Detailed Information on Publication Record
2024
Training and education on inclusivity in clinical trials-the SENSITISE project
SHIELY, Frances, Jitka RYCHLÍČKOVÁ, Christine KUBIAK, Zora ČECHOVÁ, Martina ESDAILE et. al.Basic information
Original name
Training and education on inclusivity in clinical trials-the SENSITISE project
Authors
SHIELY, Frances, Jitka RYCHLÍČKOVÁ (203 Czech Republic, belonging to the institution), Christine KUBIAK, Zora ČECHOVÁ (203 Czech Republic, belonging to the institution), Martina ESDAILE and Shaun TREWEEK
Edition
Trials, LONDON, Elsevier, 2024, 1745-6215
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30230 Other clinical medicine subjects
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.500 in 2022
Organization unit
Faculty of Medicine
UT WoS
001222713100001
Keywords in English
clinical trials; training; education
Tags
International impact, Reviewed
Změněno: 11/7/2024 13:40, Mgr. Tereza Miškechová
Abstract
V originále
There have been calls globally to improve participation in clinical trials of groups that traditionally have been under-represented. These under-served groups are populations under-represented or disengaged from medical research or services despite having a disproportionately high healthcare burden. INCLUDE, a 2017 initiative from the UK’s National Institute of Health Research (NIHR), has defined and identified under-served groups in clinical trials (elderly, ethnic minorities, the socioeconomically disadvantaged, pregnant and lactating women, the LGBTQ+ community, rural dwellers, those with comorbidities including disability, mental health conditions or cognitive impairment, amongst others) and barriers for recruitment. Trial conclusions cannot with certainty support treatment decisions (or mode of treatment delivery) for those not represented in the trial. This perpetuates inequality, is immoral and represents bad science. It can also lead to general distrust in research amongst under-served groups. Designing and conducting clinical trials is a complex task, and all involved agree that investigators need adequate training to perform their duties. Despite this, there is no formal training on inclusivity in clinical trials available globally.