Inflammatory Bowel Disease Clinical Trial
Official title:
Specialty Medical Homes to Improve Outcomes for Patients With IBD and Behavioral Health Conditions
Verified date | March 2024 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A comparative effectiveness study using an individual-level randomized design along with a pragmatic, mixed-methods approach to compare two strategies (e.g. in-person supported care, technology-supported care) all of which include evidence-based components for delivering IBD and BH care. Quantitative (e.g. self-report, electronic health record, process) and qualitative (e.g., interviews) data will be collected across multiple time points during the study period.
Status | Active, not recruiting |
Enrollment | 658 |
Est. completion date | September 30, 2026 |
Est. primary completion date | February 28, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Inflammatory Bowel Disease Diagnosis of Crohn's or Ulcerative Colitis. Behavioral health symptoms mild to severe, defined as a score of >= 6 on the Personal Health Questionnaire 4 (PHQ4) Exclusion Criteria: - Lack of smart phone, and/or are unable to speak, read or understand English at the minimum-required level. |
Country | Name | City | State |
---|---|---|---|
United States | University of Pittsburgh Medical Center | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh | Mount Sinai Hospital, New York, Patient-Centered Outcomes Research Institute, The Cleveland Clinic |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Inflammatory Bowel Disease Symptom Severity-PROMIS GI | Patient-Reported Outcomes Measurement Information System Gastrointestinal (PROMIS GI symptoms scale) | Compare at Baseline, 6-month and 12-month for any changes | |
Primary | Inflammatory Bowel Disease Symptom Severity-HBI | Harvey Bradshaw Index | Compare at Baseline, 6-month and 12-month for any changes | |
Primary | Inflammatory Bowel Disease Symptom Severity | Ulcerative Colitis Activity Index | Compare at baseline, 6-months and 12-months for any changes | |
Primary | Behavioral Health Symptom Severity | Personal Health Questionnaire (PHQ-8) | Compare at baseline, 6-month and12-month for any changes | |
Primary | Behavioral Health Symptom Severity | General Anxiety Disorder 7 item scale (AD-7) | Compare at baseline, 6-month and 12-months for any changes | |
Secondary | Functional Impairment | Short Form 12 Health Survey Version 2- (SF12V2) | Compare at baseline, 6-month and 12-month for any changes | |
Secondary | Health Care Utilization | Composite score of Emergency Department visits, unplanned hospitalizations, surgeries, procedures/imaging | Compile and compare at baseline, 6-month and 12-months for any changes | |
Secondary | Self-Efficacy | Inflammatory Bowel Disease Self-Efficacy Scale | Compare at baseline, 6-month and 12-month for any changes | |
Secondary | Inflammatory Bowel Disease- Related Quality of Life | Short Quality of Life in Inflammatory Bowel Disease Questionnaire- SIBDQ | Compare at baseline, 6-month and 12-month for any changes |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT03278912 -
Natural History of Intestinal Inflammation in People With Primary Immune Dysregulations
|
||
Terminated |
NCT00061282 -
Clotrimazole Enemas for Pouchitis in Children and Adults
|
Phase 1/Phase 2 | |
Recruiting |
NCT05579392 -
A Randomized Crossover Trial of Bright Light Therapy in Crohn's Disease on Intestinal Barrier Homeostasis
|
N/A | |
Completed |
NCT03264690 -
Study to Observe the Change in Microbiome in Human Derived Sample and the Relation With Clinical Response Before and After the Anti-TNF Treatment in IBD Patients
|
||
Recruiting |
NCT02861053 -
Inflammatory Bowel Disease : Could a Regular Physical Activity Reduce Patients Fatigue ?
|
N/A | |
Recruiting |
NCT02275676 -
Resting Energy Expenditure and Nutritional Status in IBD
|
N/A | |
Completed |
NCT02161640 -
Vascular Dysfunction in Paediatric IBD
|
N/A | |
Completed |
NCT02503696 -
Sample Collection Study to Evaluate DNA Markers in Subjects With Inflammatory Bowel Disease (IBD)
|
N/A | |
Completed |
NCT02197780 -
Head-to-head Comparison of Two Fecal Biomarkers to Screen Children for IBD
|
N/A | |
Completed |
NCT01852760 -
Assessment of Disease Activity in Ulcerative Colitis by Endoscopic Ultrasound
|
N/A | |
Completed |
NCT01933867 -
Water-aided Colonoscopy in Inflammatory Bowel Disease Patients
|
N/A | |
Completed |
NCT01860651 -
Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease
|
N/A | |
Completed |
NCT01692743 -
Telemedicine in Patients With Inflammatory Bowel Disease (TELE-IBD)
|
Phase 3 | |
Completed |
NCT01688557 -
Trial on Innovative Technologies in Colonoscopy
|
N/A | |
Completed |
NCT01666535 -
Infliximab IBD Influenza Vaccine Study
|
N/A | |
Completed |
NCT01676324 -
FOCUS: The Future of Fecal Calprotectin Utility Study for the Diagnosis and Management of Inflammatory Bowel Disease (IBD)
|
N/A | |
Completed |
NCT01981616 -
Immune Response to Systemic and Mucosal Antigenic Challenge in the Presence of Vedolizumab
|
Phase 1 | |
Completed |
NCT01557387 -
Real-time Diagnosis of Pseudopolyps During Colonoscopy
|
||
Completed |
NCT01476995 -
Prognostic Indicators as Provided by the EPIC ClearView
|
N/A | |
Completed |
NCT01221818 -
A Randomized, Double-Blind, Placebo-Controlled, Ascending Single Dose Study of E6007 in Healthy Subjects
|
Phase 1 |