|drug3331||Tele-delivered psychological intervention Wiki||1.00|
|D013313||Stress Disorders, Post-Traumatic NIH||0.19|
There is one clinical trial.
Covid-19, a commonly severe respiratory tract infection caused by the SARS-CoV2 Coronavirus, poses an increasing threat to individual health and health care systems. The individual disease course ranges from mild to life threatening, the pandemic spread leads to a shortage of health care resources including intensive care availability. It should be the overarching goal to allocate sparse health care resources to those most at need and to simultaneously avoid unnecessary blocking of resources by clinically unjustified hospitalizations. Individuals with preexisting cardiovascular conditions are at the highest risk of health deterioration, even at younger age. Objective criteria for hospitalization are not immediately available in a outpatient settings. Hence, hospitalization and emergency medical contact is often triggered by subjectively interpreted symptoms. The goal of this project is thus to improve the availability of objective measurements in the outpatient setting by means of an innovative, smartwatch mediated telemedicine approach. To achieve this goal, the investigators will conduct a randomized clinical trial comparing a smartwatch based telemedicine intervention with standard of care. The intervention group will receive regular objective measurements of heart rate, ECG, and SpO2 and will get access to a 24/7 medical care hotline for consultation. The investigators hypothesize that the intervention group will benefit by a significant reduction in unnecessary hospitalizations and unplanned emergency medicine contacts.
Description: Occurrence of any of the above during follow-upMeasure: Rate of participants with a combination of hospitalization and unplanned use of hospital emergency department or emergency medical service Time: 30 days
Description: Occurrence of hospitalization during follow-upMeasure: Rate of participants hospitalized Time: 30 days
Description: Occurrence of any of the above during follow-upMeasure: Rate of participants with unplanned use of hospital emergency department or emergency medical service Time: 30 days
Description: Occurrence of death of any cause during follow-upMeasure: Rate of participants experiencing death of any cause Time: 30 days
Description: Occurence of daeth of Covid-19 during follow-upMeasure: Rate of participants experiencing death of Covid-19 Time: 30 days
Data processed on January 01, 2021.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.Drug Reports MeSH Reports HPO Reports