Official Title
The Effects of 3-month Supplementation With a Pre-probiotic on Patient- and Clinician-reported Outcomes, and Brain Tissue Metabolism in Patients With Post-covid Fatigue Syndrome: a Placebo-controlled Randomized Clinical Trial
Brief Summary

The goal of this randomized controlled double-blind parallel-group interventional trialis to evaluate the effects of of dietary supplementation with a pre-probiotic on patient-and clinician-reported outcomes, and brain tissue metabolism in patients with post-covidfatigue syndrome.

Detailed Description

Not Provided

Completed
Long Covid

Dietary Supplement: Dietary Supplement: Experimental

Combination of pre-probiotic

Dietary Supplement: Dietary Supplement: Placebo

Inert compound

Eligibility Criteria

Inclusion Criteria:

- Age 18 - 65 years

- Covid-19 positive test within last 3 months (as documented byvalid PCR or
antigentest

- Moderate-to-severe fatigue (20-MFI test total score > 43.5)

- At least one of additional covid-19 related symptoms
(anosmia,ageusia,breathingdifficulties,lungpain, body aches, headaches, difficulties
concentrating etc.)

Exclusion Criteria:

- Other pulmonary and cardiovascular conditions

- History of dietary supplement use during the past 4 weeks

- Organic gastrointestinal (GI) disorders such as inflammatory bowel disease, coeliac
disease, eosinophilic disorders, or current infection of the GI tract.

- Bowel surgery or short bowel syndrome.

- Medication or supplement which can impact the gut microbiome, including:
antibiotics, antimicrobials, or antifungals in the two months

- Probiotic or prebiotic supplements in the last 4 weeks

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 65 Years
Countries
Serbia
Locations

Applied Bioenergetics Lab at Faculty of Sport and PE
Novi Sad 3194360, Vojvodina 784272, Serbia

Not Provided

University of Novi Sad, Faculty of Sport and Physical Education
NCT Number
Keywords
Prebiotic
Probiotic
Metabolism
Fatigue
MeSH Terms
Post-Acute COVID-19 Syndrome
Fatigue