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Clinical Trials in Denmark / NCT07166653
Recruiting Not applicable

Hospital-at-Home Education as Implementation Tool - RCT

NCT07166653 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2025-09-10

Condition(s) studied

Hospital

Investigational drug(s) / intervention(s)

HaH education

HaH education: The intervention consists of the online NorDigHE HaH education with tailored implementation tools em-bedded in the WHO Fast-IM. The education is delivered online and asynchronously, combining e-learning, simulations, reflection exercises, and practical task training. The trial has adopted the evidence-based WHO Fast-track Implementation Model (WHO Fast-IM) as a framework to support the effectiveness and reporting of the implementation, and the tailored implementation tools embedded in the model will be provided as part of the intervention to support in-tegration into daily clinical routines. The tailored toolbox consists of workshops, introductory meetings, written guides, and access to a hotline staffed by project specialists to facilitate implementation.

Study summary

To enhance implementation of Hospital-at-home (HaH) in Scandinavia, the Nordic Digital Health \& Education (NorDigHE) project has developed a comprehensive virtual education on HaH for clinical staff. The goal of this clinical trial is to evaluate whether an online education for clinical staff can enhance the implementation of HaH services in hospitals across Denmark, Norway, and Sweden.

The primary outcome of the RCT is HaH implementation measured at organization level, understood as a change in clinical practice by increased HaH activity. Secondary outcomes are HaH knowledge and motivation among clinical staff as well as patient days in hospital, days hospitalized at home, 30-day readmission, and mortality.

Researchers will compare hospitals receiving the NorDigHE education (intervention group) to hospitals continuing treatment as usual (control group) to see if the education leads to greater adoption of HaH and changes in service delivery.

Participants will:

* Complete baseline, 3-month, and 6-month surveys assessing HaH activity, staff knowledge, and motivation.
* Participate in a 12-month follow-up assessment (intervention group only).
* Be invited (patients, staff, and management) to take part in semi-structured interviews to share experiences and preferences related to HaH.
* (For staff in the intervention group) Complete the NorDigHE virtual education program embedded in the WHO Fast-IM.

After the study, the control group will be offered access to the NorDigHE education as a participant retention measure.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion criteria: Hospitals with clinical departments treating acutely ill in-patients that have, or are ready to establish, the prerequisites and infrastructure for HaH - regardless of the specific approach, envisioned HaH model, primary sector collaborations, or local sector collaboration agreements and frameworks. Each hospital must have or be ready to establish: 1. a governance structure to organize and oversee HaH-services. 2. an IT-platform capable of managing data from and to HaH patients. 3. a safe communication pathway between HaH-patient and the hospital. 4. clear agreements on types of data to be exchanged between HaH-patient and hospital. 5. agreements on roles, responsibilities, and capacity (incl. possibly primary sector entities). 6. clinical guidelines, standard operating procedures, and action plans to support the HaH work. Exclusion Criteria: * Hospitals that do not have or are not ready to secure relevant pre-requisites listed above (a to f).

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Nordsjællands Hospital Hillerød Capitol Region of Denmark Recruiting
University College of Østfold Fredrikstad Østfold fylke Recruiting
Sahlgrenska University hospital Göteborg Skåne County Recruiting

More Nordsjaellands Hospital trials in Denmark

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07166653 on ClinicalTrials.gov ↗ ← All trials in Denmark