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Telemedical, Intersectoral Network as New Digital Health Structure to Measurably Improve the Local Health Care (TELnet@NRW)

2020년 6월 1일 업데이트: RWTH Aachen University
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.

연구 개요

상태

완전한

상세 설명

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.

연구 유형

중재적

등록 (실제)

159065

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Münster, 독일
        • University Hospital Münster
    • NRW
      • Aachen, NRW, 독일, 52074
        • University Hospital RWTH Aachen

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 특수 증상
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
간섭 없음: Control
Patients of this group are routinely treated without telemedical support.
활성 비교기: Telemedical support
Patients of this group are routinely treated with telemedical support.
Participating sites will be advised by telemedicine support.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Improvement of treatment quality
기간: through study completion, an average of 30 days up to a maximum of 1 year
The 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").
through study completion, an average of 30 days up to a maximum of 1 year

2차 결과 측정

결과 측정
측정값 설명
기간
Rate of sepsis diagnosis
기간: through study completion, an average of 30 days up to a maximum of 1 year
Rate of sepsis diagnosis
through study completion, an average of 30 days up to a maximum of 1 year
Rate of ARDS Diagnosis
기간: through study completion, an average of 30 days up to a maximum of 1 year
Rate of ARDS Diagnosis
through study completion, an average of 30 days up to a maximum of 1 year
Sepsis therapy in compliance with guidelines
기간: through study completion, an average of 30 days up to a maximum of 1 year
Sepsis therapy in compliance with guidelines through for instance timely administration of antibiotics within 3 h and reduction of sepsis mortality.
through study completion, an average of 30 days up to a maximum of 1 year
Rate of ARDS therapy according to guidelines
기간: through study completion, an average of 30 days up to a maximum of 1 year

Measured 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

through study completion, an average of 30 days up to a maximum of 1 year
Rate of inadequate antibiotic therapies
기간: through study completion, an average of 30 days up to a maximum of 1 year
Measured by the Percentage of postoperatively continued perioperative Antibiotic prophylaxis
through study completion, an average of 30 days up to a maximum of 1 year
Rate of patients with dialysis
기간: At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Rate of patients with dialysis requiring Kidney insufficiency in discharge from the Intensive care
At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Rate of transfer transport
기간: At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Rate of transfer transport
At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Health-related quality of life (SF36-Questionnaire)
기간: 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 ICU
Clinical 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
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 ICU
Rate of non-diagnosed sepsis
기간: through study completion, an average of 30 days up to a maximum of 1 year
Defined as no filled out sepsis bundle despite presence of sepsis symptoms
through study completion, an average of 30 days up to a maximum of 1 year
Sepsis mortality rate
기간: through study completion, an average of 30 days up to a maximum of 1 year
Sepsis mortality rate
through study completion, an average of 30 days up to a maximum of 1 year
Hospital mortality rate
기간: through study completion, an average of 30 days up to a maximum of 1 year
Hospital mortality rate
through study completion, an average of 30 days up to a maximum of 1 year
Length of stay in intensive care unit
기간: At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Length of stay in intensive care unit measured in hours
At discharge from Intensive Care Unit (study completion); after an average of 30 days up to a maximum of 1 year
Hospital stay
기간: At discharge from Hospital; after an average of 30 days up to a maximum of 1 year
Hospital stay measured in days
At discharge from Hospital; after an average of 30 days up to a maximum of 1 year

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Gernot Marx, Univ.-Prof. Dr. med., Clinic for Operative Intensive Care and Intermediate Care, University Hospital RWTH Aachen

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2017년 5월 1일

기본 완료 (실제)

2019년 10월 31일

연구 완료 (실제)

2020년 1월 31일

연구 등록 날짜

최초 제출

2017년 4월 28일

QC 기준을 충족하는 최초 제출

2017년 4월 28일

처음 게시됨 (실제)

2017년 5월 3일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2020년 6월 2일

QC 기준을 충족하는 마지막 업데이트 제출

2020년 6월 1일

마지막으로 확인됨

2020년 1월 1일

추가 정보

이 연구와 관련된 용어

키워드

기타 연구 ID 번호

  • 16-162

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

Telemedical support에 대한 임상 시험

구독하다