Name: Patient Perspectives to Improve Retention with eConsent
Start: 2022-02-22T16:00:00Z
End: 2022-02-22T16:00:52.000Z
Location: BrightTALK
Rating: 5

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Join us on 20th May, which marks Clinical Trials Day, as we ask – how can we better understand the patient experience for better clinical trial outcomes?

In our upcoming webinar, we are delighted to be joined by Mark Doyle, Founder, A Life in a Day and Emma Sutcliffe, VP, Head Global Patient Affairs, Ipsen, discuss the transformative journey of clinical trials and the pivotal role patient-centric approaches play in enhancing outcomes.

Join us as Emma shares her insights, shedding light on how a patient-centric focus has become integral to the development and deployment of clinical trials at Ipsen. Delve into practical strategies employed by Emma and her team at Ipsen, supported by immersive learning strategies explored by Mark, to place patients at the forefront of their trials, ultimately elevating the quality and effectiveness of the research.

We will also be diving into the outcomes of employing these strategies, with both speakers sharing insights into the outcomes achievable by better understanding the patient experience and using empathy to drive better outcomes in trials.

Participate in this on-demand webinar to:

• Foster collaboration with patients for enhanced trial outcomes.
• Gain firsthand insights into effectively understanding and addressing patient challenges within trials.
• Explore innovative approaches to design and execute trials with a heightened focus on patient needs.

Clinical Trials: How effective patient engagement shapes key decision making

Recent trends in corporate governance (CG) and M&A are presenting great opportunities for expansion of gaming businesses globally. Increasingly, we are witnessing legalization of gambling and greater regulation in other emerging jurisdictions. All this, at the same time, represents major challenges for transnational gaming companies: How to maintain the highest compliance standards and best industry practices in those jurisdictions that have lax or developing regulations? How can preventive, effective and achievable CG controls be established so as not to incur sanctions that jeopardize the licenses of international major operators in their countries of origin with stricter regulations?

Moderated by Michael Bonner, a Shareholder with Greenberg Traurig, the panelists are:
• Sam Basile, Vice President - North America Gaming & Licensing, GeoComply
• Alfredo Lazcano, Partner, Lazcano Samano
• Stephen Martino, Senior Vice President & Chief Compliance Officer, MGM Resorts International
• Steve Kastner, Vice President of Compliance, PlayDigital, IGT

Ensuring compliance in less regulated jurisdictions

Launching a treatment is a complex process that involves maximizing impact for all stakeholders, from providers to patients. It requires the strategic alignment of each pivotal moment, from regulatory approvals to medical and patient engagement, to launch strategy. Our panel of experts will share valuable insights on the key challenges often faced and solutions on how to ensure your product launch journey is tracked for success.

Ryan Quigley, Chief Operating Officer, Inizio 
Terri Harchar, Managing Director, Nazare (NA), Inizio Engage 
Sese Abhulimen, President Global Decision Optimization, Propensity4 an Inizio Engage Company  
Shauna Aherne, President, Medical Excellence, Medistrava, Inizio Medical 
Brian Stamm, Executive & Product Launch Service Lead, Vynamic, An Inizio Advisory Company 
Will Reese, Chief Innovation Officer, Inizio Evoke 
Scott Briggs, Principal, Putnam an Inizio Advisory Company

Key product launch challenges: creating a successful product launch

In the landscape of the clinical trial industry in 2024, persistent challenges persist in the realms of patient recruitment and retention. These hurdles, having endured over several years, continue to pose significant obstacles. As we navigate through the complexities of the current year, experts in the field—namely, Kate Shaw, Leanne Whoehlke, and Will Krugman—will delve into pivotal aspects of patient recruitment and retention challenges. The discussion will intricately explore strategies to augment awareness of clinical trials within the broader public sphere, contemplating innovative approaches to engage with local communities. The focus remains steadfast on ensuring that patient recruitment and retention remain robust throughout the clinical trials course. This discourse promises to illuminate and address critical issues, propelling the clinical trial industry toward enhanced efficacy and patient-centred success.

Kate Shaw - Founder & CEO, Innovative Trials
Leanne Woehlke - Director, Life Sciences Solutions, TransPerfect
Will Krugman - Marketing & Communications Director, Clinical Research Associates

Patient Recruitment & Retention Strategies in the 2024 Clinical Trial Landscape

WorldSkills UK is a world-class skills network focused on raising standards, championing future skills and empowering young people from all backgrounds.  

We have big ambitions to help the next generation, our education system and the economy. From raising self-esteem through to providing opportunities to develop skill levels further and benchmark training delivery. WorldSkills UK tools and resources play a vital role in teaching and learning environments by complementing different approaches to Teaching, Learning and Assessment and bringing learning to life. 

Embedding excellence in technical and vocational education: Teaching and assessment webinar offers an introduction to embed the WorldSkills UK teaching tools and careers education at the right time into the curriculum to help young people grow personally and professionally, developing their technical and employability skills. Including guidance on how to access world-class teacher training through the WorldSkills UK Centre of Excellence and the diverse range of support offered through the Network for Innovation, equipping leaders and teaching practitioners with the knowledge and skills to raise the quality and standards within their provision. 

As a result of embedding world-class practice amongst your learners, they will be equipped to participate in the WorldSkills UK national competitions, using insights from our international competitions to help learners and apprentices be armed with world-class skills employers' demand.

Embedding excellence in technical and vocational education:Teaching & assessment

Play improves the social, emotional and cognitive wellbeing of children and young people. Research suggests that children actually learn best through play, helping them to develop confidence, learn new skills and reduce feelings of stress or anxiety. 

So how can you use play to help neurodivergent children to thrive?

Join Dr Gina Gómez de la Cuesta, Clinical Psychologist and Founder of Play Included®, at 2.00pm (UK time) on Thursday 15 February to learn how you can use collaborative LEGO® play to support the children you work with. 

In this webinar, you will learn: 
• Research into learning through play
• How to support neurodivergent children in their play
• How to identify if LEGO brick based therapy is suitable for the children you work with 

Gina is co-founder of Play Included®, which provides training programmes for education and health professionals to implement the Brick-by-Brick® programme, a neurodiversity-affirming social skills therapy using LEGO bricks that was developed in partnership with, and is officially endorsed by, the LEGO Foundation.

Supporting neurodivergent children through play

15 about brick

*To ensure this webinar caters to your specific interests, we would greatly appreciate it if you could spare just 2 minutes to complete a brief survey after registering. Your input matters to us: https://www.surveymonkey.co.uk/r/DFWLXGM

Clinical trial patient recruitment and retention remains one of the key challenges to successfully bringing a new therapeutic to market. An estimated 85% of clinical trials face delays due to enrolment issues [1,2], and poor recruitment is a common reason for discontinuation [3]. Of those successfully enrolled, around 30% are likely to drop out [4], which increases costs for sponsors and threatens the viability of the trial itself.

Directly supporting patients from prescreening to study endpoint can help minimize delays and safeguard against early termination, but this can be difficult for hard-pressed sites. Join us as we discuss the most common patient support challenges – as described to us by YOU – and how our new Navigator service can solve them by giving patients a more personalized clinical trial experience and consistent contact, alleviating the burden on sites, and ensuring a sponsor’s study runs efficiently to help accelerate patient access to life-changing treatments.

We will share our insight into why the ‘human touch’ can elevate your in-study patient engagement to the next level and how this permeates through our Navigator service to benefit patients, sites and sponsors. You will also hear from a sponsor that has benefitted from our expertise: the difficulties they faced, the solutions we implemented and the difference we made. And we will share feedback from clinical trial participants about what they think of our support.

Speakers
Chair John Pinching, Editor, PharmaTimes
Laura Burt Director of Operations, Innovative Trials
Kari Reilly Site Operations Lead, Innovative Trials
Helen Andrews Global Clinical Trial Manager, Avillion
Amy Lopez Navigator, Innovative Trials

Solving your biggest patient recruitment and retention challenges

The presence of so-called “grey-market machines as illegal ways to gamble continue to create legal and regulatory issues for the gaming industry, as operators and regulators grapple with how to address a wide range of alternative ways to gamble including illegal slot machines operating as “games of skill.”  In addition, there has been a considerable expansion of “free to play” od co-called “social casino” gaming options in the US markets.  This panel will provide an update on the existing US legal challenges against the gray market and evaluate what regulators and operators can do together to combat the proliferation of “gray” slot machines.  In addition the panel will update how peer-to-peer skill game contests, freemium gaming (a/k/a “social casinos”), and daily fantasy sports variants remain unregulated but have been challenged by civil litigation, and similar issues being faced around the world.

Moderated by Bill Gantz, a Partner with Duane Morris, the panelists include:
• Daron Dorsey, Executive Director, AGEM
• Wulf Hambach, Partner, Hambach & Hambach
• Jeff Morris, Vice President – Public Affairs & Government Relations: PENN Entertainment
• Michael Pollock, Senior Policy Advisor, Spectrum Gaming Group

The Blurred Lines between Legal, Grey and Illegal Ways to Play

Technology is a driving component of the growing online sports betting and iGaming landscape in the U.S. and globally. The rise in uses of technology for operational purposes has also created opportunities to enhance compliance processes. From financial crime detection and anti-fraud measures to exploring data outputs for responsible gaming purposes, technology solutions focus on how an increasingly accessible amount of data can be leveraged for compliance efficiencies and regulatory expectations. How are systems being utilized to capture relevant information? How does the increasing focus on artificial intelligence play into solutions? Hear from industry leaders as they discuss their experiences, uses of technologies and their thoughts on applicability for compliance purposes.  

Moderated by Bob Boyle, Senior Manager at EY, the panelists are:
·         Gabrielle Angle, Director – Government Relations & Licensing at GeoComply
·         Patrick Bland, Chief Technology Officer at Acres Technology
·         Laura McAllister Cox, Chief Compliance Officer, Rush Street Interactive
·         Will Monk, Chief Product Officer, Napier

How Technology is Playing a Significant Role in Gaming Compliance Programs

Putting the patient first has never been higher up the agenda throughout the drug development process, but can we further fine-tune our approach?

Tune into this webinar where we ask:
• How important is early patient engagement to business success.
• How do you ensure the patient voice is as ‘loud’ in later stages
• Whose responsibility is it to ensure the patient voice is heard

Viewers will come out with a deeper understanding of how to best keep the patient voice alive through all stages of drug development.

Keeping the patient voice alive through all stages of drug development

For clinical trial participants, navigating their way through a study can sometimes seem daunting and complicated. Without the right support, around 30% are likely to drop out [1], resulting in extra financial costs for sponsors and potentially placing the future of the trial in jeopardy.

However, sites don’t always have the time and resources available to commit to ongoing and consistent patient engagement. In our upcoming webinar, we will discuss common challenges participants and sites face when it comes to engagement and how our new ‘Navigator’ service is helping to change the game.

Hear how our new patient-centric service benefits patients, sites and sponsors by
ensuring patients get the support they need for the best clinical trial experience possible
decreasing the risk of early trial termination by improving the retention of participants until the very end of a study
reducing the burden on sites by performing a second layer of pre-screening, allowing sites to focus on the science.

Speakers:

Chair - John Pinching, Editor at PharmaTimes
Kari Reilly - Patient Recruitment Manager, Innovative Trials
Kristin Faber - VP of Clinical Trial Patient Recruitment, Spectrum Science
Adel Sepulveda - Patient Navigator, Innovative Trials
TBC - Site

Navigating patients step by step on their clinical trial journey

Marketing surrounding online sports betting is a constantly evolving landscape.  From licensing to the review of advertising language and prohibited phrases, the U.S. has seen many different approaches to this area.  Can the industry successfully regulate itself or will regulators need to step in to police the market?  Are the recent fines levied in Ohio a sign of a changing regulatory perspective?  Will there be a ripple effect in other regulated jurisdictions where previously regulation on marketing was light-touch?  Hear from experts in the industry discuss their thoughts on the future of marketing regulation in the U.S.

Are Marketing Restrictions Coming to the U.S. Markets?

New government targets for primary school student attainment have revived the conversation on how we can use pedagogical strategies and teaching methods to improve outcomes for learners. 

A pedagogical approach is at the core of the International Baccalaureate’s Primary Years Programme (PYP), a student-centric approach to education for children aged four to 11. The inquiry-based, transdisciplinary framework builds conceptual learning and delivers excellent outcomes by providing an education that is engaging, relevant, challenging, and significant. 

Learn more at our free webinar
At 1pm (GMT) on Thursday 16 March, join Education Today and the IB to:
• Learn about pedagogy and the PYP
• Understand how the programme complements the Ofsted framework 
• Hear from school leaders sharing their experiences of how implementing the PYP has improved student outcomes.

Read more about the Primary Years Programme: https://www.ibo.org/programmes/primary-years-programme/

Speakers:

• Jane Tipple, Principal, Bearsted Primary Academy: Jane has delivered both the National Curriculum and the IB PYP in two different academies, which are both authorized IB World Schools and have received successful Ofsted inspections under the new framework. She is passionate about the aspirations, philosophy, and ethos of the IB and its values and the significant impact on learning that the programmes have on all students.

• Peter Fidczuk, Development and Recognition Manager, International Baccalaureate UK and Ireland: Peter supports schools interested in developing IB programmes, engages with UK and Irish universities to develop their understanding of the IB and is the point of contact between the IB and the English Department of Education.

How can primary schools take a pedagogical approach to improvement?

Clinical trials don’t happen in a vacuum – they are often a significant undertaking that require people to integrate new routines and procedures into their existing lives, potentially for several years. Understanding, supporting and measuring the participant experience is therefore critical to designing studies that minimise stress and burden, reduce drop-out, and create a positive feedback loop for future programmes.  

 In this webinar Langland will speak to Jonathan Moshinsky, Co-Founder and CEO of Stitch, a technology start-up supporting participant retention by enabling in-study feedback, and Sofia Fionda, Co-Founder of Boxee Group, a healthcare specialist market research agency with expertise in uncovering what motivates people to take part in trials. Join us to explore the why, how and what of improving the clinical experience for participants, sites, and sponsors.

Improving the Clinical Trial Experience: Why, How, and What?

Global clinical trials are a vital component of pharma R&D. Utilizing sites in multiple countries not only provides increased access to eligible and diverse patients - and therefore more robust data - but also promotes health equity and research and innovation across continents.

Another benefit of global clinical trials is the potential for these studies to be completed more quickly and efficiently [1]. However, around four in five clinical trials fail to meet their patient recruitment deadlines [2], which delays patient access to innovative new therapeutics and can prove costly to Sponsors.

Just as treatments are becoming more personalized, so should clinical trial patient recruitment strategies. A ‘one size fits all’ approach to enrollment fails to consider how factors such as an individual country’s culture, healthcare structure and patients’ needs can affect a site’s ability to recruit eligible participants. The key to patient enrollment success is to ‘think local’, even for global studies.

In this webinar, we will:
Discuss the benefits of using a diversified patient recruitment approach for each country within a global study
Investigate how patient recruitment strategies can differ from country to country, 
Hear from two in-country patient recruitment specialists about the challenges relevant to their regions and how they work with sites to overcome these
Share how Innovative Trials’ ‘boots-on-the-ground’ approach in more than 70 countries around the world can help accelerate patient recruitment and retention for your clinical trials.

Speakers:

Georgia Harding - Patient Recruitment Manager, Innovative Trials - georgia.hardy@innovativetrials.co.uk
Nicole Yingst - Strategist, Pfizer - Nicole.Yingst@pfizer.com
Barbara OrlosKaminska- Clinica Enrolment Manager (Poland), Innovative Trials - barbara.orloskaminska@innovativetrials.co.uk
Speaker 4: TBC

Patient Recruitment: Think Global, Act Local

To remain relevant in today’s rapidly changing, information-intense world, regulators must continually evaluate existing market conditions while considering the potential implications of external forces and advances that weigh in on how their markets operate. Featuring a distinguished panel of North American regulators who daily address complex issues like data privacy and cyber security threats to the rapidly growing digital gaming products, financial crime threats like money laundering, fraud and suspicious financial activity, and whether local or national advertising restrictions are warranted to minimize harm amid extensive player acquisition efforts, attempting to streamline the multi-jurisdictional compliance challenges that operators and suppliers face might seem a low priority but is a constant suggestion from the industry. Our panelists will begin by discussing the many challenges facing the industry as we start a new year and share their thoughts on the feasibility of building consensus toward streamlining the regulatory and licensing process.

Regulator Roundtable: regulating in a rapidly evolving world

Over the last few years, a long-running debate has been taking place about what are the appropriate approaches to assessment for today’s world and, since the conventional assessment of GCSEs and A levels was suspended during COVID-19, this debate has intensified with calls to replace GCSEs.  

Additionally, the pandemic accelerated the development of the digital classroom, and so, digital, or e-Assessments, are now on the horizon. Just what this will look like is open to question. For instance, AQA’s trial of digital GCSEs is exploring adaptive – or ‘smart’ – assessments that adjust in difficulty as students progress through the test. The International Baccalaureate (IB) has been assessing learning digitally since 2016 in its curriculum for 11 – 16 year olds, the Middle Years Programme (MYP), and has taken an alternative approach which utilises the full potential of the digital environment to assess knowledge and skills and to enhance learning in the classroom through a positive ‘backwash’ effect. 

Following the IB’s presentation at the ‘Next generation assessment – planning for the future’, (which is being held on the 17 Jan 2023  a conference sponsored by the ASCL, HMC and other organisations), we would like to invite you to learn more about the MYP and the IB’s approach to digital assessment. 

Join our free webinar at 1pm (GMT) on Thursday 26 January in partnership with the IB to learn more.

The International Baccalaureate® (IB) Middle Years Programme (MYP) is for students aged 11-16. Read more about the programme: Middle Years Programme (MYP) - International Baccalaureate® (ibo.org)

At 1pm (GMT) on Thursday 26 January, join Education Today and the IB to:
·    Learn about the MYP
·    Discover the MYP’s flexibility and its innovative digital summative assessments -  eAssessment
·    Understand how the programme complements the Ofsted framework
·    Hear two contrasting schools share their perspectives on implementing the MYP and eAssessments

Moving towards eAssessment with the Middle Years Programme (MYP)

With Tufts reporting that the average number of patient dropouts for clinical trials remains near 30%,  it is clear that there is still much to be done towards improving retention¹.

One of the biggest drivers in keeping patients enrolled is the consent process. Traditional informed consent forms are frequently cited as confusing, leaving patients unsure of what their trial will require of them².

In order to improve the process, we must meet patients on their own terms and find new ways to educate and engage them. At Medable, we use our Patient Advisory Council (PAC) to review our own clinical trial technology and best practices, helping ensure patients leave the consent process truly informed.

Join Medable and key PAC members as we discuss common challenges faced by patients looking to participate in clinical trials. We will explore how a patient-first approach to informed consent can improve patient education, engagement, and comprehension, ultimately improving retention. Attendees will learn about:
1. The challenges of understanding consent information
2. Ideas on how to design the ICF and patient consent process to be patient-centric
3. Considerations in offering the choice of in-person or remote consent
4. Best practices in incorporating technology to increase engagement and comprehension
*Sources:

¹Applied Clinical Trials. Can Recruitment and Retention Get Any Worse? Dec 2019. Ken Getz
²Advarra. Retention in Clinical Trials: Keeping Patients on Protocols. Mar 2021.

Patient Perspectives to Improve Retention with eConsent

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Patient Perspectives to Improve Retention with eConsent

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