Inflammatory Bowel Diseases Clinical Trial
— PATIENT-UCOfficial title:
Patient Centered Algorithms to Optimize the Inpatient Experience and Treatment of Ulcerative Colitis: PATIENT-UC
Verified date | February 2020 |
Source | Mount Sinai Hospital, Canada |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hospitalized patients with ulcerative colitis (UC) are at increased risk for a variety of complications such as infections, venous thrombosis, and surgery. The literature has revealed significant variation in the quality of care to hospitalized UC patients. As a result, guidelines for the management of these patients have been developed. However, the update of guidelines are variable. Admission to hospital can also have significant impact on quality of life due to interruptions in life commitments and lost sense of control of disease. Maintaining a sense of self-control of disease and active participation in care has been shown to be valuable among individuals with chronic diseases. The investigators propose the development of a multi-site, patient centred initiative aimed at improving clinical and patient-centered outcomes through an educational iPad based tool for patients admitted to hospital with ulcerative colitis.
Status | Completed |
Enrollment | 91 |
Est. completion date | January 2020 |
Est. primary completion date | January 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - diagnosis of ulcerative colitis - able to provide informed consent - admission to hospital with flare of underlying ulcerative colitis Exclusion Criteria: - Crohn's disease - inability to provide informed consent - readmission during study period (intervention would only be used on the initial admission during the study period) |
Country | Name | City | State |
---|---|---|---|
Canada | Mount Sinai Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Mount Sinai Hospital, Canada | Dalhousie University, McGill University, University of Alberta, University of British Columbia, University of Calgary, University of Manitoba, University of Ottawa |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Proportion of patient undergoing testing of C difficile within 48 hours of admission | 1 year | ||
Other | Time from initiation of IV steroids to salvage therapy or surgery. | 1 year | ||
Other | Proportion of patients receiving VTE prophylaxis | 1 year | ||
Other | Trust in physician as measured by TIPS | 6 months | ||
Other | Patient Satisfaction as measured by CACHE | 6 months | ||
Other | Anxiety and Depression as measured by HADS. | 6 months | ||
Other | Adherence to Medication as measured by Morisky scale | 6 months | ||
Primary | Overall length of stay | 1 year | ||
Primary | Percentage of patients undergoing colectomy | 1 year |
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