Testing the Impact of Measurement-Based Care on Quality of Life and Disease Management Among Veterans With Inflammatory Bowel Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVA Office of Research and Development

About this trial

This research study is addressing issues related to Inflammatory bowel disease (IBD), which is a chronic autoimmune disorder that affects over 60,000 Veterans. With close monitoring and timely treatment adjustment, the investigators can stop the natural progression of IBD, improving health-related quality of life (HRQOL) and reducing flares and hospitalizations. However, it is difficult to closely monitor Veterans with IBD between clinic visits. There is a critical need for solutions that support close between visit monitoring of Veterans with IBD. The Measurement-Based Care (MBC) for IBD study will take a systematic approach to collect, share, and act on patient reported outcome (PRO) data that can be used to achieve close monitoring. MBC supports patients' in managing their condition and boosting their confidence in their ability to handle their symptoms and disease, and also supports care teams in early recognition of health issues. The investigators will work with both Veterans and their care teams to understand and assess this program so it can be a model for future initiatives.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

receiving IBD care at one of the four sites

reporting an impaired IBD-specific HRQOL using the Short IBD Questionnaire (SIBDQ<60, as used by others)

willingness and ability to participate in study procedures

relevant clinic staff (gastroenterologists, advanced practice providers, nurses) involved in MBC in IBD at the four study sites (Ann Arbor, Atlanta, Houston, Portland).

Disqualifiers

Presence of an ostomy or ileal-pouch anal anastomosis

Severe comorbid medical condition that can confound PRO scores and treatment priorities (e.g., cancer, transplant).

Exclusions can be readily determined from chart review and a baseline patient assessment

Clinic staff without any experience with MBC in IBD.

Trial design

Design model

Parallel

Treatments tested in this trial

  • MBC-IBD Intervention

    Behavioral

    Measurement Based Care for Inflammatory Bowel Disease - Intervention group. Veteran participants who are randomized to 12-months of MBC-IBD will be enrolled for 12 months. They will each complete surveys at baseline, 6-months, and 12-months post-randomization. After baseline completion, participants will be asked to complete weekly surveys. These assessments require completion of self-report questionnaires (PROs) which will be completed by phone or electronically using VA REDCap. MBC in IBD will not replace but rather provide care continuity between clinic visits. Patients allocated to MBC in IBD will receive automated reminders to complete weekly questionnaires. Further, patients will receive quarterly reports of their PRO data trends.

  • Enhanced Treatment as Usual (E-TAU)

    Other intervention

    E-TAU will receive standard of care, including monitoring and treatment as directed at the discretion of their gastroenterologist. Participants will also receive educational videos and fact sheets on various IBD-specific topics.

Treatment groups

250 Participants
are divided into 2 treatment groups
Group A: MBC-IBDExperimental treatment 1 intervention
Group B: E-TAUActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Patient-reported Health-related Quality of Life

Test the effectiveness of MBC vs. E-TAU on key patient outcomes, specifically looking at IBD-specific patient reported HRQOL (primary outcome). Assess IBD-specific HRQOL compared to E-TAU at 12-months follow-up. The investigators will first graphically explore the longitudinal data over time between the MBC and E-TAU groups. As the primary analytic model, the investigators will use an analysis of covariance (ANCOVA), fit using a linear regression model with SIBDQ score at 12 months as the dependent variable to estimate between-group differences in the primary endpoint. The model will include an indicator for treatment group (MBC vs. E-TAU) to estimate the 12-month treatment effect and adjust for baseline SIBDQ scores as a covariate and the stratification factors used for randomization (site, age, IBD type).

Time frame
Baseline compared to 12 month follow-up.

Secondary outcomes

1

IBD-related events

Review of IBD-related events obtained via electronic health record data: The investigators will first assess the total count of flares, emergency department visits, hospitalizations, and surgeries between baseline and 12 months and model cumulative composite outcomes at 12-months. If the total outcome counts are low (mostly 0's or 1's), the investigators will use a logistic regression model to model a dichotomized outcome. If the total counts have a range (e.g., 0 to 5 or more), the investigators will use a count data model such as Poisson or negative binomial regression model. The investigators will include intervention group (MBC vs. E-TAU) as the primary predictor, as well as study site, age, IBD type, and other covariates that show imbalances in baseline analyses.

Time frame
Baseline compared to 12 month follow-up.

Other outcomes

Sponsors and contacts

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