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Clinical research generally involves in-person participant visits. Study participants are provided study information leading to their signature on a consent form. They are often required to have lab...

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Clinical research generally involves in-person participant visits. Study participants are provided study information leading to their signature on a consent form. They are often required to have lab samples taken for safety and efficacy purposes in drug development trials.

Question: How would you manage a clinical trial during COVID when in-person visits may not be an option?

Think about telemedicine and remote monitoring

Answered 1 days After Nov 02, 2021

Solution

Sanjukta answered on Nov 04 2021
121 Votes
Running Head: HEALTHCARE
HEALTHCARE 7
HEALTHCARE
Introduction
It is a known fact that the clinical research mainly involves the in-person visits. The participants of the study are provided with the information that leads toward providing signature in a consent form. Furthermore, they are also required for having lap samples taken for the efficacy and safety purposes in the trials for the drug development.
Body
It has been observed that more 1 year ago the clinical trials were all of a sudden as well as significantly disrupted by the pandemic. The restrictions due to the pandemic that prevented or restricted the in-person visits resulted in the unprecedented ba
iers toward the data collection, enrolment of trial, along with the intervention delivery for a lot of clinical trials. On the other hand, there are a lot of investigators of the clinical trial that replaced the in-person interactions with the alternative approaches conducted remotely. Throwing light on the above-mentioned discussion it can be stated that clinical trial during COVID-19 pandemic can be managed with the help of the remote monitoring and telemedicine (McDermott & Newman, 2020).
In general remote monitoring tends to involve the evaluation of the off-site that is performed by the monitor away from the site at which the clinical trial is being conducted. During this time remote access holds a lot of importance in terms of continuing the clinical trials without any disruption that were preserving and in progress subject safety throughout this important and crucial time. It is expected by the healthcare professionals it is expected that remote monitoring to become one of the most important element concerning the clinical trial conduct fastest moving. In case of the remote monitoring some of the devices are used for transmitting and capturing the biometric data. For instance, a tele-electroencephalogram device is able to monitor the electrical activity of the
ain concerning an individual as well as then transmitting those data to a specialist that is assigned to the case. This cooperation could happen either continuously or as a put-away and afterward sent the transmission. Instances of telemonitoring incorporate the following: Monitoring patient boundaries during locally situated night-time dialysis Cardiac and multiparameter checking of far off serious consideration units (ICUs)Home telehealth—for instance, every day home telemonitoring of fundamental signs by patients and ensuing transmission of those information that empowers offsite attendants to follow their patients routinely and unequivocally and address perceptible changes through instruction and data ideas about diet or exercise (McDermott & Newman, 2021). After observing the effectiveness the remote monitoring will be highlighting a lot of enhancements in terms of studying effectiveness, efficiency, as well as possibly overall costs when contrasted for presenting monitoring plans that also requires a prolonged visit on-site by a study monitoring from the coordinating centre. Furthermore, remote monitoring activities, consisting of the remote review in terms of the source documents, must be documented in the...
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