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NCT06424769Enrolling by invitation

Improving Outcomes and Reducing Disparities for Patients With Inflammatory Bowel Disease Through Epidemiology and Enhanced Disease Management

Improving Outcomes and Reducing Disparities for Patients With Inflammatory Bowel Disease Through Epidemiology and Enhanced Disease Management (PROMOTE IBD)

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

The goal of this clinical trial is to learn whether IBD patients have better disease outcomes and feel more empowered to manage their condition if they have access to text messaging with their clinical team and if their symptoms are more regularly monitored through text-based surveys. Researchers will compare participants who have access to text-based monitoring, communication and education to participants who have access to text-based education alone. Researchers will also examine if different social and other non-medical factors impact IBD symptoms and quality of life. All participants will: * complete 5 brief on-line surveys over 12 months about their IBD and social risk factors, * receive IBD education content by text message up to 2 times a week. Some participants will also: * receive additional surveys by text to monitor their IBD progression, * have the opportunity to directly text message their IBD medical team.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
900 (estimated)
First submitted
13 May 2024
Start date
24 Jul 2024
Primary completion date
Sept 2028
Lead sponsor
University of North Carolina, Chapel Hill
NCT number
NCT06424769

What you commit to

  • Study type: Interventional
  • Planned participants: 900
  • From 24 Jul 2024 to the primary completion date, Sept 2028
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • IBD patients s/p surgery with a current pouch or ostomy.

Other

  • Unable to provide informed consent and child assent for minors.

Who the study is looking for

  • 13+ years old with IBD (Crohn's disease, ulcerative colitis, indeterminant colitis).
  • Followed at a participating site with an office visit (in-person or virtual) within the preceding 12 months.
  • Have access to a mobile phone and willing and able to receive and respond to text messages.
  • Willing to answer questions on electronic surveys.
  • Have the ability to read text messages and answer surveys in English or Spanish.

Age in the registry: 13 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Morehouse School of Medicine
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Boston Medical Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
UNC-Chapel Hill School of Medicine
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status
Atrium Health Levine Children's
Coordinator of this site? Confirm its status
CharlotteUnited StatesUnknown status
NYU Langone Health Lake Success
Coordinator of this site? Confirm its status
Lake SuccessUnited StatesUnknown status
University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
University of California San Diego
Coordinator of this site? Confirm its status
San DiegoUnited StatesUnknown status
University of California San Francisco-Benioff Children's Hospital
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status
Mayo Clinic - Arizona
Coordinator of this site? Confirm its status
ScottsdaleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.