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Telemedicine clinical trials

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NCT ID: NCT03007745 Completed - Telemedicine Clinical Trials

Remote Sleep Apnea Management

Start date: October 24, 2017
Phase: N/A
Study type: Interventional

Although obstructive sleep apnea, a breathing disorder during sleep, is prevalent and recognized as a major public health concern, most Veterans with this disorder are undiagnosed and therefore untreated. Access to sleep laboratories for testing is limited particularly for those Veterans living in rural areas and Veterans with disabilities that prevent travel to a sleep center. The goal of this study is to compare a web-based telehealth management strategy to in-person management. The telehealth pathway will enable Veterans to be diagnosed and treated without visiting a sleep center. The investigators believe that telehealth management will increase Veterans' access to this specialized care at a cost that is less than in-person delivery but with similar improvements in daytime function.

NCT ID: NCT03004716 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Telemonitoring in Pulmonary Rehabilitation: Validity of a Remote Pulse Oxymetry System

TELE-REHAB
Start date: January 2017
Phase: N/A
Study type: Observational

The purpose of this study is to assess the feasibility and the reliability of a telemonitoring system during pulmonary rehabilitation in patients with chronicle obstructive pulmonary disease. The feasibility is assessed using the patient's satisfaction and it ease of use. The reliability of the remote telemonitoring system is assessed comparing the local data (extracted from the monitoring device itself) and the data transmitted through the telemonitoring platform.

NCT ID: NCT02956395 Completed - Chronic Disease Clinical Trials

Implementation of Community-based Collaborative Management of Complex Chronic Patients

Nextcare_CCP
Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Background/Aims: Large scale adoption of integrated care for chronic patients constitutes a key milestone to accelerate adaptation of current healthcare systems to the evolving needs triggered by population ageing and high prevalence of chronic conditions. Lessons learnt from deployment experiences are being disseminated as "good practices". But, there is need for further assessment of implementation strategies in real world scenarios. Moreover, progresses achieved in disease-oriented integrated care cannot be automatically transferred to management of complex chronic patients (CCP). The protocol addresses five aims: 1) implementation of two integrated care interventions using a collaborative and adaptive case management (ACM) approach (i) Community-based management of CCP; and, ii) Integrated care for patients under long-term oxygen therapy (LTOT)); 2) adoption of information and communication technologies (ICT) required to support collaborative ACM; 3) to evaluate the impact of enhanced clinical health risk assessment and stratification; 5) to generate a roadmap for regional adoption of the CCP program. Methods/Design: the CCP program will be deployed in three healthcare sector of Barcelona-Esquerra (AISBE) (520 k citizens) and in two other areas of Catalonia: Badalona Serveis Assistencials (BSA) (420 k citizens) and Lleida (366 k citizens) following Plan-Do-Study-Act iterative cycles, using the Model for Assessment of Telemedicine for evaluation purposes. The study also addresses the steps for scale-up of integrated care in the entire Catalan region (7.5 M citizens). Observational studies with matched controls have been planned for both Community-based management of CCP (n=3.000) and for Integrated care for patients under LTOT (n=500). Moreover, clustered randomized controlled trials (RCT) are planned on top of the observational studies to test specific questions (i.e. performance of the ICT platform providing ACM functionalities). Main components of CCP program are: a) patient stratification; b) comprehensive assessment strategies; c) ICT supported adaptive Case management; d) Roadmap for regional adoption. Hypothesis: the CCP program will generate guidelines for large scale deployment of the CCP program, including transferability analysis, facilitating adoption of integrated care services for management of multi-morbidity.

NCT ID: NCT02928705 Completed - Analgesia Clinical Trials

Quality of Telemedically Guided Prehospital Analgesia

Start date: January 2014
Phase: N/A
Study type: Observational

The purpose of this retrospective study is to analyze quality and adverse events of analgesia by telemedically supported paramedics in comparison to conventional treatment by on-scene emergency medical service (EMS) physicians in the EMS of the city of Aachen, Germany.

NCT ID: NCT02779894 Completed - Clinical trials for Obstructive Sleep Apnea

Sleep Apnoea Management by a Communication Based Technology (ICT)

Start date: November 2015
Phase: N/A
Study type: Interventional

This project develops a new form of management of subjects with suspected SAHS and different sleep disorders by applying Information and communications technologies (ICT).

NCT ID: NCT02762916 Completed - Clinical trials for Peripheral Arterial Disease

CONTECI Program: A New Way to Control Peripheral Arterial Disease Using New Technologies

Start date: May 2014
Phase: N/A
Study type: Interventional

The current increase in chronic diseases calls for changes to the health system. It is necessary to promote expert patient in chronic disease. The expansion of new technologies gives us new tools to face new challenges, providing efficiency, expertise and autonomy. The characteristics of peripheral arterial disease make possible to promote expert patient and the self-management. In order to bring these concepts together the telemedicine program was created to promote expert patient for increasing the quality of life and satisfaction of patients and improving the efficiency of the health system. Methods: Randomized clinical trial on patients with peripheral arterial disease in intermittent claudication grade. They were randomized into two groups: intervention arm (IA) using CONTECI program for self-managing and control arm (CA), followed as usual vascular visits.

NCT ID: NCT02644343 Completed - Telemedicine Clinical Trials

Safety and Efficacy of Remote Programming of Nucleus Cochlear Implants

TEL
Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the safety and efficacy of Nucleus cochlear implant programming via telecommunication.

NCT ID: NCT02591602 Completed - Telemedicine Clinical Trials

Teleradiology Program for Frail Patients Living at Home or in Nursing-homes

RADHOME
Start date: November 2011
Phase: N/A
Study type: Interventional

Transporting radiology to the patient's home is challenging. Preliminary experiences conducted in Turin (Italy) and Lund (Sweden) indicate that the coupling of simple, light-weight X-ray equipments with a Computed radiography or Digital Radiography systems could be effective for externalization of radiographic service. The image and examination quality has been proved to be the same than those performed with a stationary equipment and analysis on safety of radio-protection systems show a very low risk exposure for health staff as well as for the general population. Mobile radiography in nursing homes has shown to be technically feasible and the most beneficial results were that patients avoided unnecessary transport back and forth to the hospital; in both experiences the majority of patients could be treated locally. The key points of RADHOME project are two: 1. The first one is to built a network model, with the aim to disseminate clinical use of domiciliary radiology. 2. The second one is to demonstrate clinical efficiency and cost-effectiveness of domiciliary radiology.

NCT ID: NCT02344082 Completed - Telemedicine Clinical Trials

Pharmacists Provide Telemedicine in Addition to Clinic Visits to Improve Diabetes Management

Start date: January 2015
Phase: N/A
Study type: Interventional

This prospective study will include both an intervention and control arm. The control arm will receive face-to-face pharmacy clinic visits per standard of care. The intervention arm will receive pharmacy clinic visits plus additional telephone follow-up. Patients with a hemoglobin A1c in the last 3 months greater than 9% will be eligible. Eligible patients must have a primary care physician at Johns Hopkins Outpatient Center (JHOC) or East Baltimore Medical Center (EBMC). Purpose: To compare the change in hemoglobin A1c over the 3 month study period in the intervention group in which patients participate in telemedicine, to a control group in which they do not

NCT ID: NCT02196428 Completed - Telemedicine Clinical Trials

Medical Telemonitoring Plus Individual Teleconsultation in Elderly

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of this study is to explore the requirements and conditions of medical teleconsultation and remote diagnostics (telemonitoring) of older people in the residential environment with an emphasis on the need for adaptation, feasibility and acceptance of telemedicine services to a web based documentation and communication platform (Ambient Assisted Living Wizard).