跳至主要内容
临床试验/DRKS00021507
DRKS00021507已完成4 期

A randomized, controlled, investigator-blinded, multicenter, single-cross-over interventional pilot study to investigate the effect of virtual reality enhanced education on rheumatoid arthritis for healthcare professionals on knowledge, illness perception and empathy toward patients with rheumatoid arthritis: the VENTURE trial - VENTURE-Trial

Justus Liebig Universität Gießen, Campus Kerckhoff, Abt. für Rheumatologie, Immunologie, Osteologie und Physikalische Medizin0 个研究点目标入组 40 人开始时间: 2020年8月25日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Healthcare Professional working in Rheumatology

排除标准

  • Key Exclusion Criteria. Please see study protocol for a complete list.
  • - a diagnosis of a rheumatic disease
  • - neurologic disease prohibiting the use of virtual reality
  • - any disease prohiniting the use of virtual reality

研究者

发起方
Justus Liebig Universität Gießen, Campus Kerckhoff, Abt. für Rheumatologie, Immunologie, Osteologie und Physikalische Medizin

相似试验

进行中(未招募)
不适用
An randomized, controlled, investigator-blinded, prospective, mono-centre study to evaluate the efficacy of fosfomycin versus meropenem in patients with complicated urinary tract infections - urosepsis/fosfo vs. meropenemThis study will primarily address the question of the efficacy of intravenous fosfomycin 4 g b.i.d. in the therapy of patients presenting with complicated urinary tract infection. These data will be compared to meropenem administered intravenously at a dose of 2 g b.i.d.MedDRA version: 9.1Level: LLTClassification code 10046571Term: Urinary tract infection
EUCTR2007-005112-37-ATMedizinische Universität Wien, Abteilung für Interne Medizin I240
进行中(未招募)
1 期
Study of safety, tolerability, pharmacokinetics and pharmacodynamics of QBW251 in subjects with bronchiectasisMedDRA version: 23.0Level: LLTClassification code 10083611Term: Non-cystic fibrosis bronchiectasisSystem Organ Class: 100000004855Bronchiectasis
EUCTR2019-002840-26-GBovartis Pharma AG72
进行中(未招募)
1 期
Study of LIK066 in overweight and obese women with polycystic ovary syndromepolycystic ovary syndromeMedDRA version: 20.0Level: LLTClassification code 10036050Term: Polycystic ovarySystem Organ Class: 100000004872
EUCTR2017-001373-16-DEovartis Pharma AG29
进行中(未招募)
1 期
Study of safety, tolerability, pharmacokinetics and pharmacodynamics of QBW251 in subjects with bronchiectasisMedDRA version: 23.0Level: LLTClassification code 10083611Term: Non-cystic fibrosis bronchiectasisSystem Organ Class: 100000004855Bronchiectasis
EUCTR2019-002840-26-DEovartis Pharma AG72
进行中(未招募)
1 期
Study to assess the efficacy and safety of CJM112 in patients with inadequately controlled severe asthmaInadequately controlled moderate to severe asthmaMedDRA version: 20.0 Level: PT Classification code 10003553 Term: Asthma System Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
EUCTR2017-000205-21-DKovartis Pharma AG110