Royce Sampson

ORCID: 0000-0001-7788-6215
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About
Contact & Profiles
Research Areas
  • Health and Medical Research Impacts
  • Ethics in Clinical Research
  • Health Systems, Economic Evaluations, Quality of Life
  • Dementia and Cognitive Impairment Research
  • Healthcare Decision-Making and Restraints
  • Open Source Software Innovations
  • Schizophrenia research and treatment
  • Opioid Use Disorder Treatment
  • Scientific Computing and Data Management
  • Research Data Management Practices
  • Biomedical and Engineering Education
  • Health Policy Implementation Science
  • Advances in Oncology and Radiotherapy
  • Psychiatric care and mental health services
  • Posttraumatic Stress Disorder Research
  • Migration, Health and Trauma
  • Innovation Policy and R&D
  • Substance Abuse Treatment and Outcomes
  • Alzheimer's disease research and treatments
  • Child Abuse and Trauma
  • Academic Publishing and Open Access
  • Biomedical Ethics and Regulation
  • Research, Science, and Academia
  • Meta-analysis and systematic reviews
  • Mobile Crowdsensing and Crowdsourcing

Medical University of South Carolina
2008-2024

Clinical Research Professionals (CRPs) are essential members of the and Translational Workforce. Many academic medical institutions struggle to recruit retain these vital team members. One strategy increase job satisfaction promote retention CRPs is through educational initiatives that provide training professional development. The South Carolina (SCTR) Institute Workforce Development (WD) at Medical University (MUSC) developed several trainings as part our larger portfolio for CRPs. In 2022...

10.3389/fphar.2023.1304415 article EN cc-by Frontiers in Pharmacology 2024-01-08

ClinicalTrials.gov is a web-based resource which provides the general public, healthcare professionals, patients, and caregivers access to privately publicly supported clinical trials trial results. The web site maintained by National Library of Medicine (NLM) at Institutes Health (NIH) (ClinicalTrials.gov Background, 2018). penalties for non-compliance with legal obligations under FDAAA 801 (Food Drug Administration Amendments Act 2007) NIH requirements registering reporting results on...

10.1016/j.conctc.2020.100557 article EN cc-by-nc-nd Contemporary Clinical Trials Communications 2020-03-17

A behavioral intensive care unit was originally designed as a 21-day inpatient program for treating agitation among demented patients, one of the most common disorders in this group. Due to need dramatically reduce length stay and create alternative environments, original model modified into an integrated continuum blending outpatient partial hospitalization that reduced from 21 average seven days. This quasiexperimental study compared effectiveness continuum-of-care programs conducted cost...

10.1176/ps.48.11.1435 article EN Psychiatric Services 1997-11-01

Quality assurance (QA) of clinical trials is essential to protect the welfare trial participants and integrity data collected. However, there little detailed information available on specific procedures outcomes QA monitoring for trials.This article describes experience National Institute Drug Abuse's (NIDA) Abuse Treatment Clinical Trials Network (CTN) in devising implementing a three-tiered model rigorous multi-site randomized implemented community-based substance abuse treatment programs....

10.1177/1740774509102560 article EN Clinical Trials 2009-04-01

We evaluated the impact of a regulatory support service (known as Regulatory Knowledge and Support [RKS] program), part Medical University South Carolina’s Clinical Translational Science Award, on success Institutional Review Board (IRB) applications that have previously been deemed by IRB to be Not Ready for (NRR). At time this evaluation, 77 studies had NRR, 53 which came from trainees junior faculty. All received either approval or were not research, therefore did require review. In all,...

10.1177/1556264617752725 article EN Journal of Empirical Research on Human Research Ethics 2018-01-18

Low-accruing clinical trials delay translation of research breakthroughs into the clinic, expose participants to risk without providing meaningful insight, increase cost therapies, and waste limited resources. By tracking patient accrual, Clinical Translational Science Awards hubs can identify at-risk studies provide them support needed reach recruitment goals maintain financial solvency. However, accrual has proved challenging because relevant patient- protocol-level data often reside in...

10.1017/cts.2022.382 article EN cc-by-nc-nd Journal of Clinical and Translational Science 2022-01-01

Hybrid academic-business models are evolving in CTSA clinical research units.

10.1126/scitranslmed.3003589 article EN Science Translational Medicine 2012-07-04

Integrated, real-time data are crucial to evaluate translational efforts accelerate innovation into care. Too often, however, needed fragmented in disparate systems. The South Carolina Clinical & Translational Research Institute at the Medical University of (MUSC) developed and implemented a universal study identifier-the Master Identifier (RMID)-for tracking research studies across systems warehouse-inspired model-the Integrated Network Systems (RINS)-for integrating from those systems.In...

10.1093/jamia/ocab023 article EN Journal of the American Medical Informatics Association 2021-01-28

SPARCRequest© (Services, Pricing, & Application for Research Centers) is a web-based research management system that provides modular and adaptable "electronic storefront" research-related services. Developed by the South Carolina Clinical Translational Institute at Medical University of Carolina, it was released as open source (OS) code in 2014. The adoption accelerated 2016, when, to ensure responsiveness needs partners, its governance also became open. This model enables OS partners...

10.1017/cts.2019.403 article EN cc-by-nc-nd Journal of Clinical and Translational Science 2019-08-27
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