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IBD Self-management Website and Home Faecal Calprotectin Monitoring

Feasibility and Acceptability of an Inflammatory Bowel Disease Self-management Website and Home Faecal Calprotectin Monitoring After Treatment De-escalation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03671980
Enrollment
11
Registered
2018-09-14
Start date
2017-04-04
Completion date
2018-06-30
Last updated
2018-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn Disease, Inflammatory Bowel Diseases, Self-care, Ulcerative Colitis

Keywords

Calprotectin

Brief summary

6 month exploratory feasibility study to assess if a combination of MyMedicalRecord supported self-management website and a home faecal calprotectin smartphone testing kit is a feasible and acceptable means for patients to monitor for signs of relapse after treatment de-escalation.

Detailed description

IBD can be challenging to manage as disease flares are often unpredictable and rarely coincide with scheduled outpatient appointments. Websites are a novel way of assisting patients to take more control over monitoring and managing symptoms and have been shown to improve outcomes in some chronic diseases. The My Medical Record (MyMR) webiste was developed to help patients learn about IBD, access test results, monitor symptoms, and manage their medications, with email support from the IBD team. The use of home faecal calprotectin monitoring will also be explored. This marker of IBD activity is normally performed in hospital laboratories and becomes elevated before the onset of clinical symptoms of an IBD flare. New technologies enable patients to perform the test at home with the aid of a smartphone application. A 6 month exploratory feasibility study will be conducted to assess if a combination of MyMR and a home faecal testing kit is a feasible and acceptable means for patients to monitor their illness. Their use will be targeted to patients who have recently stopped (or reduced) a treatment for IBD, as up to 50% of these patients may have a disease flare within a year. Interventions * Clinic appointments Study participants will not be required to attend any routine outpatient follow up appointments for the 6 month study period, after which they will be reviewed by a member of the IBD team. * Questionnaires and interviews Partcipants will receive questionnaires and a sample will also undergo interviews to explore their views regarding the website and stool test. * Website Participants will be encouraged to use all functions of the website at least monthly: 1. Secure email messaging service 2. IBD educational material 3. Stool, nutritional and flare journals 4. Blood and test results 5. Faecal calprotectin monitoring - monthly testing (or sooner if symptoms of a flare-up) using QuantonCal home faecal calprotectin smartphone application. Participants will test and monitor their FC levels monthly. The results will be overseen by the IBD team who will make contact within a week in the event of abnormal results if the participant has not already done so. * Blood tests All participants will have a routine blood test at 0 and 6 months. Those taking azathioprine, mercaptopurine and methotrexate should continue regular blood monitoring (minimum of 3 monthly FBC, U&E, LFT and CRP) as usual practice. Participants will be provided with blood test results and explanations of their significance via MyMR. The results will be overseen by the IBD team who will make contact within a week in the event of abnormal results if the patient has not already done so. * Safety Patients can contact the IBD team the email messaging service at any time for advice and support.

Interventions

OTHERMy Medical record website

Website comprising patient records, blood and other test results, useful information on IBD, and messaging service to communicate with IBD team, plus home smartphone faecal calprotectin monitoring.

Sponsors

University of Southampton
CollaboratorOTHER
University Hospital Southampton NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Feasibility study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged ≥ 18 years currently under secondary care outpatient follow up for IBD * Diagnosed with IBD at least one year prior to study enrolment (to ensure patients are familiar with their disease and treatments) * Stopped or reduced the dose of one or more treatments for IBD (for any reason) within the last 8 weeks * Able to understand English and provide written consent. * Own, or have regular (at least weekly) access to a smartphone +/- personal computer with internet

Exclusion criteria

* Inability to read, understand informed consent * Inability to use a smartphone * Likely requirement of IBD surgery within the study period * Ileostomy * Pregnancy or planned pregnancy within next 6 months * Terminal illness with limited (\< 1year) life expectancy * Current participation in another IBD research study * Any reason, in the opinion of the investigators, which is likely to make the patient unsuitable for the study

Design outcomes

Primary

MeasureTime frameDescription
Faecal calprotectin testing completion rates6 monthsNumber of patients completing monthly faecal calprotectin testing
MyMR website usage6 monthsNumber of patients logging in to MyMR website at least monthly

Secondary

MeasureTime frameDescription
IBD flareline calls6 monthsNumber of IBD flareline telephone calls per patient to IBD specialist nursing team
IT support contact6 monthsNumber of IT support email contacts per patient
Questionnaire response rates6 monthsResponse rates to pre-and post-study questionnaires
Retention rate6 monthsStudy retention rate (target 80%). Study retention will be defined as successful completion of at least 5 out of 7 home faecal calprotectin tests, with no periods without login to website of greater than 3 consecutive months.
Recruitment6 monthsNumber of patients recruited per month
IBD-Control6 monthsMean IBD-Control scores at 0, 4, 8, 12, 16, 20, and 24 weeks
SIBDQ6 monthsMean quality of life (SIBDQ) scores at 0 and 26 weeks
IBD knowledge6 monthsMean IBD knowledge scores (CC-KNOW) at 0 and 26 weeks.
Calprotectin levels6 monthsMean faecal calprotectin levels at 0, 4, 8, 12, 16, 20, and 24 weeks.
IBD email contact6 monthsNumber of email messaging contacts per patient to IBD specialist nursing team

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026