Drop-In Sessions
Tufts CTSI REDCap “Drop-In” Session

Interested in getting help with your REDCap projects? Tufts CTSI now offers free REDCap Drop-In Sessions on Tuesdays from 10:00AM-noon. Sessions are 30 minutes long and are available to all staff and faculty at Tufts CTSI partner and collaborator organizations.

Schedule a drop-in session to discuss any aspect of REDCap that requires expert advice, such as requesting a feature demonstration, making small modifications to a database, or discussing the pros and cons of different database setups. Drop-in sessions are private, so you can discuss real projects and data; they can be either one-on-one or include multiple members of your study team.

Sign up for a REDCap Drop-In Session HERE

After we receive your request, we will send you a Zoom link for the session.

If you have any questions about drop-in sessions or general questions about REDCap, please email informatics@tuftsctsi.org. For an in-depth consultation, please submit a service request by visiting at Tufts CTSI website and following the “Submit a Request” button.

Conferences & Symposia
8th Annual Asian Health Symposium: “Equity-Centered Data: Making Communities Visible”

*To translate this page, please click here*

*若要查看此活動頁面的中文版本,請點擊此處*

Equity-Centered Data: Making Communities Visible

Register now to join Tufts CTSI and the Addressing Disparities in Asian Populations through Translational Research (ADAPT) Coalition for the 8th Annual Asian Health Symposium Equity-Centered Data: Making Communities Visible.

This half-day, in-person event will be held Tuesday, October 8, 2024 from 8:30AM-1:30PM EST on the Tufts Health Sciences Campus. (Breakfast and Registration: 8:30AM-9:15AM; Lunch and Networking: 12:30PM-1:30PM.)

Asian American and Pacific Islander (AA&PI) populations are the fastest growing racial group in the U.S., comprising over 50 ethnicities speaking more than 100 languages. Despite their diverse lived experiences and health needs, AA&PI communities are often misrepresented as a homogenous “model minority” in health data and research. In August 2023, Massachusetts passed the Data Equity Bill, a landmark legislation mandating state agencies to collect data on major ethnic groups, not just race. This disaggregation of data provides a more accurate and nuanced understanding of diverse communities across the state. While this bill is a significant step towards improving data equity, further efforts are needed across government and health sectors to ensure that all communities are fairly represented in data and decision-making.

Join us to explore the importance of data equity, the vital role of community voices and intersectionality, and cross-sectoral and cross-racial strategies to promote data equity in Massachusetts.

Learning Objectives:

  • Summarize the recently passed Massachusetts Data Equity Bill, its impact on existing public health systems, and its implications for advancing health equity across diverse communities.
  • Discuss the importance of uplifting diverse data sources, intersectionality, and community-led approaches to knowledge production.
  • Identify opportunities for cross-sectoral and cross-racial strategies to promote equitable representation of diverse communities in data collection and knowledge production.

Details

Tuesday, October 8, 2024, 8:30AM-1:30PM EST
Tufts University School of Medicine, Room #114 | 145 Harrison Ave. — Chinatown, Boston

Flyer

Download and share the English language version and translated version!

To visit the translated version of this event page, please click here.

Registration

Researchers and community members are encouraged to attend.

Chinese (Mandarin and Cantonese) language interpretation will also be available for attendees.

Space is limited! Please register here by Tuesday, October 1.

Speaker Biographies

Our keynote speaker will be Akil Vohra, JD. As Director of Policy for AAPI Data, Mr. Vohra oversees federal and state strategies to ensure collection, analysis, publication, and utilization of data to advance understanding and support of Asian American, Native Hawaiian, and Pacific Islander (AANHPI) communities.

Our panel will feature multidisciplinary experts in data equity, including representatives from community-based organizations, government, research institutions, and healthcare systems.

Click here for full biographies of all panelists and speakers!

Agenda

8:30 – 9:15

Registration and Breakfast

                       

9:15 – 9:30

Welcome and Opening Remarks

Harry Selker, Dean, Tufts CTSI

Erin Gibson, Executive Director, Tufts CTSI

MyDzung Chu, ADAPT Director, Tufts CTSI

Dawn Sauma, ADAPT Co-Chair; Co-Executive Director, Asian Task Force Against Domestic Violence (ATASK)

 

9:30 – 10:00

Keynote

Akil Vohra, Director of Policy, AAPI Data

 

10:00 – 11:00

Panel: The Data Equity Movement – Gaps and Opportunities

Co-moderators: Carolyn Chou, Executive Director, Homes for All Massachusetts; Tsung Mou, Assistant Professor, Tufts University School of Medicine

Jenny Chiang, Senior Vice President of Community Engagement and Market Growth, Tufts Medicine Integrated Network

Cheryl Clark, Executive Director and Senior Vice President, Massachusetts League of Community Health Centers’ Institute for Health Equity Research, Evaluation and Policy; Associate Chief for Equity Research and Strategic Partnerships, Division of General Internal Medicine and Primary Care, Brigham and Women’s Hospital

Robert Goldstein, Commissioner, Massachusetts Department of Public Health

Bethany Li, Legal Director, Asian American Legal Defense and Education Fund

Paul Watanabe, Director, Institute for Asian American Studies at the University of Massachusetts Boston

 

11:00 – 11:15

Break and Transition to Breakout Rooms

 

11:15 – 12:15

Concurrent Breakout Rooms

Facilitators: Jaya Aiyer, Director, Asian and Pacific Islanders Civic Action Network; Catherine Chung, Senior Program Manager, Asian Women for Health; Tsung Mou, Assistant Professor, Tufts University School of Medicine

Group 1: Intersectionality and Structural Drivers of Health

Intersectionality recognizes the multiple identities we hold and the unique challenges individuals face as a result of intersecting and overlapping discrimination. This breakout will explore how we can build research and data systems that capture intersectionality and structural drivers of health.

                         

Group 2: Centering Community Voices

Community stories are vital to understanding the impacts and causes of local issues. This breakout will explore the importance of diverse data – including community stories – and how we can center communities in our data and our ways of producing knowledge.

 

Group 3: Cross-Racial Strategies for Data Equity

Data equity is a cross-racial issue, affecting diverse communities across the state. This breakout will discuss strategies for cross-racial solidarity to further health equity and to ensure that data equity benefits all communities.

 

Reconvene and report-out

 

12:20 – 12:30

Summary and Closing Remarks

MyDzung Chu, ADAPT Director, Tufts CTSI

 

12:30 – 1:30

Lunch and Networking

 

Thank you to our Symposium planning committee (Dawn Sauma, ADAPT Co-Chair and Co-Executive Director, Asian Task Force Against Domestic Violence; Naheed Esar, Executive Director, Asian Women for Health; and Tsung Mou, Assistant Professor, Tufts University School of Medicine), as well as our Tufts CTSI Professional Education team and Communications Manager, for all of their work on this event.

This event is provided free of charge, and was supported by the National Center for Advancing Translational Sciences, National Institutes of health, Award Number UM1TR004398. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

Conferences & Symposia
“以公平為數據的中心:讓社區更清晰可見”

*To translate this page, please click here*

*若要查看此活動頁面的中文版本,請點擊此處*

以公平為數據的中心:讓社區更清晰可見

 

立即註冊,加入塔夫茨 CTSI 和透過轉化研究解決亞裔人口差異聯盟 (ADAPT),參加第八屆年度亞裔健康研討會 – “以公平為數據的中心:讓社區更清晰可見”。

這半天的活動將於美東時間 10 月 8 日(星期二)上午 8:30 分 至下午 1:30分 在塔夫茨健康科學學院舉行。 (早餐和登記:8:30AM-9:15AM 午餐和社交:12:30PM-1:30PM。)

亞裔和太平洋島民 (AA&PI) 是美國成長最快的種族群體,由 50 多個種族組成,講 100 多種語言。儘管 AA&PI 社群的生活經驗和健康需求各不相同,但在健康數據和研究中,他們經常被誤認為是同質的「模範少數族裔」。 2023 年 8 月,馬薩諸塞州通過了《數據公平法案》,這是一項具有里程碑意義的立法,要求痲州機構收集主要族裔群體的數據,而不僅是種族的數據。這種數據分類可以讓人們更準確、更細緻地了解全州不同的社區。雖然該法案是提高數據公平性的重要一步,但政府和衛生部門仍需要進一步努力,以確保所有社區在數據和決策中得到公平的代表。

 

與我們一起探討數據公平的重要性、社區聲音和跨種族策略的重要作用,以及促進馬薩諸塞州數據公平的跨領域和跨種族戰略。

 

學習目標:

  • 總結最近通過的馬薩諸塞州數據公平法案、其對現有公共衛生系統的影響及其對促進不同社區健康公平的影響。
  • 討論提升多樣化資料來源、交叉性和以社區為主導的知識收集方法的重要性。
  • 瞭解跨部門和跨種族策略的機會,以促進不同社區在資料收集和知識收集方面的公平代表性。

 

活動細節

美東時間 2024 年 10 月 8 日(星期二)上午 8:30分 至下午 1:30分

塔夫茨大學醫學院

醫學教育中心–波士頓唐人街 夏利臣街145 號 #114室

(Center for Medical Education, Room #114 | 145 Harrison Ave. — Chinatown, Boston)

 

傳單

下載並分享英文版中文版傳單!

若要查看此活動頁面的中文版本,請點擊此處

 

報名注冊

我們鼓勵研究人員和社區成員參加。

也將為參與者提供中文(國語和廣東話)翻譯。

位置有限!請於 10 月 1 日之前在此報名註冊

 

演講嘉賓簡介

我們的主講人是法學博士 Akil Vohra (阿基爾·沃赫拉) 。身為AAPI 數據政策主任,Vohra (沃赫拉) 先生負責監督聯邦和州戰略,以確保資料的收集、分析、發布和使用,以增進對美國亞裔、夏威夷原住民和太平洋島民(AANHPI) 社區的理解和支持。

我們的小組將由數據公平方面的多學科專家組成,包括來自社區組織、政府、研究機構和醫療健保系統的代表。

 

 

研討會 議程

8:30 – 9:15 報名及早餐

 

9:15 – 9:30 歡迎致開幕詞

Harry Selker,塔夫茨 CTSI 院長

Erin Gibson,塔夫茨 CTSI 執行董事

MyDzung Chu,塔夫茨 CTSI ADAPT 總監

Dawn Sauma,ADAPT 共同主席;亞裔反家庭暴力小組 (ATASK) 聯合執行董事

 

9:30 – 10:00 主題演講

Akil Vohra,政策主任,AAPI 數據

 

10:00 – 11:00 小組討論:以公平為數據的中心:讓社區更清晰可見

 

11:00 – 11:15 休息並轉移至分組討論室

 

11:15 – 12:15 分組討論

第一組:健康的交叉性和結構性驅動因素

 

交叉性的認識到我們擁有的多重身分,以及個人因交叉和重疊歧視而面臨的獨特挑戰。本次小組討論將探討我們如何建立研究和數據系統,來找到健康的交叉性和結構性驅動因素。

第二組:獲得社區聲音為中心

 

社區故事對於了解當地問題的影響和原因至關重要。本次小組討論將探討多樣化數據(包括社區故事)的重要性,以及我們如何以數據信息收集方式為中心。

第三組:數據公平的跨種族策略

 

數據公平是一個跨種族問題,影響著全州不同的社區。本小組討論將探討跨種族團結的策略,進一步以促進健康公平,並確保數據公平及受惠給所有社區。

  回到大組匯報

 

12:20 – 12:30 總結與結束語

MyDzung Chu,塔夫茨 CTSI ADAPT 主任

 

12:30 – 1:30 午餐與交流

 

感謝我們的研討會策劃委員會(ADAPT 共同主席,亞裔反家庭暴力工作小組共同執行董事 Dawn Sauma;亞裔婦女健康協會執行董事 Naheed Esar;塔夫茨大學醫學院助理教授 Tsung Mou)。以及我們的塔夫茨CTSI 專業教育團隊和外展經理,感謝他們為本次活動所做的所有工作。

活動是免費提供,並獲得美國國立衛生研究院國家轉化科學促進中心的支持,獎項編號 UM1TR004398。內容完全由作者負責,不一定代表 NIH 的官方觀點。

Seminars & Workshops
“Unlocking Insights: The Power of Natural Language Processing in Healthcare” with Dr. Alysse Wurcel

Join us for an engaging live Zoom event featuring Dr. Alysse Wurcel, a dedicated clinical scientist and thought leader whose work in translational science showcases the power of Natural Language Processing (NLP) to unlock information hidden in clinical data.

Dr. Wurcel’s NLP research identifies a difficult to uncover population – people who use drugs – and demonstrates the limitations of traditional Electronic Medical Record searches. Her work reveals how NLP can serve as a more effective, efficient, and ethical alternative to chart reviews. By incorporating NLP in her research, Dr. Wurcel not only identifies patients more accurately but creates the opportunity to improve care through earlier identification of at-risk populations in need of better access to care and services.

Why attend?

– Learn from Experts: Gain insights from Dr. Wurcel and our expert panelists on how NLP is transforming clinical and translational research. Understand how it serves as a bridge between raw data and tangible healthcare improvements.

– Build Strong Collaborative Teams: Explore the vital role of interdisciplinary collaboration in translational science. Learn how partnering with the right experts can strengthen your team and accelerate your research and clinical goals.

Explore Ethical and Practical Dimensions: Dive into the ethical considerations and challenges of implementing NLP in healthcare settings. Understand the importance of language choices and how they can influence patient trust, engagement, and outcomes.

– Innovate in Patient Care: Engage with thought leaders about the future of patient care. Learn how adopting cutting-edge technologies like NLP can create more person-centered healthcare systems and contribute to a broader understanding of patient needs.

Utilize the Translational Science Benefits Model: Analyze this case example to identify the wide-ranging benefits of your research, highlighting how these advantages impact interest holders across various disciplines.

Who should attend?

– Researchers and Scientists interested in identifying and understanding the needs of patients who use drugs, exploring the applications of NLP, or identifying additional benefits of their research using the Translational Science Benefits Model.

– Clinicians and Healthcare Providers seeking to enhance patient care through innovative technologies and learn how to integrate NLP into clinical practice.

– Informatics Specialists and Data Scientists passionate about data-driven healthcare solutions and their practical implementation.

– Ethics and Language Experts interested in the intersection of language, technology, and patient care, focusing on the ethical implications of these advancements.

– Program Administrators and Grant Managers responsible for designing and overseeing small funding opportunities aimed at advancing translational science.

Expert panelists

Laura Haaber Ihle, PhD (AI Ethicist)

Aurora Quaye, MD (Anesthesiologist and researcher)

Liz Scharnetzki, PhD (Social Psychologist)

Annika Schoene, PhD (Computer Scientist)

Lightning talks

Leslie Rideout, PhD, FNP, BSN (Tufts Medical Center)

Aurora Quaye, MD (Maine Health)

Isha Agarwal, MD, ScD (Maine Health)

Details

Live session via Zoom: Thursday, October 24, 10:00AM-11:30AM EST

Registration

Register in advance.

Contact

For any questions about the event, please contact Alyssa Cabrera.