Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease
Primary Purpose
Inflammatory Bowel Disease, Ulcerative Colitis, Crohn´s Disease
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Web-monitoring
Sponsored by
About this trial
This is an interventional supportive care trial for Inflammatory Bowel Disease focused on measuring Inflammatory Bowel Disease, Ulcerative Colitis, Crohn´s Disease, Children, Adolescence, E-health web-monitoring, Adherence, Disease activity, Fecal Calprotectin
Eligibility Criteria
Inclusion Criteria:
- IBD diagnosis according to the Copenhagen and Porto criteria
- Aged between 10-17 years
- Fluent in Danish
- Access to the internet
- Patients in treatment with infliximab must have completed the induction period (i.e. minimum six week after start-up of treatment).
Exclusion Criteria:
- Insufficient Danish language skills
- Lack of intellectual capacity
- Growth retardation
Sites / Locations
- Department of Pediatrics, Hvidovre Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Web-monitoring
Control
Arm Description
There is two arms for intervention: 1) Patients in treatment with medicine administrated at home and 2) patients in treatment with biologicals.
Patients in treatment with medicine administrated at home: routine outpatient controls, four times a year. Patients in treatment with biologicals: retrospective routine treatment algorithm
Outcomes
Primary Outcome Measures
Medical Adherence
Participants (group 1, medication adm. at home): Medicine Adherence Report Scale (MARS): range 5-25 points. Higher scores mean a better outcome. In the below Outcome Measure Data Table the mean data for each group (web and control) summarized from the whole study periode are presented.
Secondary Outcome Measures
Number of Participants With Step up in Medical Intensity
Time to frist step-up in treatment intensity (escalating dose or change/addition of a more potent drug) were obtained from the patient's medical record during the study period, as a proxy of progression in disease activity.
Time to step up was analysed via Kaplan Meier survival analysis.
Surgery
Need for surgery
Absence From School
Number of days absence from school
Contact to the Hospital
Need for outpatient visits
Number of Weeks Between Treatment
Date of IFX infusions were prospectively registered from both the eHealth and the control groups.
Full Information
NCT ID
NCT01860651
First Posted
May 20, 2013
Last Updated
February 13, 2019
Sponsor
Hvidovre University Hospital
Collaborators
University of Copenhagen
1. Study Identification
Unique Protocol Identification Number
NCT01860651
Brief Title
Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease
Official Title
Patient Empowerment: Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease for Better Quality of Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
May 2017 (Actual)
Study Completion Date
May 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital
Collaborators
University of Copenhagen
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators hypothesize that E-health - web based monitoring of disease and treatment - in young patients with chronic inflammatory disease (IBD) can improve the disease course and quality of life.
Adherence (to take the prescribed medicine) is difficult for young patients. In this E-health project the investigators seek to improve young patients (10-17 years) responsibility for treatment, to empower them and thereby enhance the adherence in order to achieve a more quiet disease course. Through the e-Health program and web-app the disease activity will be presented to the young patient via a simple traffic light chart and the patient will be guided to: continue the prescribed medication, call the physician or visit the out-patient clinic. In future the concept is believed also to be applicable for young patients with other chronic diseases.
Detailed Description
IBD's natural history is characterized by relapses (e.g. rectal bleeding, diarrhoea, abdominal pain, faecal urgency, fistula and anal abscess) and remissions. In children and adolescents the disease has a more aggressive course as compared with adults, causing a deterioration in the quality of life. During puberty patients are in an especially vulnerable period of their lives and there is a high risk for developing social disabilities due to the disease. Furthermore, IBD can lead to many days of absence from school and patients are at risk of not being able to maintain their education.
Patients are treated medically when the disease is active, but also in quiet phases too in order to maintain remission. It is therefore crucial for success that patients receive insight into the disease and understand the importance of following the recommended maintenance treatment. Despite being aware of an increased risk of acute hospitalization and surgery, it is difficult for both adult and pediatric patients to follow the continuous medication (adherence). It is known that up to 50% of young patients fail to take their medication as directed.
Previous studies have used E-health in the treatment of IBD patient. In M. Elkjaer et al. 2010 study on 300 patients with mild-to-moderate UC, E-health treatment resulted in shorter periods of active disease (average 18 vs. 77 days in the control group), 88% were satisfied with their treatment using E-health and the need for outpatient visits was reduced. In another study, Pedersen et al. 2012, on 27 patients with CD and examining biological treatment, E-Health was able to optimize the timing of infliximab treatment in CD patients. The E-Health solution was safe to use and patients showed high adherence to the program (86%). To the investigators knowledge no study has previously used E-health treatment in children and adolescents with IBD. It is, however, the investigators belief that this treatment concept would be readily taken up such patients, for whom web communication, at least in Denmark, is already a well-integrated part of their daily lives.
The current study consists of two projects: Project A: Patients in treatment with medicine administrated at home. Project B: Patients in treatment with biological infusions
Project A: Patients in treatment with medicine administrated at home are monitored, according to current international guidelines, with outpatient visits every third month. Patients participating in the current project will be randomly split into two groups and followed for two years. E-health group: Web-monitoring with an annual visit to the IBD center. Control group: Routine outpatient controls, four times a year.
Project B: According to current guidelines, patients receiving treatment with biologicals visit the outpatient clinic approximately every eighth week and treatment is given intravenously. During the E-health intervention, symptoms and fecal calprotectin are monitored closely through the web-program, and treatment will be initiated by symptoms and elevated FC. In this way the timing of treatment with biologicals can be optimized and infusions delayed with a maximum treatment-free period of 12 weeks, or earlier than 8 weeks if necessary.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease, Ulcerative Colitis, Crohn´s Disease
Keywords
Inflammatory Bowel Disease, Ulcerative Colitis, Crohn´s Disease, Children, Adolescence, E-health web-monitoring, Adherence, Disease activity, Fecal Calprotectin
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
103 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Web-monitoring
Arm Type
Active Comparator
Arm Description
There is two arms for intervention:
1) Patients in treatment with medicine administrated at home and 2) patients in treatment with biologicals.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients in treatment with medicine administrated at home: routine outpatient controls, four times a year.
Patients in treatment with biologicals: retrospective routine treatment algorithm
Intervention Type
Behavioral
Intervention Name(s)
Web-monitoring
Intervention Description
During the E-health intervention, symptoms and FC are monitored closely through the web-program and treatment will be initiated by symptoms and elevated FC.
Primary Outcome Measure Information:
Title
Medical Adherence
Description
Participants (group 1, medication adm. at home): Medicine Adherence Report Scale (MARS): range 5-25 points. Higher scores mean a better outcome. In the below Outcome Measure Data Table the mean data for each group (web and control) summarized from the whole study periode are presented.
Time Frame
Prospective, each third month, up to 2 years
Secondary Outcome Measure Information:
Title
Number of Participants With Step up in Medical Intensity
Description
Time to frist step-up in treatment intensity (escalating dose or change/addition of a more potent drug) were obtained from the patient's medical record during the study period, as a proxy of progression in disease activity.
Time to step up was analysed via Kaplan Meier survival analysis.
Time Frame
The first event during participation (2 years). (events were prospecitvely registered)
Title
Surgery
Description
Need for surgery
Time Frame
The first event during participation (2 years). (events were prospecitvely registered)
Title
Absence From School
Description
Number of days absence from school
Time Frame
Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years
Title
Contact to the Hospital
Description
Need for outpatient visits
Time Frame
Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years
Title
Number of Weeks Between Treatment
Description
Date of IFX infusions were prospectively registered from both the eHealth and the control groups.
Time Frame
Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
IBD diagnosis according to the Copenhagen and Porto criteria
Aged between 10-17 years
Fluent in Danish
Access to the internet
Patients in treatment with infliximab must have completed the induction period (i.e. minimum six week after start-up of treatment).
Exclusion Criteria:
Insufficient Danish language skills
Lack of intellectual capacity
Growth retardation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katrine Carlsen, MD
Organizational Affiliation
Department of Pediatrics, Hvidovre Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vibeke Wewer, MD, PhD
Organizational Affiliation
Department of Pediatrics, Hvidovre Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Pia Munkholm, Professor
Organizational Affiliation
Department of Gastroenterology, Herlev Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Christian Jakobsen, MD, PhD
Organizational Affiliation
Department of Pediatrics, Hvidovre Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lene Riis, MD, PhD
Organizational Affiliation
Department of Pathology, Herlev Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Pediatrics, Hvidovre Hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
28169974
Citation
Carlsen K, Jakobsen C, Kallemose T, Paerregaard A, Riis LB, Munkholm P, Wewer V. F-calprotectin and Blood Markers Correlate to Quality of Life in Pediatric Inflammatory Bowel Disease. J Pediatr Gastroenterol Nutr. 2017 Nov;65(5):539-545. doi: 10.1097/MPG.0000000000001540.
Results Reference
derived
Learn more about this trial
Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease
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