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Clinical Trials/NCT01860651
NCT01860651CompletedNot Applicable

Patient Empowerment: Web-based Monitoring in Children and Adolescents With Inflammatory Bowel Disease for Better Quality of Treatment

Hvidovre University Hospital1 site in 1 country103 target enrollmentStarted: September 1, 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
103
Locations
1
Primary Endpoint
Medical Adherence

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
10 Years to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Web-monitoring

Active Comparator

There is two arms for intervention:

  1. Patients in treatment with medicine administrated at home and 2) patients in treatment with biologicals.

Intervention: Web-monitoring (Behavioral)

Control

No Intervention

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 Outcomes

Medical Adherence

Time Frame: Prospective, each third month, up to 2 years

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 Outcomes

  • Number of Weeks Between Treatment(Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years)
  • Absence From School(Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years)
  • Contact to the Hospital(Prospective, each third month, - disease activity each month(project A) or week(project B), in 2 years)
  • Number of Participants With Step up in Medical Intensity(The first event during participation (2 years). (events were prospecitvely registered))
  • Surgery(The first event during participation (2 years). (events were prospecitvely registered))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Katrine Carlsen, MD

MD

Hvidovre University Hospital

Study Sites (1)

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