Trial of a Treatment Algorithm for the Management of Crohn's Disease (REACT)
Primary Purpose
Crohn's Disease
Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Treatment Algorithm for Crohn's Disease
Sponsored by
About this trial
This is an interventional treatment trial for Crohn's Disease focused on measuring Crohn's disease, community based gastroenterology practices Canada and Belgium, Cluster randomization controlled trial, Remission, Corticosteroids, Documented diagnosis of Crohn's disease
Eligibility Criteria
Inclusion Criteria:
- Documented diagnosis of Crohn's disease
- Able to speak and understand English, French or Flemish
- Access to a telephone or email/internet service
- Written informed consent must be obtained and documented
Exclusion Criteria:
- Any conditions (e.g., history of alcohol or substance abuse) which in the opinion of the investigator , may interfere with the patients ability to comply with study procedures
- Participating in other investigational studies
Sites / Locations
- Robarts Clinical Trials, Robarts Research Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Usual Care practice
Treatment Algorithm
Arm Description
Patients managed according to usual care practices
Practitioners assigned to the intervention arm will be educated on the use of the treatment algorithm.
Outcomes
Primary Outcome Measures
Proportion of patients in remission at the end of the 24 month followup period. Remission is defined as a HBS< or = 4 without use of steroids for the treatment of CD. the primary analysis will be performed at the level of the practice.
Secondary Outcome Measures
Proportion of patients in remission over study, change in mean HBS; use of CD meds, occurrence of surgery/hospitalization for CD and complications, patients' health related QOL measured by SF-36 & EQ-5D; physician/patient satisfaction with therapy.
Full Information
NCT ID
NCT01030809
First Posted
December 9, 2009
Last Updated
March 19, 2014
Sponsor
University of Western Ontario, Canada
Collaborators
Abbott
1. Study Identification
Unique Protocol Identification Number
NCT01030809
Brief Title
Trial of a Treatment Algorithm for the Management of Crohn's Disease
Acronym
REACT
Official Title
A Cluster Randomized Controlled Trial of a Treatment Algorithm for the Management of Crohn's Disease
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Western Ontario, Canada
Collaborators
Abbott
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Assess if the implementation of a treatment algorithm will improve the management of Crohn's disease (CD) in comparison to usual care based gastroenterology practices.
Detailed Description
Crohn's disease (CD) is a chronic inflammatory disorder of the gastrointestinal tract. During disease exacerbations, pharmacological or surgical intervention is usually needed to re-establish remission. Ideally, strategies should be employed to maintain patients in long-term remission while minimizing exposure to corticosteroids and reduce therapy-related toxicity.
Nevertheless, in reality many patients with CD do not receive effective therapy and their disease often remains active, leading to uncontrolled inflammation and complications from either the underlying disease or corticosteroids. Although treatment guidelines exist, they do not adequately define treatment goals and the duration of treatment cycles is not specified Optimizing outcomes in CD requires rapid control of inflammation. Intuitively, persistent inflammation leads to persistent symptoms, tissue damage, and disease-related complications. Conventional therapy is frequently ineffective in moderate to severe CD, and is often continued for a prolonged time. Consequently, many patients are under-treated. An alternate strategy that minimizes the use of corticosteroids and encourages the earlier use of immunosuppressive agents and tumour necrosis factor (TNF) antagonists may be optimal. However it is unknown whether this approach is superior to usual care
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Crohn's disease, community based gastroenterology practices Canada and Belgium, Cluster randomization controlled trial, Remission, Corticosteroids, Documented diagnosis of Crohn's disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1999 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Usual Care practice
Arm Type
No Intervention
Arm Description
Patients managed according to usual care practices
Arm Title
Treatment Algorithm
Arm Type
Active Comparator
Arm Description
Practitioners assigned to the intervention arm will be educated on the use of the treatment algorithm.
Intervention Type
Other
Intervention Name(s)
Treatment Algorithm for Crohn's Disease
Intervention Description
Practitioners assigned to the intervention arm will be educated on the use of the treatment algorithm.
Primary Outcome Measure Information:
Title
Proportion of patients in remission at the end of the 24 month followup period. Remission is defined as a HBS< or = 4 without use of steroids for the treatment of CD. the primary analysis will be performed at the level of the practice.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Proportion of patients in remission over study, change in mean HBS; use of CD meds, occurrence of surgery/hospitalization for CD and complications, patients' health related QOL measured by SF-36 & EQ-5D; physician/patient satisfaction with therapy.
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Documented diagnosis of Crohn's disease
Able to speak and understand English, French or Flemish
Access to a telephone or email/internet service
Written informed consent must be obtained and documented
Exclusion Criteria:
Any conditions (e.g., history of alcohol or substance abuse) which in the opinion of the investigator , may interfere with the patients ability to comply with study procedures
Participating in other investigational studies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian G Feagan, MD
Organizational Affiliation
Robarts Research Institute - University of Western Ontario
Official's Role
Principal Investigator
Facility Information:
Facility Name
Robarts Clinical Trials, Robarts Research Institute
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5K8
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
30891808
Citation
Singh S, Stitt LW, Zou G, Khanna R, Dulai PS, Sandborn WJ, Feagan BG, Jairath V. Early combined immunosuppression may be effective and safe in older patients with Crohn's disease: post hoc analysis of REACT. Aliment Pharmacol Ther. 2019 May;49(9):1188-1194. doi: 10.1111/apt.15214. Epub 2019 Mar 19.
Results Reference
derived
PubMed Identifier
26342731
Citation
Khanna R, Bressler B, Levesque BG, Zou G, Stitt LW, Greenberg GR, Panaccione R, Bitton A, Pare P, Vermeire S, D'Haens G, MacIntosh D, Sandborn WJ, Donner A, Vandervoort MK, Morris JC, Feagan BG; REACT Study Investigators. Early combined immunosuppression for the management of Crohn's disease (REACT): a cluster randomised controlled trial. Lancet. 2015 Nov 7;386(10006):1825-34. doi: 10.1016/S0140-6736(15)00068-9. Epub 2015 Sep 3.
Results Reference
derived
Learn more about this trial
Trial of a Treatment Algorithm for the Management of Crohn's Disease
We'll reach out to this number within 24 hrs