Ulcerative Colitis Clinical Trial
Official title:
Counseling to Optimize Medication Adherence in Expectant Mothers With Inflammatory Bowel Disease (COACH-IBD)
Inflammatory Bowel Disease (IBD) is a chronic inflammatory disorder of the gastrointestinal
tract that comprises two subtypes, Crohn's disease (CD) and Ulcerative Colitis (UC). Because
the risk of IBD is greatest during the third decade of life, its impact for women is during
the reproductive years. Women with inflammatory bowel disease are at a 2-fold higher risk of
adverse outcomes during pregnancy as compared to the general population. Pregnancy is an
especially vulnerable time for women with IBD, and out of misguided concerns that medications
may confer unnecessary harms to their fetus, many women often stop taking life savings
medications; without realizing that this sub-optimal adherence could actually lead to life
threatening complications for them and their fetus. Counseling pregnant women with IBD is
therefore an important step in improving medication adherence. The investigators hypothesize
that counseling sessions with an IBD nurse that incorporates motivational interviewing and
telemedicine-based follow-up sessions tailored to individual needs will improve medication
adherence and pregnancy outcomes.
The following specific aims are to be addressed by this multi-center randomized clinical
trial comparing individual nurse-based counseling to standard of care:
Specific Aim #1: To assess whether patient-centered counseling incorporating motivational
interviewing and telemedicine-based follow-up by an IBD nurse leads to improved medication
adherence during pregnancy and pregnancy outcomes
Specific Aim #2: To validate the use of self-reported medication adherence during pregnancy
in the IBD population
Status | Recruiting |
Enrollment | 220 |
Est. completion date | October 1, 2020 |
Est. primary completion date | October 1, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Have a confirmed diagnosis of IBD - Expected to be on an IBD-related medication throughout pregnancy - In First Trimester of Pregnancy - Willing to undergo pregnancy counseling with close monitoring - Able to provide informed consent Exclusion Criteria: - Patients who are not residing in Ontario of Alberta - Unconfirmed diagnosis of IBD - In Second or Third Trimester of Pregnancy - Uncertainty regarding whether IBD medication will be prescribed throughout pregnancy - Unwilling to participate - Inability to provide informed consent |
Country | Name | City | State |
---|---|---|---|
Canada | University of Calgary | Calgary | Alberta |
Canada | Mount Sinai Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Mount Sinai Hospital, Canada | Crohn's and Colitis Canada |
Canada,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Medication Adherence (MARS-5) | Comparison of medication adherence as a dichotomous outcome (adherent vs. non-adherent) using the chi-square statistic between intervention and control groups. | Comparison of dichotomous variable at Baseline and Gestational Week 34 | |
Secondary | IBD-Specific Health Related Quality of Life (IBDQ) | Comparison of IBDQ as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | PRO-2 Scale for Crohn's Disease related disease activity | Comparison of scores on the PRO-2 scores as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | 6-Point Mayo Score for Ulcerative Colitis related disease activity | Comparison of 6-Point Mayo Score as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | Patient Trust in Physician (TIPS) | Comparison of TIPS as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | Patient Satisfaction (CACHE) | Comparison of CACHE as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | IBD Specific Knowledge (CCKNOW) | Comparison of CCKNOW as a continuous variable using the the Mann-Whitney test between intervention and control groups. | Comparison of continuous variable at Baseline Gestational Week 34 | |
Secondary | Fecal Calprotectin | Comparison of proportion of subjects with elevated fecal calprotectin scores, as an objective measure of inflammation and disease activity, between study groups using chi-square statistic. | Comparison of dichotomous outcome at Baseline and Gestational Week 34 | |
Secondary | Preterm Delivery | Gestational age recorded at delivery will be used to ascertain preterm delivery (<37 weeks) and compare rates of preterm delivery between study groups using chi-square statistic. | Comparison of dichotomous outcome at Delivery | |
Secondary | Small for Gestational Age | Birth weight recorded at delivery will be used to ascertain whether infants are small for gestational age and compare rates of small for gestational age infants at delivery between study groups using chi-square statistic. | Comparison of dichotomous outcome at Delivery |
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