ClinicalTrials.gg
RecruitingNCT07010081Updated Oct 1, 2025

Using Digital Health in a Postoperative Setting After Major Surgery: Survey Study

An interventional study of Surveys in Digital Health, sponsored by Jessa Hospital. Recruiting at 1 site in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-10-01.

Sponsored by Jessa Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
220
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This study aims to explore patients' use of digital services for self-management of their health following major surgery at Jessa Hospital. Besides this, the study evaluates patients' ability to process and critically assess health information during recovery, their understanding of health concepts and risk factors, and their perception of data security and control over personal health information. Additionally, the study aims to examine patients' motivation to use digital services, their access to and trust in reliable digital health resources, and how well these services meet their individual needs. Furthermore, the study assesses the acceptability, appropriateness, and feasibility of using digital health tools in a post-operative setting, as well as evaluating the digital readiness of patients after surgery.

Read the detailed description

Digital health technologies are transforming healthcare, offering new ways to improve patient outcomes and enhance efficiency. Remote clinical monitoring (RCM), which uses digital technologies such as wearable devices and mobile apps to monitor patients outside of the traditional healthcare settings such as a hospital, holds significant potential for supporting post-operative care, especially in the context of faster hospital discharge after major surgery. Major surgery involves procedures on organ systems, such as cancer resections, organ transplants, and lung or abdominal surgeries. However, despite their promise, the successful implementation of these technologies into clinical practice requires a thorough understanding of the perspectives of the end user, being the patient. Patients' comfort, engagement, and perceptions about digital health solutions, such as self-management tools and remote monitoring pathways, are essential to ensuring these technologies are both effective and widely accepted.

02

Conditions studied

  • Digital Health

Keywords

  • Remote monitoring
  • Major surgery
03

In context

Lead sponsor

Jessa Hospital is the lead sponsor of 85 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Surgical patients

    • >18 years old, Undergone major surgery at Jessa Hospital Hasselt

Exclusion criteria

Exclusion Criteria:

  • Unable to provide or request to not participate in the study
  • Cognitively incapable of understanding the study
  • No understanding of the Dutch language
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
220 participants (estimated)

Study arms

  • Experimental
    Surveys

    Conducting questionnaires during a follow-up consultation after major surgery

    Procedure: Surveys

Interventions

  • ProcedureSurveys

    Several questionnaires will be conducted once in-person to each patient after a follow-up consultation in the hospital after their major surgery

06

What researchers measure

Primary outcomes

  1. Patients' understanding of comfort and engagement with using digital services for self- management of their disease

    The patients' understanding of comfort and engagement with using digital services for self- management of their disease after major surgery will be evaluated using scale 4 of the eHLQ.

    Time frame: During a follow-up consultation within one year after major surgery

Secondary outcomes

  1. Ability of patients to use technology to process and critically evaluate health information

    The ability of patients to use technology to process and critically evaluate health information during postoperative recovery will be evaluated using scale 1 of the eHLQ.

    Time frame: During a follow-up consultation within one year after major surgery

  2. Patients' understanding of health concepts, their health status, and risk factors

    Scale 2 of the eHLQ will assess patients' understanding of health concepts, their health status, and risk factors during their recovery period.

    Time frame: During a follow-up consultation within one year after major surgery

  3. Patients' perception of data security and control over personal health data

    To assess patients' perception of data security and control over personal health data in digital services, scale 4 of the eHLQ will be used.

    Time frame: During a follow-up consultation within one year after major surgery

  4. Patients' motivation to use digital services for managing postoperative health

    Scale 5 of the eHLQ is used to examine patients' motivation to use digital services for managing their postoperative health.

    Time frame: During a follow-up consultation within one year after major surgery

  5. Patients' access to and trust in reliable digital health services

    The sixth scale of the eHLQ will evaluate patients' access to and trust in reliable digital health services during recovery.

    Time frame: During a follow-up consultation within one year after major surgery

  6. The extent to which digital health services meet patients' individual needs and preferences

    To assess how well digital health services meet patients' individual needs and preferences during recovery, scale 7 of the eHLQ will be used.

    Time frame: During a follow-up consultation within one year after major surgery

  7. Acceptability, appropriateness, and feasibility of using digital health by means of implementation outcome measures AIM, IAM, and FIM

    To evaluate the acceptability, appropriateness, and feasibility of using digital health in a postoperative setting after major surgery, the AIM, IAM, and FIM, respectively, will be used.

    Time frame: During a follow-up consultation within one year after major surgery

  8. Digital readiness

    The DHRQ will be used to assess digital readiness of patients that underwent major surgery.

    Time frame: During a follow-up consultation within one year after major surgery

  9. External validation of the digital health readiness questionnaire

    The DHRQ will be externally validated against the extensively validated eHLQ.

    Time frame: During a follow-up consultation within one year after major surgery

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07010081
Lead sponsor
Jessa Hospital
Responsible party
Stessel Björn (Professor, Dr, Jessa Hospital) — Principal investigator
First posted
Jun 8, 2025
Start date
May 26, 2025
Primary completion
May 1, 2026 (estimated)
Completion
May 1, 2027 (estimated)
Last update
Oct 1, 2025

Study contacts

Bjorn Stessel, MD, PhD
Contact
bjorn.stessel@jessazh.be
+3211222107

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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