps), containing S. boulardii (5×10^9 DBVPG 6763 strain) and mannan oligosaccharide (MOS), a supplement derived from Saccharomyces cerevisiae. The capsules are administered twice daily until the end of antibiotic treatment. If the patient is discharged with continued antibiotics, S. boulardii will be used for up to 30 more days.
In the control group, no probiotics will be given for 30 days post inclusion.
Possible side effects include gastrointestinal disturbances (e.g., flatulence, bloating, constipation) and, rarely, fungemia or allergic reactions).
- Conditions
- Infective Endocarditis, Endocarditis, Bacterial, Infection; Heart, Bacteremia, Cardiac Rehabilitation, Nutrition Intervention
- Being tested
- Intensive physical Therapy, Probiotic treatment, Individualised Nutritional Support, Standard hospital care
- Keywords
- Infective endocarditis, Endocarditis team, Physical Therapy, Individualized Nutritional Support, Probiotic yeast Saccharomyces Boulardii, Cardiac rehabilitation
- Medical subject headings
- Endocarditis, Endocarditis, Bacterial, Infections, Bacteremia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Intensive physical TherapyBehavioural
Tailored exercise programs supervised by trained physiotherapists, focusing on improving cardiorespiratory fitness, strength, and functional capacity.
Probiotic treatmentDietary supplement
Administration of probiotic yeast Saccharomyces boulardii twice daily
Individualised Nutritional SupportBehavioural
Personalized nutritional plans guided by a dietitian, addressing malnutrition and caloric/protein deficiencies with daily caloric intake adjustments and supplements if necessary based on the EFFORT trial.
Standard hospital careOther
Patients will receive standard hospital care
| Study group | Role | What they receive |
|---|---|---|
| Integrated Physical Therapy and Nutritional Support with Probiotic Saccharomyces boulardii | Active comparator | Intensive physical therapy + individualised nutritional support + administration of probiotic yeast saccharomyces boulardii Receives: Behavioral: Intensive physical Therapy; Dietary Supplement: Probiotic treatment; Behavioral: Individualised Nutritional Support |
| A combined Intensive physical Therapy and individualised Nutritional Support intervention | Active comparator | Intensive physical Therapy + Individualised Nutritional Support Receives: Behavioral: Intensive physical Therapy; Behavioral: Individualised Nutritional Support |
| Administration of probiotic yeast Saccharomyces boulardii | Active comparator | Administration of probiotic yeast Saccharomyces boulardii Receives: Dietary Supplement: Probiotic treatment |
| Control group | Placebo comparator | Standard hospital care Receives: Other: Standard hospital care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mental health (MH) measured by the standardized Short Form 36 (SF-36)
Mental Component Summary (MCS) of the Medical Outcome Study Short Form 36 version 2 (SF-36) which has been validated in Danish and in cardiac populations and is widely used in controlled clinical trials. Scores range from 0 to 100, with higher scores indicating better-perceived health
Measured: 30 days
Secondary outcomes (5)
Change in number of sit and stand in 30 seconds from baseline to 14 days
Sit and stand test
Measured: 14 days
Quality of life from EQ-5D
Quality of life measured efte 30 days using EuroQol-5 Domain (EQ-5D) The EQ VAS records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'. The VAS can be used as a quantitative measure of health outcome that reflect the patient's own judgement.
Measured: 14, 30, and 90 days follow-up
Days alive without diarrhea
Assessment with Bristol Stool Chart
Measured: 30 days in hospital and 90 days out of hospital
Days alive and out of hospital
Measured: 30 day in hospital, and 90 day out-of-hospital
All-cause mortality
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Aug 2024
- Study start19 Feb 2025
- Primary completion7 Dec 2025
- Study completion7 Dec 2025
Why it stopped: Slow recruitment
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Infective EndocarditisStudies 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Investigator-initiated, randomized, single-center, 2-by-2 factorial clinical trial with co-enrolment into two different non-pharmacological interventions. * A combined Intensive physical Therapy and individualised Nutritional Support intervention and administration of probiotic yeast Saccharomyces boulardii * A combined Intensive physical Therapy and individualised Nutritional Support intervention and NO administration of probiotic yeast Saccharomyces boulardii * Administration of probiotic yeast Saccharomyces boulardii and NO Intensive physical Therapy and individualised Nutritional Support. * NO administration of probiotic yeast Saccharomyces boulardii and NO Intensive physical Therapy and individualised Nutritional Support. Patients will receive standard hospital care
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 15 participants (actual)
Sponsor and investigators
- Lead sponsor
- Johannes Grand
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Johannes Grand, Copenhagen University Hospital, Hvidovre
- Investigators
- Johannes Grand, MD, PhD, Principal investigator, Copenhagen University Hospital Amager-Hvidovre, Department of Cardiology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06563609
- Sponsor's protocol ID
- ENDOCARE-001
- Acronym
- ENDOCARE
- Status last verified
- Dec 2025
- First submitted
- 19 Aug 2024
- Last updated
- 15 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Individual participant data that underlie the results reported in the publication will be shared. Data will be available beginning after publicatoin of the main papers. Access will be granted to researchers who provide a methodologically sound proposal, which will be reviewed by the national governing body for approval both regarding ethics and patients data safety.
Study at a glance
From the registry record, last updated by the sponsor on 15 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Combined Physical Rehabilitation and Individualized Nutritional Support Versus Standard of Care During In-hospital Endocarditis Treatment
- ClinicalTrials.gov ID
- NCT06563609
- Acronym / sponsor ID
- ENDOCARE / ENDOCARE-001
- Conditions
- Infective Endocarditis, Endocarditis, Bacterial, Infection; Heart, Bacteremia, Cardiac Rehabilitation, Nutrition Intervention
- Keywords
- Infective endocarditis, Endocarditis team, Physical Therapy, Individualized Nutritional Support, Probiotic yeast Saccharomyces Boulardii, Cardiac rehabilitation
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Slow recruitment
- Enrolment
- 15 participants (actual)
- Lead sponsor
- Johannes GrandUniversity, hospital or other
- Study start
- 19 Feb 2025 (actual)
- Primary completion
- 7 Dec 2025 (actual)
- Study completion
- 7 Dec 2025 (actual)
- First posted
- 21 Aug 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.
Infective endocarditis (IE) is associated with high morbidity and mortality. Patients with IE are affected by a lengthy hospitalization, leading to physical deconditioning and a rapid decline in physical fitness, muscle mass and strength. Moreover, prolonged antibiotic regimens frequently result in nausea, antibiotic-associated diarrhea and Clostridioides difficile (C.difficile) intestinal infections that further negatively affect patient health. These physical challenges are further exacerbated by the negative impact on mental health, increasing the overall burden of the illness. Implementing a targeted rehabilitative strategy in the hospital setting may therefore improve patient care including physical health and overall quality of life during hospitalization.
Detailed description
BACKGROUND:
Infective endocarditis (IE) is a severe infection of the heart's inner lining, typically the valves, carrying high risks of acute heart failure and death. Patients often face extended hospitalizations (up to six weeks or longer) for intravenous antibiotic treatments, with 30-50% requiring urgent valve surgery. The incidence of IE is 8-10 per 100,000 person-years and rising due to aging populations and increased use of cardiac implantable devices, accounting for 650-700 cases annually in Denmark. Without treatment, mortality is nearly 100%, and with treatment, it ranges from 5-30% during the initial hospitalization, influenced by factors such as infection site, causative agent, age, and comorbidities.
IE significantly impacts patients' health due to prolonged hospitalization. Many experience rapid physical decline, including reduced cardiorespiratory fitness, strength, and overall fitness, caused by bed rest, malnutrition, and limited activity. Recovery is often difficult, with worsening physical, mental, and emotional states. The POET trial found poor self-rated health triples mortality risk. Up to 35% of patients do not return to work, and 65% face readmission within a year. Long hospital stays also increase the need for nursing home care.
Malnutrition is common in IE patients, raising risks of death, illness, and impairment. Acute illness amplifies nutritional deficits, worsening muscle wasting and overall health. The EFFORT trial showed early nutritional support reduces mortality and complications, yet no randomized studies have addressed nutrition in IE patients.
Intravenous antibiotics add distress, often causing nausea, diarrhea, and C. difficile infections. Probiotics like S. boulardii show promise in preventing these side effects.
Cardiac rehabilitation has proven benefits for other heart conditions, improving exercise capacity, quality of life, and reducing readmissions. However, evidence is limited for in-hospital IE rehabilitation. Tailored, supervised programs during hospitalization could address physical and mental health needs, improving overall recovery and quality of life.
PRIMARY AIM:
To investigate the effectiveness of individualized physical rehabilitation and nutritional support designed to reduce physical deconditioning and prevent treatment-related harms thus ultimately improving mental health in patients hospitalized with endocarditis.
HYPOTHESES:
Within a 2-by-2 factorial design, a patient-centered, individualized, and adaptable physical rehabilitation and nutritional plan during lengthy hospitalization will improve mental health more than standard care.
Furthermore, in the same factorial framework, a probiotic supplement during antibiotic-treatment will decrease the rate of antibiotic-associated diarrhea compared to no probiotic supplement.
NUTRITIONAL SUPPORT:
In the intervention group, nutritional screening and support begin within 24 hours of randomization. Individualized nutritional plans are developed based on the NRS 2002 protocol and 2018 international guidelines. A dietitian sets energy requirements using the weight-adjusted Harris-Benedict equation and establishes protein intake targets between 1.2-1.5 g/kg of body weight, adjusting to 0.8 g/kg for patients with acute renal failure.
Patients are screened for risk of refeeding syndrome with routine blood tests, including magnesium, phosphate, and other relevant biomarkers (e.g., bilirubin, creatinine, albumin, electrolytes, etc.). The initial dietary plan includes hospital-provided meals, snacks from an "à la carte" menu, and oral nutritional supplements (ONS). Daily food records monitor intake, and if patients fail to meet 75% of caloric and protein targets for three consecutive days-or earlier based on clinical judgment-escalation to enteral tube feeding or parenteral feeding is initiated.
INDIVIDUALLY PLANNED PHYSICAL EXERCISE BY AN INTERDISCIPLINARY TEAM LEAD BY A SPECIALIZED REHABILITATION PHYSIOTHERAPIST:
The ENDOCARE team, consisting of a cardiologist, nurse, and physiotherapist, optionally involving a family member, will meet with the patient the first weekday after inclusion to design a personalized exercise regimen. This regimen accounts for comorbidities, performance status, disease severity, and support resources. Weekly meetings with the team will address patient concerns and ensure optimal care.
Exercise Modalities
Patients will participate in Intensive Exercise to reduce deconditioning and enhance well-being, focusing on:
Progressive Resistance Exercise: Major muscle groups (e.g., leg presses, arm rows, arm pushes) are targeted with 2-3 sessions/week, using stationary equipment or elastic bands. Training follows a linear progression (3 sets per exercise starting at 15 ± 2 RM, progressing to 10 ± 2 RM) and integrates principles like range of motion and time under tension.
Cardiovascular Exercise: Sessions involve 20 minutes of moderate-intensity exercise (Borg RPE 12-14) 3-4 times/week, using arm ergometers or stationary beds. Intensity and structure (continuous or interval) are adjusted based on patient preference.
Physical Activity Daily physical activity, guided by Danish recommendations (10,000 steps/day), is encouraged using a gradual progression model (e.g., PACE-UP). Activity monitoring is supported by SENS motion accelerometers, with data transferred to a smartphone app. Depending on funding, tablets may provide real-time feedback on activity levels near patient beds.
Control Group Patients in the control group receive standard hospital care, including an initial physiotherapist assessment and 1-2 supervised or self-managed exercise sessions per week.
Risks Potential risks include musculoskeletal injuries (e.g., strains, sprains), fatigue, and overtraining.
GUIDE FOR PROBIOTIC ADMINISTRATION:
In the intervention group, S. boulardii treatment begins at inclusion. Patients will receive Sacchaflor capsules (Pharmaforce Aps), containing S. boulardii (5×10^9 DBVPG 6763 strain) and mannan oligosaccharide (MOS), a supplement derived from Saccharomyces cerevisiae. The capsules are administered twice daily until the end of antibiotic treatment. If the patient is discharged with continued antibiotics, S. boulardii will be used for up to 30 more days.
In the control group, no probiotics will be given for 30 days post inclusion.
Possible side effects include gastrointestinal disturbances (e.g., flatulence, bloating, constipation) and, rarely, fungemia or allergic reactions).
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 4
- Model description
- Investigator-initiated, randomized, single-center, 2-by-2 factorial clinical trial with co-enrolment into two different non-pharmacological interventions. * A combined Intensive physical Therapy and individualised Nutritional Support intervention and administration of probiotic yeast Saccharomyces boulardii * A combined Intensive physical Therapy and individualised Nutritional Support intervention and NO administration of probiotic yeast Saccharomyces boulardii * Administration of probiotic yeast Saccharomyces boulardii and NO Intensive physical Therapy and individualised Nutritional Support. * NO administration of probiotic yeast Saccharomyces boulardii and NO Intensive physical Therapy and individualised Nutritional Support. Patients will receive standard hospital care
| Arm | Type | Receives |
|---|---|---|
| Integrated Physical Therapy and Nutritional Support with Probiotic Saccharomyces boulardii | Active comparator | Behavioral: Intensive physical Therapy, Dietary Supplement: Probiotic treatment, Behavioral: Individualised Nutritional SupportIntensive physical therapy + individualised nutritional support + administration of probiotic yeast saccharomyces boulardii |
| A combined Intensive physical Therapy and individualised Nutritional Support intervention | Active comparator | Behavioral: Intensive physical Therapy, Behavioral: Individualised Nutritional SupportIntensive physical Therapy + Individualised Nutritional Support |
| Administration of probiotic yeast Saccharomyces boulardii | Active comparator | Dietary Supplement: Probiotic treatmentAdministration of probiotic yeast Saccharomyces boulardii |
| Control group | Placebo comparator | Other: Standard hospital careStandard hospital care |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Clinical diagnosis of left-sided (native, prosthetic, or culture-negative) bacterial infective endocarditis mandating iv antibiotic treatment, including Cardiac Implantable Electronic Devices infections, irrespective of cause and location as defined by the ESC modified Duke Criteria
- Age ≥ 18 years
Key exclusion criteria (6 listed)
- Hemodynamic instability (defined as a systolic blood pressure <90 mmHg and lactate >2.2 mmol/l measured in an arterial blood gas.
- Expected to be discharged within 3 days
- Immunocompromised due to severe combined immunodeficiency, HIV, or hematological malignancy
- Fungal endocarditis
- Pregnancy
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 |
|---|---|---|
| Intensive physical TherapyTailored exercise programs supervised by trained physiotherapists, focusing on improving cardiorespiratory fitness, strength, and functional capacity. | Behavioural | A combined Intensive physical Therapy and individualised Nutritional Support intervention, Integrated Physical Therapy and Nutritional Support with Probiotic Saccharomyces boulardii |
| Probiotic treatmentAdministration of probiotic yeast Saccharomyces boulardii twice daily | Dietary supplement | Administration of probiotic yeast Saccharomyces boulardii, Integrated Physical Therapy and Nutritional Support with Probiotic Saccharomyces boulardii |
| Individualised Nutritional SupportPersonalized nutritional plans guided by a dietitian, addressing malnutrition and caloric/protein deficiencies with daily caloric intake adjustments and supplements if necessary based on the EFFORT trial. | Behavioural | A combined Intensive physical Therapy and individualised Nutritional Support intervention, Integrated Physical Therapy and Nutritional Support with Probiotic Saccharomyces boulardii |
| Standard hospital carePatients will receive standard hospital care | Other | Control group |
Primary outcome
Mental health (MH) measured by the standardized Short Form 36 (SF-36)
Time frame: 30 days
Mental Component Summary (MCS) of the Medical Outcome Study Short Form 36 version 2 (SF-36) which has been validated in Danish and in cardiac populations and is widely used in controlled clinical trials. Scores range from 0 to 100, with higher scores indicating better-perceived health
5 secondary outcomes
Change in number of sit and stand in 30 seconds from baseline to 14 days
Time frame: 14 days
Quality of life from EQ-5D
Time frame: 14, 30, and 90 days follow-up
Days alive without diarrhea
Time frame: 30 days in hospital and 90 days out of hospital
Days alive and out of hospital
Time frame: 30 day in hospital, and 90 day out-of-hospital
All-cause mortality
Time frame: 30 days
Results and safety
The study was stopped early (reason given: Slow recruitment). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Dec 2025.
- Individual participant dataSharing planned: Yes. Individual participant data that underlie the results reported in the publication will be shared. Data will be available beginning after publicatoin of the main papers. Access will be granted to researchers who provide a methodologically sound proposal, which will be reviewed by the national governing body for approval both regarding ethics and patients data safety.
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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. This study is not recruiting at the moment.
Johannes Grand, MD, PhD principal investigator
Copenhagen University Hospital Amager-Hvidovre, Department of Cardiology
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intensive physical Therapy, Probiotic treatment and Individualised Nutritional Support in people with Infective Endocarditis and Endocarditis, Bacterial, run by Johannes Grand at 1 site in Denmark.
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 2 inclusion and 6 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: stopped early, as of the sponsor's last update on 15 Dec 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 Denmark. 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. Some participants in this study may receive a placebo. 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?
The study was stopped early (reason given: Slow recruitment). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mental health (MH) measured by the standardized Short Form 36 (SF-36) (time frame: 30 days). 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 15 Dec 2025.