Can breathing and meditation ease PBC symptoms? new study says maybe.
NCT ID NCT06861465
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a 10-week online wellness program for women with primary biliary cholangitis (PBC), a chronic liver disease that causes fatigue, itching, brain fog, and emotional distress. The program included guided breathing, meditation, gentle movement, and optional nutrition advice. Researchers wanted to see if it was practical and helpful for managing symptoms and improving quality of life.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Jul 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 to 75 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Primary Biliary Cholangitis (PBC) as confirmed by a study Hepatologist using accepted clinical criteria * Have been on stable medical therapy for PBC for ≥3 months * Score ≥3 on a 1-10 numeric rating scale for two of: depression, anxiety, fatigue, sleep disturbance, cognitive impairment * Are able to communicate in English * Have access to an Internet-connected device in their home * Can commit to up to 60 minutes of study activities 5 days per week Exclusion Criteria: * Unable to provide informed consent * Have decompensated cirrhosis including hepatic encephalopathy * Are post-liver transplant * Current severe substance use or psychiatric disorder judged to interfere with study testing or program participation * Are receiving compassionate care * Have a clinical condition that makes the intervention unsafe or infeasible (e.g. unable to follow instruction) or unsafe environment for virtual participation * Practices mind-body practices more than the study dose * Have contraindications for MRI * Have colour blindness * Are unable to attend baseline testing
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Alberta
Edmonton, Alberta, T6G 2X8, Canada
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