Sarah Gil

ORCID: 0000-0002-2517-2912
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About
Contact & Profiles
Research Areas
  • Mobile Health and mHealth Applications
  • Diabetes Management and Education
  • Health Literacy and Information Accessibility
  • Clinical practice guidelines implementation
  • Chronic Disease Management Strategies
  • Acute Kidney Injury Research
  • Primary Care and Health Outcomes
  • Dialysis and Renal Disease Management
  • Healthcare cost, quality, practices
  • Healthcare Decision-Making and Restraints
  • Hip and Femur Fractures
  • Pharmaceutical Practices and Patient Outcomes
  • Medication Adherence and Compliance
  • Renal and Vascular Pathologies
  • Childhood Cancer Survivors' Quality of Life
  • Ethics in Clinical Research
  • Health Policy Implementation Science
  • Schizophrenia research and treatment
  • Telemedicine and Telehealth Implementation
  • Health Systems, Economic Evaluations, Quality of Life
  • Diabetes Management and Research

University of Calgary
2016-2024

Angela Ju Mark L. Unruh Sara N. Davison Juan Dapueto Mary Amanda Dew and 94 more Richard Fluck Michael J. Germain Sarbjit V. Jassal Gregorio T. Obrador Donal O’Donoghue Michelle A. Josephson Jonathan C. Craig Andrea K. Viecelli Emma O’Lone Camilla S. Hanson Braden Manns Bénédicte Sautenet Martin Howell Bharathi Reddy Caroline Wilkie Claudia Rutherford Allison Tong Adeera Levin Andrew S. Narva Angela Yee‐Moon Wang Angelique F. Ralph Annette Montalbano Moffat Barry Bell Brenda R. Hemmelgarn Brigitte Schiller Carmel M. Hawley Christen Perry Christoph Wanner Daniel Cukor Daniel Pérez Plasencia David Cella David A. Harris David W. Johnson David A. Roer David Van Wyck David C. Wheeler Deborah Deyhle Derrick Gill Dori Schatell Elena Bavlovlenkov Eric D. Weinhandl Fergus Caskey Francesca Tentori Giorgos K. Sakkas Harvey Saver H. Gideon Wells James Wadee Jamilah Akbar Jane Carter Jennifer E. Flythe Jenny I. Shen John W. Kusek John Gill Joyce Beverly J Pintér Kirsten L. Johansen Klemens B. Meyer Leonard Lirtzman Linda Wagner‐Weiner Luigi Costabile Manisha Jhamb Marcello Tonelli Marinella Ruospo Martin Howell Maurizio Bossola Michael J. Thomas N H Segura Méndez Neil R. Powe Nieltje Gedney Noah Rouse Pamela Kaden Peter G. Kerr Peter Tugwell Quinetta Taylor Rachel Sand Roberto Pecoits–Filho Sally Crowe Sarah Gil Sheila G. Jowsey‐Gregoire Stephen Z. Fadem Stephen P. McDonald Steven D. Weisbord Suetonia C. Palmer S. Susan Hedayati Tess Harris Thomas F. Hiemstra Uthma Muhammed Vanessa McNorton Vanja Sikirica Vivekanand Jha William G. Herrington Wim Van Biesen Wolfgang C. Winkelmayer­ Zeeshan Butt

10.1053/j.ajkd.2017.12.018 article EN American Journal of Kidney Diseases 2018-03-18

Background Supporting patients to self-manage their chronic kidney disease (CKD) has been identified as a research priority by with CKD and those who care for them. Self-management shown slow progression improve the quality of life individuals living disease. Previous work need person-centered, theory-informed, web-based tool self-management that can be individualized patient’s unique situation, priorities, preferences. We addressed this gap using an integrated knowledge translation method...

10.2196/22220 article EN cc-by JMIR Formative Research 2020-12-12

<sec> <title>BACKGROUND</title> Care for mild to moderate chronic kidney disease (CKD) entails self-management from patients and clinical support primary care nephrology. In response a gap in resources this population, My Kidneys Health was co-developed of CKD. While is patient-facing tool, health providers play critical role the implementation patient </sec> <title>OBJECTIVE</title> This study develops evaluates strategies implement into routine general nephrology care....

10.2196/preprints.71832 preprint EN cc-by 2025-01-27

There is limited research of electronic tools for self-management patients with chronic kidney disease (CKD). We sought to evaluate participant engagement, perceived self-efficacy and website usage in a preliminary evaluation My Kidneys Health, patient-facing eHealth tool Canada.We conducted an explanatory sequential mixed-methods study adults CKD who were not on replacement therapy had access Health 8 weeks. Outcomes included acceptance (measured by the Technology Acceptance Model), Chronic...

10.9778/cmajo.20210332 article EN CMAJ Open 2022-07-01

AbstractBackground:Chronic kidney disease (CKD) clinics across Canada provide tailored care for patients with CKD an aim to slow progression and prevent complications. These self-management resources; however, there is limited information about what resources are being used by clinics. We undertook a survey of identify adults aged 18 years over categories 1 5 not requiring dialysis or transplant.Objective:To collate (eg, strategies, tools, educational materials) (categories 5, replacement...

10.1177/2054358118775098 article FR cc-by-nc Canadian Journal of Kidney Health and Disease 2018-01-01

Nephrology was previously identified as a subspecialty with few Canadian employment opportunities, and in recent years, fewer trainees are choosing nephrology.The objective of this study is to better understand the current adult nephrology workforce expected trends over next 5 years.This an online self-administered survey.This set Canada.Survey participants nephrologists, including self-identified division heads.The measurements demographics, training, practice characteristics, work hours,...

10.1186/s40697-016-0117-6 article FR cc-by-nc Canadian Journal of Kidney Health and Disease 2016-01-01

Abstract Introduction People with chronic medical conditions often take medications that improve long‐term outcomes but which can be harmful during acute illness. Guidelines recommend healthcare providers offer instructions to temporarily stop these when patients are sick (i.e., days). We describe the experiences of managing days and providing day guidance their patients. Methods undertook a qualitative descriptive study. purposively sampled from across Canada. Adult were eligible if they...

10.1111/hex.13789 article EN cc-by Health Expectations 2023-06-08

ABSTRACT Introduction High-quality clinical trials are needed to establish the safety, efficacy, and real-world use of potential therapies for acute kidney injury (AKI) prevention. In this consensus workshop, we identified patient caregiver priorities recruitment, intervention delivery, outcomes a trial cilastatin prevent nephrotoxic AKI. Methods We included adults with lived experience AKI, chronic disease, or risk factors AKI (e.g., critical care hospitalization), their caregivers. Using...

10.1101/2024.03.04.24303721 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-03-05

Key Points For AKI prevention trial recruitment, patients prioritized technology enabled prescreening and involvement of family members in the consent process. intervention delivery, participants measures to facilitate ease administration return visits. outcomes, patient identified effects on kidney-related other clinical outcomes as top priorities. Background High-quality trials are needed establish efficacy safety novel therapies for prevention. In this consensus workshop, we caregiver...

10.34067/kid.0000000000000554 article EN cc-by-nc-nd Kidney360 2024-08-15

<sec> <title>BACKGROUND</title> Supporting patients to self-manage their chronic kidney disease (CKD) has been identified as a research priority by with CKD and those who care for them. Self-management shown slow progression improve the quality of life individuals living disease. Previous work need person-centered, theory-informed, web-based tool self-management that can be individualized patient’s unique situation, priorities, preferences. We addressed this gap using an integrated knowledge...

10.2196/preprints.22220 preprint EN 2020-07-06
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