Inflammatory Bowel DiseasesNCT03604536
Individualization Treatment Through a Self-managed Web-based Solution in Ulcerative Colitis
An observational study of Inflammatory Bowel Diseases and Ulcerative Colitis, run by Nordsjaellands Hospital at 1 site in Denmark.
Trial summary
This study investigates the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission in patients with mild to moderate UC in an eHealth setting. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Inflammatory Bowel Diseases, Ulcerative Colitis
- How many people
- 1 participants
- Where
- 1 siteDenmark
- Study dates
- 2 Dec 2019to 31 Dec 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: 20 patients with mild to moderate ulcerative colitis will be included from the Out patient clinic at the gastroenterology department, North Zealand University Hospital, Capitol region of Denmark
Who may be able to join
- Fulfil the Copenhagen Diagnostic criteria for UC
- Age between 18 and 75 years
- New and relapse patients diagnosed with Mild-to-moderate UC
- Current relapse (minimum 1 out of 2) SCCAI>2 (with a positive score in the variable of blood in stool) FC ≥200
- Diagnosed with left sided or extensive UC(24)
- Understand written and spoken Danish
- Easy access to internet and smartphone
Who cannot join
- Evidence of enteric infection
- Treatment with immunomodulators such as steroids, azathioprine, methotrexate, or infliximab within the last 8 weeks
- Two or more courses of oral steroids in the past 12 months
- Diagnosed with proctitis
- Severe disease activity (SCCAI >6 or FC ≥600)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Individualization of Oral Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis: A Pilot Study
This study investigates the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission in patients with mild to moderate UC in an eHealth setting.
Read the detailed description
More than 3 million Europeans suffer from inflammatory bowel disease (IBD), where Crohn's Disease (CD) and Ulcerative Colitis (UC) are the most common forms. They are chronic, relapsing and remitting diseases resulting in uncontrolled inflammation of the gastrointestinal (GI) tract with symptoms of diarrhoea, abdominal pain, weight loss and blood in the stools. The treatment aims to relieve and prevent GI tract inflammation and consists of anti-inflammatory and immunosuppressive drugs or surgical removal of the colon as a final option. The main treatment option for mild to moderate UC is Aminosalicylate. Mesalazine (5-aminosalicylic acid), both orally and topically, has been proven to be an effective treatment option for inducing as well as maintaining remission in patients with UC.
Pentasa Sachet are Mesalazine micro granules coated in ethyl cellulose with high (95%) 5-aminosalicylic acid (5-ASA) load. The coating provides a prolonged release of Mesalazine, allowing a continuous action from small bowel to rectum. Approximately 75% of the micro granules are released in the colon. This reduces the number of applications needed per day and is therefore considered to be a more desirable option by the patients. Once daily administrated 5-aminosalicylic acid (5-ASA) has been shown to be as effective as conventional dosing.
Fecal Calprotectin (FC) is an accurate biomarker of GI tract inflammation. FC correlates well with endoscopic disease activity and consequently serves as a substitute marker for mucosal healing as well as a clinical tool for disease monitoring. A home testing kit with a smart phone application, which only takes 18 min to carry out, has been developed. Thereby, facilitating the opportunity of telemonitoring of the disease course and stimulating patient engagement, empowerment and adherence to treatment.
Medication adherence is essential for maintaining remission, since non-adherence is one of the main causes of disease activity. A combined therapy of oral and topical 5-ASA is recommended by current guidelines for the treatment of active mild to moderate UC. However, patient adherence to oral 5-ASA is poor (approximately 60%), and even poorer to topical therapy (approximately 32%). A previous eHealth trial on individualized oral 5-ASA therapy reported higher adherence rates than previous studies on standard care. In addition, 90% of the study patients responded with remission on monotherapy and only 10% needed a combined therapy with topical treatment.
Web-based treating solutions (eHealth) have shown to optimize treatment effect in chronic diseases such as asthma, type 1 diabetes, and coagulation diseases. A web-based treatment solution for IBD patients, Constant-care, was in 1997 launched by Dr. Pia Munkholm. The web-program has since been proven to be an effective clinical tool, resulting in enhanced compliance, empowerment, improved quality of life and decreased relapse duration in IBD patients. Constant-Care consists of an education package and a disease-monitoring package. The disease monitoring part of the program is built upon an algorithm of two variables; FC and a validated disease activity questionnaire, Simple Clinical Colitis Activity Index (SCCAI) for UC patients. The FC values are acquired by the patients through a home testing kit and the disease activity questionnaire is filled out by the patients in the web- program. The eHealth system cumulates the data immediately, and subsequently presenting the result, a Total inflammatory Burden Score (TIBS), to the patients as a visual "traffic light" indicator of disease activity. Patients receive treatment advices by the program depending on the severity of the disease: green- remission, yellow- moderate activity, red-severe activity.
The disease monitoring part also consists of Patient-Related Outcome (PRO) questionnaires regarding quality of life, disability, fatigue, disease course type and compliance. The International Organization for the study of Inflammatory Bowel Disease (IOIBD) has since 2015 recommended the use of PRO's as a fundamental part of measuring treatment outcome in both UC and CD.
The primary aim of the study is to investigate the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission (clinical and Paraclinical (green TIBS)) in patients with mild to moderate UC in an eHealth setting. The investigators hypothesize that the web based therapy program will reduce the time to remission compared to standard care.
- Conditions
- Inflammatory Bowel Diseases, Ulcerative Colitis
- Keywords
- Adherence, eHealth, Aminosalicylate
- Medical subject headings
- Inflammatory Bowel Diseases, Colitis, Ulcerative
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Total Inflammation Burden Scoring (TIBS)
Self reported disease activity in combination with a fecal biomarker of inflammation (fecal calprotectin) results in TIBS. Disease activity is scored by 6 questions yielding: remission (<3) , mild to moderate disease activity (3-4) and severe disease activity ( >5). Fecal calprotectin: remission (<200mg/kg ), mild to moderate (200-599 mg/kg ), severe (>599 mg/kg). The two items are added together in a weighted manner giving the Total inflammation burden scoring (TIBS): remission (0-8), mild to moderate (9-32), severe (33-99).
Measured: At baseline and at 12 weeks or until remission, which ever comes first
Secondary outcomes (5)
Disease course type
Self reported Disease course type according to the Copenhagen disease course type ( 5 different types). The five disease course types stretch from mild and indolent to constant active disease. In this study, patients have to choose one type representing their disease course since time of diagnosis, as well as at week 12 for the period since inclusion in the study.
Measured: At baseline and after 12 weeks
Compliance with medication
self reported according to the Medicine Adherence Report Scale and visibility analog scale. Compliance scored according to Medicine Adherence Report Scale by 5 questions, and 1-5 points per question ( 5 = always, 1=never), maximum score 25. A score over 20 is considered god compliance.
Visibility analog scale from 0-100, where 0 means no compliance and 100 means 100% compliant.
Measured: at baseline and after 12 weeks
Short Inflammatory Bowel Disease Questionnaire
self reported quality of life according to the Short Inflammatory Bowel Disease Questionnaire, a disease specific health related quality of life questionnaire consisting of 10 questions in four domains: Emotional Health, Bowel Symptoms, Social Health and Work. The scoring range is from 10 (lowest score) to 70 (highest score). A cut-off level at >50 is interpreted as good health related quality of life.
Measured: at baseline and after 12 weeks
Disability
self reported disability according to the IBD disk, consisting of 10 items: Abdominal pain, regulating defecation, interpersonal interactions, education and work, Sleep, energy, emotions, body image, sexual functions, joint pain. Patients can score from 0 (absolutely disagree/ no disability) to 10 (absolutely agree/severe disability) for each item. The results will be visualised to the patient as a coloured disc.
Measured: at baseline and after 12 weeks
Fatigue
Fatigue is measured according to The Functional Assessment of Chronic Illness Therapy-Fatigue Scale, containing 13 questions to measure the fatigue component of health related quality of life. The scale ranges from 0-52 with zero being the worst possible score and 52 the best. A score of ≤30 represents fatigue
Measured: at baseline and after 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jul 2018
- Study start2 Dec 2019
- Primary completion31 Aug 2021
- Study completion31 Dec 2021
Why it stopped: not able to recruit patients
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Inflammatory Bowel DiseasesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1 participants (actual)
Sponsor and investigators
- Lead sponsor
- Nordsjaellands Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Ferring Pharmaceuticals
- Responsible party
- Principal investigator, Petra Weimers, Nordsjaellands Hospital
- Investigators
- Pia Munkholm, Prof, Study director, North Zealand University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03604536
- Sponsor's protocol ID
- H-17038710
- Status last verified
- Feb 2022
- First submitted
- 9 Jul 2018
- Last updated
- 9 Mar 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Vinding KK, Elsberg H, Thorkilgaard T, Belard E, Pedersen N, Elkjaer M, Marker D, Carlsen K, Burisch J, Munkholm P. Fecal Calprotectin Measured By Patients at Home Using Smartphones--A New Clinical Tool in Monitoring Patients with Inflammatory Bowel Disease. Inflamm Bowel Dis. 2016 Feb;22(2):336-44. doi: 10.1097/MIB.0000000000000619.
PubMed 26535869Pedersen N, Thielsen P, Martinsen L, Bennedsen M, Haaber A, Langholz E, Vegh Z, Duricova D, Jess T, Bell S, Burisch J, Munkholm P. eHealth: individualization of mesalazine treatment through a self-managed web-based solution in mild-to-moderate ulcerative colitis. Inflamm Bowel Dis. 2014 Dec;20(12):2276-85. doi: 10.1097/MIB.0000000000000199.
PubMed 25248002Elkjaer M, Shuhaibar M, Burisch J, Bailey Y, Scherfig H, Laugesen B, Avnstrom S, Langholz E, O'Morain C, Lynge E, Munkholm P. E-health empowers patients with ulcerative colitis: a randomised controlled trial of the web-guided 'Constant-care' approach. Gut. 2010 Dec;59(12):1652-61. doi: 10.1136/gut.2010.220160.
PubMed 21071584Pedersen N, Elkjaer M, Duricova D, Burisch J, Dobrzanski C, Andersen NN, Jess T, Bendtsen F, Langholz E, Leotta S, Knudsen T, Thorsgaard N, Munkholm P. eHealth: individualisation of infliximab treatment and disease course via a self-managed web-based solution in Crohn's disease. Aliment Pharmacol Ther. 2012 Nov;36(9):840-9. doi: 10.1111/apt.12043.
PubMed 22971016
Study at a glance
From the registry record, last updated by the sponsor on 9 Mar 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Individualization of Oral Mesalazine Treatment Through a Self-managed Web-based Solution in Mild-to-moderate Ulcerative Colitis: A Pilot Study
- ClinicalTrials.gov ID
- NCT03604536
- Acronym / sponsor ID
- H-17038710
- Conditions
- Inflammatory Bowel Diseases, Ulcerative Colitis
- Keywords
- Adherence, eHealth, Aminosalicylate
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: not able to recruit patients
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Nordsjaellands HospitalUniversity, hospital or other
- Collaborators
- Ferring Pharmaceuticals
- Study start
- 2 Dec 2019 (actual)
- Primary completion
- 31 Aug 2021 (actual)
- Study completion
- 31 Dec 2021 (actual)
- First posted
- 27 Jul 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study investigates the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission in patients with mild to moderate UC in an eHealth setting.
Detailed description
More than 3 million Europeans suffer from inflammatory bowel disease (IBD), where Crohn's Disease (CD) and Ulcerative Colitis (UC) are the most common forms. They are chronic, relapsing and remitting diseases resulting in uncontrolled inflammation of the gastrointestinal (GI) tract with symptoms of diarrhoea, abdominal pain, weight loss and blood in the stools. The treatment aims to relieve and prevent GI tract inflammation and consists of anti-inflammatory and immunosuppressive drugs or surgical removal of the colon as a final option. The main treatment option for mild to moderate UC is Aminosalicylate. Mesalazine (5-aminosalicylic acid), both orally and topically, has been proven to be an effective treatment option for inducing as well as maintaining remission in patients with UC.
Pentasa Sachet are Mesalazine micro granules coated in ethyl cellulose with high (95%) 5-aminosalicylic acid (5-ASA) load. The coating provides a prolonged release of Mesalazine, allowing a continuous action from small bowel to rectum. Approximately 75% of the micro granules are released in the colon. This reduces the number of applications needed per day and is therefore considered to be a more desirable option by the patients. Once daily administrated 5-aminosalicylic acid (5-ASA) has been shown to be as effective as conventional dosing.
Fecal Calprotectin (FC) is an accurate biomarker of GI tract inflammation. FC correlates well with endoscopic disease activity and consequently serves as a substitute marker for mucosal healing as well as a clinical tool for disease monitoring. A home testing kit with a smart phone application, which only takes 18 min to carry out, has been developed. Thereby, facilitating the opportunity of telemonitoring of the disease course and stimulating patient engagement, empowerment and adherence to treatment.
Medication adherence is essential for maintaining remission, since non-adherence is one of the main causes of disease activity. A combined therapy of oral and topical 5-ASA is recommended by current guidelines for the treatment of active mild to moderate UC. However, patient adherence to oral 5-ASA is poor (approximately 60%), and even poorer to topical therapy (approximately 32%). A previous eHealth trial on individualized oral 5-ASA therapy reported higher adherence rates than previous studies on standard care. In addition, 90% of the study patients responded with remission on monotherapy and only 10% needed a combined therapy with topical treatment.
Web-based treating solutions (eHealth) have shown to optimize treatment effect in chronic diseases such as asthma, type 1 diabetes, and coagulation diseases. A web-based treatment solution for IBD patients, Constant-care, was in 1997 launched by Dr. Pia Munkholm. The web-program has since been proven to be an effective clinical tool, resulting in enhanced compliance, empowerment, improved quality of life and decreased relapse duration in IBD patients. Constant-Care consists of an education package and a disease-monitoring package. The disease monitoring part of the program is built upon an algorithm of two variables; FC and a validated disease activity questionnaire, Simple Clinical Colitis Activity Index (SCCAI) for UC patients. The FC values are acquired by the patients through a home testing kit and the disease activity questionnaire is filled out by the patients in the web- program. The eHealth system cumulates the data immediately, and subsequently presenting the result, a Total inflammatory Burden Score (TIBS), to the patients as a visual "traffic light" indicator of disease activity. Patients receive treatment advices by the program depending on the severity of the disease: green- remission, yellow- moderate activity, red-severe activity.
The disease monitoring part also consists of Patient-Related Outcome (PRO) questionnaires regarding quality of life, disability, fatigue, disease course type and compliance. The International Organization for the study of Inflammatory Bowel Disease (IOIBD) has since 2015 recommended the use of PRO's as a fundamental part of measuring treatment outcome in both UC and CD.
The primary aim of the study is to investigate the effect of individualized monotherapy with Mesalazine (Pentasa Sachet ®) on time to remission (clinical and Paraclinical (green TIBS)) in patients with mild to moderate UC in an eHealth setting. The investigators hypothesize that the web based therapy program will reduce the time to remission compared to standard care.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- 20 patients with mild to moderate ulcerative colitis will be included from the Out patient clinic at the gastroenterology department, North Zealand University Hospital, Capitol region of Denmark
Key inclusion criteria (7 listed)
- Fulfil the Copenhagen Diagnostic criteria for UC
- Age between 18 and 75 years
- New and relapse patients diagnosed with Mild-to-moderate UC
- Current relapse (minimum 1 out of 2) SCCAI>2 (with a positive score in the variable of blood in stool) FC ≥200
- Diagnosed with left sided or extensive UC(24)
Key exclusion criteria (5 listed)
- Evidence of enteric infection
- Treatment with immunomodulators such as steroids, azathioprine, methotrexate, or infliximab within the last 8 weeks
- Two or more courses of oral steroids in the past 12 months
- Diagnosed with proctitis
- Severe disease activity (SCCAI >6 or FC ≥600)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Change in Total Inflammation Burden Scoring (TIBS)
Time frame: At baseline and at 12 weeks or until remission, which ever comes first
Self reported disease activity in combination with a fecal biomarker of inflammation (fecal calprotectin) results in TIBS. Disease activity is scored by 6 questions yielding: remission (<3) , mild to moderate disease activity (3-4) and severe disease activity ( >5). Fecal calprotectin: remission (<200mg/kg ), mild to moderate (200-599 mg/kg ), severe (>599 mg/kg). The two items are added together in a weighted manner giving the Total inflammation burden scoring (TIBS): remission (0-8), mild to moderate (9-32), severe (33-99).
5 secondary outcomes
Disease course type
Time frame: At baseline and after 12 weeks
Compliance with medication
Time frame: at baseline and after 12 weeks
Short Inflammatory Bowel Disease Questionnaire
Time frame: at baseline and after 12 weeks
Disability
Time frame: at baseline and after 12 weeks
Fatigue
Time frame: at baseline and after 12 weeks
Results and safety
The study was stopped early (reason given: not able to recruit patients). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Mar 2022.
- Background: PubMed 26535869Vinding KK, Elsberg H, Thorkilgaard T, Belard E, Pedersen N, Elkjaer M, Marker D, Carlsen K, Burisch J, Munkholm P. Fecal Calprotectin Measured By Patients at Home Using Smartphones--A New Clinical Tool in Monitoring Patients with Inflammatory Bowel Disease. Inflamm Bowel Dis. 2016 Feb;22(2):336-44. doi: 10.1097/MIB.0000000000000619.
- Background: PubMed 25248002Pedersen N, Thielsen P, Martinsen L, Bennedsen M, Haaber A, Langholz E, Vegh Z, Duricova D, Jess T, Bell S, Burisch J, Munkholm P. eHealth: individualization of mesalazine treatment through a self-managed web-based solution in mild-to-moderate ulcerative colitis. Inflamm Bowel Dis. 2014 Dec;20(12):2276-85. doi: 10.1097/MIB.0000000000000199.
- Background: PubMed 21071584Elkjaer M, Shuhaibar M, Burisch J, Bailey Y, Scherfig H, Laugesen B, Avnstrom S, Langholz E, O'Morain C, Lynge E, Munkholm P. E-health empowers patients with ulcerative colitis: a randomised controlled trial of the web-guided 'Constant-care' approach. Gut. 2010 Dec;59(12):1652-61. doi: 10.1136/gut.2010.220160.
- Background: PubMed 22971016Pedersen N, Elkjaer M, Duricova D, Burisch J, Dobrzanski C, Andersen NN, Jess T, Bendtsen F, Langholz E, Leotta S, Knudsen T, Thorsgaard N, Munkholm P. eHealth: individualisation of infliximab treatment and disease course via a self-managed web-based solution in Crohn's disease. Aliment Pharmacol Ther. 2012 Nov;36(9):840-9. doi: 10.1111/apt.12043.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pia Munkholm, Prof study director
North Zealand University Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Inflammatory Bowel Diseases and Ulcerative Colitis, run by Nordsjaellands Hospital at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 9 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: not able to recruit patients). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Total Inflammation Burden Scoring (TIBS) (time frame: At baseline and at 12 weeks or until remission, which ever comes first). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03604536, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Mar 2022.