A care pathway for managing irritable bowel syndrome and GI disorders
Official title: GUT LINK: A Pilot Study to Evaluate the Comparative Effectiveness of an Evidence-based Care Pathway Across Primary and GI Specialty Care
Run by Nova Scotia Health Authority · NCT05725954 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing a new care plan to help doctors better diagnose and treat irritable bowel syndrome and other gut issues using a special support tool.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Nova Scotia Health Authority Academic / other |
| Locations | 1 site (Halifax, Nova Scotia) |
| Trial ID | NCT05725954 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are general practitioners in Nova Scotia who treat patients with lower GI complaints and use the 'virtual hallway' platform for referrals.
✕Probably not a fit
Patients who do not have access to primary care or those with severe gastrointestinal conditions requiring immediate specialist intervention may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to implement and evaluate a Clinical Care Pathway designed to assist primary healthcare providers in diagnosing and managing irritable bowel syndrome (IBS) and other gastrointestinal disorders. By utilizing evidence-based guidelines, the study seeks to improve the differentiation between IBS and more serious gastrointestinal conditions. The intervention involves the GUT LINK SmartPath platform, which supports healthcare providers in delivering care to patients with lower GI complaints. The pilot study will assess the effectiveness of this care pathway in a real-world setting.
Why it matters
Potential benefit: If successful, this approach could enhance the accuracy of IBS diagnoses and improve patient management in primary care settings.
How similar studies have gone: While the approach of implementing care pathways is established, this specific study's focus on IBS and GI disorders through a virtual platform is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Must be a general practitioner * Have a family practice in Nova Scotia, Canada * Utilize the platform 'virtual hallway' as part of current referral practices * Deliver care to patients with lower GI complaints Exclusion Criteria: * None
Where it's running
-
QEII Health Sciences Centre
Halifax, Nova Scotia, Canada Recruiting
Study contacts
- Study coordinator: Michael Stewart, MD
- Email: Michael.Stewart@Dal.ca
- Phone: 1(902) 473-2222 xt. 2526
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Liver Fat and Scarring in People Suspected of Non-Celiac Wheat Sensitivity
This study looks to see if people with non-celiac wheat sensitivity have liver fat or fibrosis and how this relates to IBS/FD and celiac disease.
-
Repeated transcranial magnetic stimulation to treat diarrhea-predominant irritable bowel syndrome
This study will test whether repeated transcranial magnetic stimulation (rTMS) can reduce diarrhea, abdominal pain, and improve quality of life in adults with IBS-D.
-
Brenipatide (LY3537031) for IBS with constipation
This trial will test whether brenipatide (LY3537031), given by a small under-the-skin injection, helps adults with IBS-C have less belly pain and more normal bowel movements compared with a placebo.
-
Brenipatide (LY3537031) treatment for adults with IBS‑D
This will test whether brenipatide (LY3537031) given under the skin helps adults with IBS‑D reduce belly pain and improve stool consistency compared with placebo.
-
Camlipixant for IBS-D and IBS-M: a test in adults
This study tests camlipixant versus placebo in adults with IBS with diarrhea or mixed IBS to see if it helps reduce symptoms and is safe.
-
Defining Objective Markers of Dietary Compliance in IBS
This study tests whether a biomarker in stool or urine can reflect how much certain carbohydrates you eat, helping manage IBS.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.