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Telemedical, Intersectoral Network as New Digital Health Structure to Measurably Improve the Local Health Care

Telemedical, Intersectoral Network as New Digital Health Structure to Measurably Improve the Local Health Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03137589
Acronym
TELnet@NRW
Enrollment
159065
Registered
2017-05-03
Start date
2017-05-01
Completion date
2020-01-31
Last updated
2020-06-02

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

Conditions

Infection, Intensive Care Patients

Keywords

Telemedicine

Brief summary

Telemedicine allows providing expert know-ledge from specialized health centers to regional hospitals and practices. In this multicenter, prospective, non-interventional study hospitals and practices in NRW are supplied via a telematics platform with expertise from the university hospitals RWTH Aachen and Münster. The communication occurs via highly encrypted audio/video conference systems and a certified data exchange platform Fallakte+. In total 40.000 outpatient and stationary patients with infectious diseases or need for intensive care should be treated with telemedical support. The participating hospitals and practices are randomly distributed into four clusters. The clusters are supplied with telemedicine at different time points but all clusters start at the same time collecting data from patient cohorts of infectiology and intensive care (e.g. symptom, therapeutic progress and outcome). The collected data is later compared to data obtained in the same way from patients treated with telemedical support and evaluated regarding differences in the quality of treatment, therapeutic process and the satisfaction of the patients with telemedicine. The aim is to improve the treatment quality in regional hospitals and practices of patients with serious and complex diseases and bring forward the application of telemedicine.

Detailed description

In future time the number of old people will significantly increase in Germany because of the demographic change taking place. The health care of the large number of old people will probably lead to a lack of physicians and an inefficient health care system. One strategy to tackle the problem could be telemedicine. Telemedicine makes it possible to provide know-ledge from experts to local hospitals and practices which otherwise need to send patients with serious and complex diseases to specialized trans-regional health centers. In this multicenter, prospective, non-interventional study hospitals and practices in NRW are supplied via a telematics platform with expert know-ledge from the university hospitals RWTH Aachen and Münster. The communication occurs via highly encrypted audio/video conference systems and a certified data exchange platform Fallakte+. In total 40.000 outpatient and stationary patients should be treated with telemedical support. Registered doctors will be involved in already existing practice networks to evaluate the potential for transfer and to ensure the sharing of know-ledge beyond the borders of individual sectors. The aim of the study is to improve the treatment quality of regional hospitals and practices and to increase the efficiency of the care of relevant patient cohort in the field of infectiology and intensive care with the main focus sepsis as those patient groups especially often require professional expertise for a successful therapy. In the beginning of the study participating hospitals and practices are randomly distributed into four clusters (cluster randomization). The different clusters all start with the control phase but enter into the intervention phase at different times (stepped-wedge design). During the control phase data of patients with infection and intensive care patients routinely treated without the support of telemedicine are documented and the patients are asked to complete a questionnaire regarding health-related quality of life (SF36) directly after treatment and at two time points in the follow-up. The collected data will be later compared to data obtained in the same way from patients treated with telemedical support and evaluated regarding differences in the quality of treatment, therapeutic process and the satisfaction of the patients with telemedicine. If the study shows that the treatment quality and therapeutic process of patients with infectious diseases or need for intensive care is improved by telemedicine, the telematics platform can be expanded and used by other specialized fields and users in future time.

Interventions

Participating sites will be advised by telemedicine support.

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Stepped-Wedge-Design

Eligibility

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

Inclusion criteria

* majority * written informed consent * infectiological and/or intensive care treatment

Exclusion criteria

* minority * absence of written informed consent in the case of non-acute life-threatening disease * persons who have a dependency or employment relationship with the sponsor or investigator * persons who are sheltered in an institution upon court or administrative order

Design outcomes

Primary

MeasureTime frameDescription
Improvement of treatment qualitythrough study completion, an average of 30 days up to a maximum of 1 yearThe level of implementation of the 10 recommendations of the German Society of Infectious Diseases (Deutsche Gesellschaft für Infektiologie, DGI) within the framework of the Initiative Decide wisely (Klug entscheiden).

Secondary

MeasureTime frameDescription
Rate of ARDS Diagnosisthrough study completion, an average of 30 days up to a maximum of 1 yearRate of ARDS Diagnosis
Sepsis therapy in compliance with guidelinesthrough study completion, an average of 30 days up to a maximum of 1 yearSepsis therapy in compliance with guidelines through for instance timely administration of antibiotics within 3 h and reduction of sepsis mortality.
Rate of ARDS therapy according to guidelinesthrough study completion, an average of 30 days up to a maximum of 1 yearMeasured against the evident ventilation targets, Ventilation with low ventilation volumes and low peak pressures: with controlled ventilation: Breath volume of 6 ml/kg calculated Body ideal weight, PEEP setting in proportion with the necessary FiO2, plateau pressure \< 30 cm H2O
Rate of inadequate antibiotic therapiesthrough study completion, an average of 30 days up to a maximum of 1 yearMeasured by the Percentage of postoperatively continued perioperative Antibiotic prophylaxis
Rate of patients with dialysisAt discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 yearRate of patients with dialysis requiring Kidney insufficiency in discharge from the Intensive care
Rate of transfer transportAt discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 yearRate of transfer transport
Rate of sepsis diagnosisthrough study completion, an average of 30 days up to a maximum of 1 yearRate of sepsis diagnosis
Rate of non-diagnosed sepsisthrough study completion, an average of 30 days up to a maximum of 1 yearDefined as no filled out sepsis bundle despite presence of sepsis symptoms
Sepsis mortality ratethrough study completion, an average of 30 days up to a maximum of 1 yearSepsis mortality rate
Hospital mortality ratethrough study completion, an average of 30 days up to a maximum of 1 yearHospital mortality rate
Length of stay in intensive care unitAt discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 yearLength of stay in intensive care unit measured in hours
Hospital stayAt discharge from Hospital; after an average of 30 days up to a maximum of 1 yearHospital stay measured in days
Health-related quality of life (SF36-Questionnaire)At discharge from Intensive Care Unit (through study completion; an average of 30 days up to a maximum of 1 year), through study completion, an average of 12 months and 24 months after discharge of ICUClinical studies 36-item Medical Outcomes Study Short-Form General Health Survey An instrument used to assess multidimensional health-related QOL, which measures 8 health related parameters: physical function, social function, physical role, emotional role, mental health, energy, pain, general health perceptions; each parameter is scored from 0 to 100 Managed care 36-Item Short-Form Functional and Perceived Health Status Survey A questionnaire which measures health status; the SF-36 also includes a list of 18 self-reported chronic conditions

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026