NCT07161245 RELIEF: Multimodal Prehabilitation to Treat Fatigue in Patients With Primary Biliary Cholangitis
| NCT ID | NCT07161245 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Hospital Clinic of Barcelona |
| Condition | Primary Biliary Cholangitis (PBC) |
| Study Type | INTERVENTIONAL |
| Enrollment | 64 participants |
| Start Date | 2025-02-06 |
| Primary Completion | 2026-09-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 64 participants in total. It began in 2025-02-06 with a primary completion date of 2026-09-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The implementation of a non-pharmacological multimodal intervention program-including physical exercise, nutritional counseling, and psychological support-is expected to improve fatigue in patients with primary biliary cholangitis. Consequently, this improvement is anticipated to enhance quality of life and cognitive symptoms, while also positively impacting emotional, social, and occupational aspects. From a pathophysiological perspective, it is hypothesized that chronic cholestasis and/or immune system activation, with the release of pro-inflammatory cytokines, leads to both central and peripheral alterations causing fatigue. At the central level, systemic inflammation may induce neuronal senescence in the basal ganglia, resulting in altered functional connectivity networks dependent on these regions and/or structural and connectivity changes in areas involved in interoception, such as the insula and anterior cingulate cortex. At the peripheral level, the hypothesis is that chronic inflammation mediated by anti-mitochondrial antibodies causes mitochondrial metabolic dysfunction in muscle cells, which would be reflected in changes observed in the gene expression analysis of these cells. Improvement in fatigue following the multimodal intervention program is expected to be associated with normalization of the immunological profile, enhanced functional brain connectivity, and improved mitochondrial metabolism in muscle.
Eligibility Criteria
Inclusion Criteria: * Age ≥18 years * PBC diagnosis according to EASL guidelines * Moderate - severe fatigue defined by ≥ 29 points in PBC-40 questionnaire Exclusion Criteria: * Age \> 80 years * Severe pruritus * Decompensated cirrhosis * Other causes of liver disease than PBC * Liver transplant (LT) o placement on a waiting-list for LT * Uncontrolled thyroid disesase * Anemia with haemoglobin \<11g/dl * Uncontrolled cardiovascular risk factors * BMI \> 35, * Acute myocardial infarct or unstable angina the past 6 months * Muscle disease or systemic disease with potential muscle involvement * Dysautonomy * Untreated osteoporosis * Untreated celiac disease * Alcohol consumption \> 14 standard drinks (SD) in women and \>21 (SD) in men per week * Chronic kidney disease ≥ 4 KDIGO stage * Malignancy in the past two years (except for non melanoma skin cancer and in situ cervical carcinoma) * Not capable of performing or following the prehabilitation program * Involvement in a clinical trial the previous 2 months * Refusal of informed consent For the study of the pathophysiology of fatigue, additional exclusion criteria will be established: Severe depression or neuropsychiatric disease, 2) Treatment with centrally acting drugs, 3) Muscular or systemic disease with potential muscle involvement, 4) Immunosuppressive treatment, 5) Sleep disorder, 6) Obesity (BMI \>30).
Contact & Investigator
Sergio Rodríguez Tajes, MD, PhD
PRINCIPAL INVESTIGATOR
Hospital Clinic of Barcelona
Frequently Asked Questions
Who can join the NCT07161245 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Primary Biliary Cholangitis (PBC). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07161245 currently recruiting?
Yes, NCT07161245 is actively recruiting participants. Contact the research team at HEHERNANDEZ@clinic.cat for enrollment information.
Where is the NCT07161245 trial being conducted?
This trial is being conducted at Barcelona, Spain.
Who is sponsoring the NCT07161245 clinical trial?
NCT07161245 is sponsored by Hospital Clinic of Barcelona. The principal investigator is Sergio Rodríguez Tajes, MD, PhD at Hospital Clinic of Barcelona. The trial plans to enroll 64 participants.