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The Effect of MedicijnWijs on Adherence to Azathioprine Therapy in Adolescents With IBD (MEDICATION)

Primary Purpose

Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
MedicijnWijs
Sponsored by
Maxima Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Inflammatory Bowel Diseases focused on measuring Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis, Adherence, Azathioprine, Knowledge, App, Phone, Education

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 12 up to and including 17 years old
  • Condition: IBD (Crohn's Disease and Ulcerative Colitis)
  • Treatment: azathioprine

Exclusion Criteria:

- Inability to use MedicijnWijs due to either low cognitive skills or the unavailability of a phone or other technical device to use the app on

Sites / Locations

  • Catharina Hospital
  • Zuyderland Medisch Centrum
  • Maxima Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MedicijnWijs

Arm Description

All participants will undergo the same intervention of using MedicijnWijs, and they will serve as their own control.

Outcomes

Primary Outcome Measures

Change in adherence to azathioprine therapy
Measured as the change in Medication Adherence Report Scale-5 (MARS-5) score compared to baseline. The MARS-5 score at the start and end of the study can range from 5 to 25 points. The higher the score, the better the adherence to azathioprine therapy. The difference in MARS-5 score compared to baseline will be assessed.

Secondary Outcome Measures

Change in knowledge about IBD
Measured as the change in Inflammatory Bowel Disease-Knowledge Inventory Device 2 (IBD-KID2) score compared to baseline. The IBD-KID2 score at the start and end of the study can range from 0 to 15 points. The higher the score, the higher the knowledge about IBD. The difference in IBD-KID2 score compared to baseline will be assessed.
Ease of use of MedicijnWijs assessed by a questionnaire
Assessed by separate questions

Full Information

First Posted
March 23, 2022
Last Updated
April 4, 2022
Sponsor
Maxima Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05321485
Brief Title
The Effect of MedicijnWijs on Adherence to Azathioprine Therapy in Adolescents With IBD
Acronym
MEDICATION
Official Title
The Effect of MedicijnWijs on Adherence to Azathioprine Therapy in Adolescents With IBD
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 16, 2022 (Actual)
Primary Completion Date
September 16, 2022 (Anticipated)
Study Completion Date
September 16, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Maxima Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Medication non-adherence is an existing problem in patients with inflammatory bowel diseases (IBD). Adherence rates are especially low in children and adolescents. Good medication adherence is key in achieving lower disease activity and longer periods of remission. Previous research has shown education can increase medication adherence. MedicijnWijs is a mobile phone app containing a module concerning a 6-weeks guidance with azathioprine therapy. It provides information about IBD and azathioprine. In this multicenter before-and-after study, the aim is to assess the effect of MedicijnWijs on the adherence to azathioprine therapy in adolescents with IBD. This is done using two validated questionnaires that are translated to Dutch: the Medication Adherence Report Scale-5 (MARS-5), which tests the participants' adherence to azathioprine therapy, and the Inflammatory Bowel Disease Knowledge Inventory Device 2 (IBD-KID2), which tests the participants' knowledge about IBD. These questionnaires are filled in at the beginning of the study period and after 6 weeks of using MedicijnWijs. This way a change in both scores can be assessed. The investigators hypothesize that MedicijnWijs will help increase the adherence to azathioprine therapy in adolescents with IBD.
Detailed Description
Rationale: medication non-adherence is an existing problem in patients with inflammatory bowel diseases (IBD). Adherence rates are especially low in children and adolescents. Good medication adherence is key in achieving lower disease activity and longer periods of remission. Previous research has shown education can increase medication adherence. MedicijnWijs is a mobile phone app containing a module concerning a 6-weeks guidance with azathioprine therapy. The aim of this study is to assess the effect of MedicijnWijs on the adherence to azathioprine therapy in adolescents with IBD. The investigators hypothesize that MedicijnWijs will help increase the adherence to azathioprine therapy in adolescents with IBD. Objective: with this study, the effect of the mobile phone app MedicijnWijs on adherence to azathioprine therapy will be assessed. In addition, the effect on knowledge about IBD and the ease of use of MedicijnWijs will be studied as well. Study design: this study is a multicenter before-and-after study. Study population: the study population are adolescents aged 12 up to and including 17 years old. All participants are diagnosed with IBD and are treated with azathioprine. This multicenter study will be conducted in Máxima Medical Center in Veldhoven, Catharina Hospital in Eindhoven, and Zuyderland Medical Center in Sittard-Geleen/Heerlen, The Netherlands. Intervention: the participants will use the mobile phone app MedicijnWijs for 6 weeks. In this app, information about IBD and azathioprine is provided. Participants also receive questions about their symptoms through the app. Moreover, at the beginning of the study the participants have to fill in two validated questionnaires that are translated to Dutch in the app: the Medication Adherence Report Scale-5 (MARS-5), which tests the participants' adherence to azathioprine therapy, and the Inflammatory Bowel Disease Knowledge Inventory Device 2 (IBD-KID2), which tests the participants' knowledge about IBD. After 6 weeks, the participants have to fill out the same questionnaires again to assess potential changes in the scores compared to baseline. Also, a number of questions will be asked to assess the ease of use of MedicijnWijs. Main study parameters/endpoints: the main endpoint is change in adherence to azathioprine therapy measured as a change in MARS-5 score. In addition, the secondary endpoint change in knowledge about IBD measured as a change in IBD-KID2 score will be studied as well. The results of the secondary endpoint ease of use of MedicijnWijs will be presented descriptively. Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: there are no risks associated with participation to this study as participants only have to use a mobile phone app and fill in two short questionnaires. MedicijnWijs has to be used for 6 weeks. The time burden per day varies from 0 to 10 minutes. The IBD treatment of the participants will not change, and participants will visit their doctors as frequently as usual. Only an additional introductory talk will be necessary, which will be scheduled during a regular outpatient clinic visit. No physical examinations, blood tests, or other tests will be done during this study apart from routine care of IBD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis
Keywords
Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis, Adherence, Azathioprine, Knowledge, App, Phone, Education

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MedicijnWijs
Arm Type
Experimental
Arm Description
All participants will undergo the same intervention of using MedicijnWijs, and they will serve as their own control.
Intervention Type
Other
Intervention Name(s)
MedicijnWijs
Intervention Description
The mobile phone app MedicijnWijs will guide the participants with their azathioprine therapy during 6 weeks. Information about azathioprine is given as well as general information about IBD, specified to disease modality (Crohn's Disease and Ulcerative Colitis). Contact details of the patient's pharmacy are listed, questions about the patient's symptoms are asked, and push notifications are added to remind the patients to take their medication. At the beginning of the 6-weeks guidance, two validated questionnaires that are translated and validated in Dutch will have to be filled in: the MARS-5 and the IBD-KID2. After 6 weeks, the participants have to fill out the same questionnaires again to assess potential changes in the scores compared to baseline. Also, a number of questions will be asked to assess the ease of use of MedicijnWijs.
Primary Outcome Measure Information:
Title
Change in adherence to azathioprine therapy
Description
Measured as the change in Medication Adherence Report Scale-5 (MARS-5) score compared to baseline. The MARS-5 score at the start and end of the study can range from 5 to 25 points. The higher the score, the better the adherence to azathioprine therapy. The difference in MARS-5 score compared to baseline will be assessed.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Change in knowledge about IBD
Description
Measured as the change in Inflammatory Bowel Disease-Knowledge Inventory Device 2 (IBD-KID2) score compared to baseline. The IBD-KID2 score at the start and end of the study can range from 0 to 15 points. The higher the score, the higher the knowledge about IBD. The difference in IBD-KID2 score compared to baseline will be assessed.
Time Frame
6 weeks
Title
Ease of use of MedicijnWijs assessed by a questionnaire
Description
Assessed by separate questions
Time Frame
At the end of 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 12 up to and including 17 years old Condition: IBD (Crohn's Disease and Ulcerative Colitis) Treatment: azathioprine Exclusion Criteria: - Inability to use MedicijnWijs due to either low cognitive skills or the unavailability of a phone or other technical device to use the app on
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kaylee Stabel, BSc
Phone
+31629161384
Email
kaylee.stabel@mmc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Luc JJ Derijks, PharmD, PhD
Email
l.derijks@mmc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luc JJ Derijks, PharmD, PhD
Organizational Affiliation
Maxima Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Catharina Hospital
City
Eindhoven
State/Province
Noord-Brabant
ZIP/Postal Code
5623EJ
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Janneke M Stapelbroek, MD, PhD
Email
janneke.stapelbroek@catharinaziekenhuis.nl
First Name & Middle Initial & Last Name & Degree
Inge GPT Sauvé-van Gorp
First Name & Middle Initial & Last Name & Degree
Janneke M Stapelbroek, MD, PhD
First Name & Middle Initial & Last Name & Degree
Inge GPT Sauvé-van Gorp
Facility Name
Zuyderland Medisch Centrum
City
Heerlen
State/Province
Noord-Brabant
ZIP/Postal Code
6419PC
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nanja Bevers, MD
Email
n.bevers@zuyderland.nl
First Name & Middle Initial & Last Name & Degree
Nanja Bevers, MD
Facility Name
Maxima Medical Center
City
Veldhoven
State/Province
Noord-Brabant
ZIP/Postal Code
5500VB
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kaylee Stabel, BSc
Phone
+31629161384
Email
kaylee.stabel@mmc.nl
First Name & Middle Initial & Last Name & Degree
Luc JJ Derijks, PharmD, PhD
Email
l.derijks@mmc.nl
First Name & Middle Initial & Last Name & Degree
Luc JJ Derijks, PharmD, PhD
First Name & Middle Initial & Last Name & Degree
Kaylee Stabel, BSc
First Name & Middle Initial & Last Name & Degree
Coby Mesman, MSc
First Name & Middle Initial & Last Name & Degree
Imke A Bertrams-Maartens, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Effect of MedicijnWijs on Adherence to Azathioprine Therapy in Adolescents With IBD

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