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Liver CirrhosismyLiverCOACHNCT07376967

Improving Healthcare Outcomes With Early Detection of Liver Related Complications in Liver Cirrhosis Patients by Implementing a Telemedicine Care Pathway (myLIVERcoach)

A study testing telemedicine pathway in people with Liver Cirrhosis, run by Maastricht University at 2 sites in Netherlands.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this multicenter feasibility study is to investigate the feasibility of our telemedicine platform (myLIVERcoach) in liver cirrhosis patients, according to liver cirrhosis patients, caregivers and healthcare professionals. The main question[s] it aims to answer are: 1. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Liver Cirrhosis
What is being tested?
telemedicine pathway
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
2 sitesNetherlands
Study dates
1 May 2023to 1 May 2025
Phase
Interventional
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 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients ≥ 18 years of age or caregiver of a patient (both ≥ 18 years of age)
  • Liver cirrhosis, based on biopsy, fibroscan or diagnostic imaging data or caregiver of a patient with this diagnosis

Who cannot join

  • Inability to read or understand informed consent
  • Lack of internet access
  • History of or current hepatocellular carcinoma
  • History of or current hepatic metastasis
  • History of liver transplantation

Trial locations and contacts

2 sites in 1 country.

Netherlands2 sites
  • Gelre Ziekenhuizen

    Apeldoorn, Gelderland, 7334 DZ

  • Maastricht University Medical Center

    Maastricht, Limburg, 6202 AZ

Other trials in Netherlands

About this study

Official title: Improving Healthcare Outcomes With Early Detection of Liver Related Complications in Liver Cirrhosis Patients by Implementing a Telemedicine Care Pathway (myLIVERcoach): a Multicenter Feasibility Study

The goal of this multicenter feasibility study is to investigate the feasibility of our telemedicine platform (myLIVERcoach) in liver cirrhosis patients, according to liver cirrhosis patients, caregivers and healthcare professionals. The main question[s] it aims to answer are:

  1. What is the feasibility of a telemonitoring pathway according to patients, caregivers and healthcare professionals in liver cirrhosis care? Secondary objectives:
  2. What is the level of acceptability, usability, learnability and desirability of a telemonitoring pathway in liver cirrhosis care from the patients, caregivers and healthcare professionals' perspective?
  3. What is the level of compliance of patients, caregivers and healthcare professionals using a telemonitoring pathway in liver cirrhosis care?
  4. What is the occurrence of liver related complications in liver cirrhosis patients using a telemonitoring pathway?
  5. What is the occurrence of clinical admissions and emergency concultations in liver cirrhosis patients using a telemonitoring pathway?
  6. What is the mortality rate in liver cirrhosis patients using a telemonitoring pathway?
  7. What is the effect of a telemonitoring pathway on patients perceived health, quality of life and work participation of liver cirrhosis patients?
Read more

Participants will be asked to use myLIVERcoach on top of standard care. According to disease stadium participants will receive different online questionnaires and measurements, focusing on early detection of complications and psychosocial and lifestyle factors. Participants are able to contact their healthcare professional and go through information about their disease as well.

After six months, participants will be asked to fill out a questionnaire regarding their experiences with myLIVERcoach in order to optimize the system. In addition the investigators will perform interviews with ten patients or caregivers and with healthcare professionals at the end of follow-up.

Read the detailed description

Methods Study parameters/endpoints Main study parameter/endpoint Feasibility of this telemonitoring pathway in liver cirrhosis patients will be defined by results of the acceptability questionnaire, appendix B.

A score of ≥4.0 in ≥70% of patients, caregivers and healthcare professionals together will be defined as feasible.

Results of the question ''I would recommend the application to others'', see appendix B. A score ≥4.0 in ≥70% of patients, caregivers and healthcare professionals together is defined as significant satisfaction, one of the main aspects of adequate feasibility.

Feasibility will be evaluated in the interviews as well. The telemonitoring pathway will be defined feasible if ≥70% of interviewed patients and at least three (out of five) healthcare professionals find the telemonitoring of value in the domains: acceptance of implementation in standard liver cirrhosis care, support of self-management and adequate technological functioning.

Secondary study parameters

  1. Compliance is divided into responsiveness to questionnaires and e-learnings and completion of questionnaires and e-learnings.
  2. Adequate compliance regarding responsiveness is defined as ≥70% of patients and caregivers starting the provided questionnaires and e-learnings.
  3. Adequate compliance regarding completion is defined as ≥70% of patients and caregivers completing the provided questionnaires and e-learnings.
  4. Usability, learnability, and desirability are defined as a mean score of ≥4.0 in ≥70% patients, caregivers, and healthcare professionals together.
  5. Occurrence of liver related complications (ascites, hepatic encephalopathy, and variceal bleeding) will be described using percentage of occurred complication and how many times patients developed this complication.
  6. Occurrence of clinical admissions will be described using percentage of occurred clinical admissions and how often patients were admitted.
  7. Emergency consultations will be described using percentage of occurred emergency consultation and how many times patients had those consultations.
  8. Mortality will be described using percentage of occurred death.
  9. Perceived health will be monitored before and after follow-up and the investigators will investigate significant differences in disease status within patients before and after using the telemonitoring pathway.
  10. Quality of life will be monitored before and after follow-up and the investigators will investigate significant differences in quality of life within patients before and after using the telemonitoring pathway.
  11. Work participation will be monitored before and after follow-up and the investigators will investigate significant differences in work participation within patients before and after using the telemonitoring pathway.
  12. Social functioning will be monitored before and after follow-up and the investigators will investigate significant differences in social functioning within patients before and after using the telemonitoring pathway.
  13. Adequate detection of complications will be classified as ≥70% of complication specific exceeding thresholds in myLIVERcoach leading to change in treatment
  14. Adequate comprehensibility of the liver complication specific questionnaire according to patients, caregivers and healthcare professionals will be classified as ≥70% acknowledgement during the interviews of understanding all the individual questions.

Data collection Research data from myLIVERcoach will be coded, encrypted, and stored in repositories of Datahub Maastricht, a so called trusted third party. Data conducted from the electronic patient files will be stored in Castor. Every participating hospital will manage research data of their specific patients. Key documents, to which just the principal investigator and coordinating researcher have access, will be saved separately in the participating hospitals.

Patients and caregivers During a study period of 6 months, patients will fill in questionnaires in myLIVERcoach regarding disease specific complaints, quality of life and subjective wellbeing in intervals according to the group participants are subjected to (compensated, non-actively decompensated and actively decompensated). Participants will complete separate questionnaires regarding satisfaction with current healthcare and acceptability of the telemonitoring pathway at baseline and at 6 months. Caregivers will fill in questionnaires regarding current healthcare for the patient and will be asked to complete the myLIVERcoach questionnaires together with the patient. The investigators will evaluate different aspects with ten to twenty patients using the telemonitoring pathway in a semi-structured 30-60-minute interview.

The investigators can measure patients and caregivers' compliance to the modules and questionnaires of the telemonitoring pathway in terms of starting a module, completing it and duration until completion. The investigators will search electronic patient files to investigate occurrence of liver related complications, clinical admissions, emergency consultations and mortality.

Healthcare professionals During 6 months, healthcare professionals are able to monitor patients' responses to questions and e-learnings and receive alarm signals in case of exceeding thresholds. Participants will complete separate questionnaires regarding satisfaction acceptability of the telemonitoring pathway at baseline and at 6 months. The investigators will evaluate different aspects including compliance with at least 5 healthcare professionals in a semi-structured 30-60-minute interview.

Design and content development The backbone of the technical system and general content of our telemonitoring system is based on myIBDcoach. This is a well-tested and validated digital platform that supports the healthcare provider in monitoring, guiding, educating, and communicating with patients diagnosed with inflammatory bowel diseases (IBD) [17]. The investigators were able to use approximately 60% of the general content in myIBDcoach. Decisions regarding which general and liver-specific content should be included in our telemonitoring pathway were made in brainstorm sessions of our content committee. The content committee included a representative from the Dutch Liver Patient Association (NLV), a hospital pharmacist, 4 gastroenterologists/hepatologists (academic/non-academic and including an electronic Health expert), a dietician, 2 specialized hepatology nurses, a physical therapist and a clinical researcher who is responsible for continuation, development and contact with the software provider. In the 2 months prior to start of the feasibility study our content committee has iteratively tested and reviewed our telemonitoring pathway after which it has been improved and tested again until it was found worthy for patient use in the feasibility study. See fig. 1.

Conditions
Liver Cirrhosis
Being tested
telemedicine pathway
Keywords
Telemedicine, eHealth, Telemonitoring, mobile health
Medical subject headings
Liver Cirrhosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • telemedicine pathwayDevice

    Patients are able to use an online application on top of standard care. Monitoring complications, subjective wellbeing and lifestyle factors. Patients are able to go through information about liver cirrhosis and additional aspects, like dietary advices, at any moment in time. Furthermore, they are able to contact their healthcare professional through the chat function.

Study groups in NCT07376967
Study groupRoleWhat they receive
Patients using telemedicine on top of standard careOtherNot described
Receives: Device: telemedicine pathway

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Feasibility defined by the number of recommendations to use this telemonitoring pathway by patients, caregivers and healthcare profesionals.

    A score of ≥4.0 in ≥70% of patients, caregivers and healthcare professionals together will be defined as feasible.

    Using a likert scale, minimum value 1 (worst), maximum value 5 (best) Results of the question ''I would recommend the application to others'', see appendix B. A score ≥4.0 in ≥70% of patients, caregivers and healthcare professionals together is defined as significant satisfaction, one of the main aspects of adequate feasibility.

    Measured: 6 months

Secondary outcomes (9)
  1. Compliance defined by ≥70% initiated questionnaires and e-learnings of actual provided questionnaires and e-learnings.

    Using a percentage based upond the number of provided questionnaires and the number of questionnaires actually initiated by patients and caregivers.

    Measured: 6 months

  2. Compliance defined by ≥70% completed questionnaires and e-learnings of actual provided questionnaires and e-learnings.

    Using a percentage based upond the number of provided questionnaires and the number of questionnaires actually completely finished by patients and caregivers.

    Measured: 6 months

  3. Usability defined as a mean score of ≥4.0 in ≥70% patients, caregivers, and healthcare professionals together in the question ''It was easy to indicate my complaints with myLIVERcoach.''

    Using a likert scale, minimum value 1 (worst), maximum value 5 (best)

    Measured: 6 months

  4. Learnability defined as a mean score of ≥4.0 in ≥70% patients, caregivers, and healthcare professionals together in the question ''It was easy to learn how I had to use myLIVERcoach''.

    Using a likert scale, minimum value 1 (worst), maximum value 5 (best)

    Measured: 6 months

  5. Desirability defined as a mean score of ≥4.0 in ≥70% patients, caregivers, and healthcare professionals togethe in the question ''MyLIVERcoach meets my approval.''

    Using a likert scale, minimum value 1 (worst), maximum value 5 (best)

    Measured: 6 months

  6. Number of liver related complications

    Measured: 6 months

  7. Clinical admissions

    Occurrence of clinical admissions will be described using percentage of occurred clinical admissions and how often patients were admitted.

    Measured: 6 months

  8. Emergency consultations

    Emergency consultations will be described using percentage of occurred emergency consultation and how many times patients had those consultations.

    Measured: 6 months

  9. Mortaility

    Mortality will be described using percentage of occurred death.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jan 2026
  2. Study start1 May 2023
  3. Primary completion1 May 2025
  4. Study completion1 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07376967
Sponsor's protocol ID
METC 2022-3567
Acronym
myLiverCOACH
Status last verified
Sep 2025
First submitted
23 May 2023
Last updated
29 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing telemedicine pathway in people with Liver Cirrhosis, run by Maastricht University at 2 sites in Netherlands.

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 2 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: finished, as of the sponsor's last update on 29 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Netherlands. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Feasibility defined by the number of recommendations to use this telemonitoring pathway by patients, caregivers and healthcare profesionals. (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 29 Jan 2026.

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