Dr. Chitra Lalloo
@lallooc
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SickKids Research Lead for @ECHOPaeds and iCanCope with Pain. Co-Chair of Research @SKPainCentre. Faculty, @ihpmeuoft. Proud Hamiltonian/South African.
Toronto, Ontario
Joined May 2012
Proud to share 1st 🇨🇦 pediatric study using @Apple #researchkit to deliver remote #econsent for #mhealth research! @CAFsociety @SickKidsNews @DrJenStinson @qthipie @JosephCafazzo
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Are you working on innovative projects at the intersection of pediatric cancer and pain? 🌟 @SickKidsCancer and @SKPainCentre are funding 2 seed grants, each with a maximum budget of $10K CAD! 🗓️ Due date: February 28, 2025, at 5:00 PM ET 📩For more info: https://t.co/YOi1QAjkwq
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It's National Pain Awareness Week! With 1 in 5 Canadians living with #ChronicPain, access to quality care should be available to everyone, regardless of race, sex, gender, culture, or any other identity🏥 #NPAW2024
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📢 We are seeking proposals for a Seed Grant Competition focused on sex and gender disparities in pediatric pain. 🩺💡 🗓️ Deadline: December 2, 2024 💰 Funding: Up to $10,000 CDN for innovative clinical research projects. For more info: https://t.co/qbY9Mw2xRt
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As part of a national initiative, we’re excited to launch a new #ECHO pilot series that will focus on #opioids and #substance use in the context of managing #pain. Learn more & register: https://t.co/1AZFMIfZBA
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Check out our publication! We adapted a #ChronicPain questionnaire for the #TransitionalPain setting through #pediatric patient & family feedback. Grateful for this team! @DrLisaIsaac @JenniferTyrre14 @lallooc @rachelgoren @SKAnesthesia
#PatientEngagement
https://t.co/LjgIdScIej
jpro.springeropen.com
Background Patient engagement is an important tool for quality improvement (QI) and optimizing the uptake of research findings. The Plan-Do-Study-Act (PDSA) model is a QI tool that encourages ongoing...
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For the past 5 years, the leads and community of practice of @ECHOPaeds #Pain have been committed to sharing the most up-to-date evidence-based knowledge for managing pain in children & youth. This is how we #PrioritizePain and fit in the #PainPuzzle. #NPAW2022 #MindingPain2022
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Vote for our video in the @CIHR_IHDCYH 2022 Video Talks Competition! Proud to share our work on the Power over Pain Portal for Youth, co-designed w/ youth across Canada living with pain. Vote by liking it on YouTube: https://t.co/66AdODcqcJ
@iOuchLab
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Come join us @CriticalQual on Friday for my seminar on critical qualitative case study methodology and find out why you should use case study for your next project!!
We're back! On October 7, @tieghank will present "Critical Qualitative Multiple-Case Study: A Methodological Mouthful", as part of CQ's Virtual Seminar Series. Learn more and register: https://t.co/FNBEiYSEn7
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Really proud to launch this survey. @clinicaltrialON's College of #LivedExperience was critical to developing this survey where we hope to learn Canadians' preferences about 'decentralized' #ClinicalTrials. It's open to anyone in Canada over 18 years (Alt text in next tweets)
CTO wants to hear from you! We invite you to participate in a #Survey so that we can understand your opinions related to being in a decentralized #ClinicalTrial. Learn more about the study here: https://t.co/2Ih5Q3uM6G
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On now and just in time for #SickleCellAwarenessMonth ! Pop by poster 215 @IASPpain to meet the fabulous @VinaMohabir and learn about our study of engagement with digital pain self-mgt among youth and caregivers with sickle cell disease.
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The latest The #digitalhealth Daily! https://t.co/FsGFq6gsKk Thanks to @lallooc @leni_las #protocol #ltc
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📲🏥What’s next? Our team is refining the program based on participant feedback. We will then be studying the implementation of iCanCope in partnership with sickle cell clinics and community organizations.(6/6)
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🔍What did we find?🔎 Interviews revealed that most dyads would continue to use the program (92%) and recommend it to others (83%). Caregivers would recommend the program to others living with SCD who were newly diagnosed or who frequently experienced pain crises. (5/6)
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🔍What did we find?🔎 Youth with sickle cell disease reported that the program helped to facilitate self-management behaviors such as goal setting, applying strategies for pain management, symptom trend monitoring, and learning through peer support. (4/6)
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🔍What did we find?🔎 Youth were more likely to engage with the iCanCope app (85%) than the website (68%). Reasons for app preference included greater ease of use, acceptable time commitment, and more interactivity. (3/6)
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User-centred design was used to tailor the iCanCope digital pain self-management program for sickle cell disease. Our randomized controlled trial enrolled a cohort of majority Black (93%) youth and caregivers from a range of economic backgrounds. (2/6)
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https://t.co/EIfS0LhQEX Our new paper, featured at @IASPpain (poster 215 on Friday), describes one of the first studies to apply digital health analytics to characterize patterns of engagement with pain self-management among youth and caregivers with sickle cell disease. (1/6)
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Are you a MD or NP with expertise in pediatric pain? 👀 We are inviting you to tell us what you think about a new screening tool for neuropathic pain and complex regional pain syndrome called the Pediatric PainSCAN. Click here for more info > https://t.co/RayBUYWfEZ
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RT if you can hear these images. Happy Birthday, Catherine O'Hara 🎉
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