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core competencies iconCompetencies & Principles

Core Competencies for All Health Professionals (2007)

This document provides basic guidance to a broad range of individuals and groups as they plan educational initiatives in genetics, genomics, and genetically based health care.

Target Audience: All health care professionals

Core Principles in Family History for all health professionals (2011)

This document lays out health care professional competencies for taking and interpreting a family history. There is a complementary slide set on family history for teaching purposes available.

Target Audience: All health care professionals

CORE PRINCIPLES IN GENETICS (2004)

This document provides guidance about the content that should constitute basic instruction in genetics and genomics for those in health care. The principles focus on basic biology related to genetics. They are available in English and Spanish

Target Audience: All health care professionals

PRINCIPLES OF GENETICS IN THE CONTEXT OF COMMON DISEASE (2006)

NCHPEG developed a set of principles that are intended to guide educational efforts that address the expansion of genetics and genomics into the realm of common complex diseases. The principles were adapted from: “A Framework for Genetics and Complex Disease,” with permission of the Foundation for Genetic Education and Counseling

Target Audience: Educators


target iconTargeted Education Programs & Discipline-Specific Programs

The goal of each Web-based program is to increase genomcis literacy among faculty and practitioners within a specific health-professional audience. The content is case driven and uses interactive exercises to reinforce key genetics concepts within the clinical context of the targeted discipline.

Read more about NCHPEG's Targeted Education Programs>>

ABCs of Chromosomal Microarray (2013)new icon

This is a web-based resource for developmental and behavioral pediatricians on indications for and interpretation of chromosomal microarray (CMA). This program was developed in collaboration between NCHPEG and the International Collaboration for Clinical Genomics (ICCG). 

Target audience: Developmental and Behavioral Pediatricians 

Genomics for Child Neurology (2013) new icon

The core of this program is a comprehensive curriculum that educators can use to implement local workshops for child nuerology providers. Clinicians can use the web-based materials, which include interactive case studies and point of care tools, to build skills and reinforce concepts from the workshops. Topics include genomic risk assessment, genetic and genomic testing, and communication with families about genomic data. This program was developed in collaboration with the Children's National Medical Center. 

Target audience:  Child Neurology Educators and Clinicians

Colorectal Cancer: Is Your Patient at High Risk? (2012)

This web-based educational program designed to improve the primary care provider’s ability to identify hereditary colorectal cancer syndromes in their patients. This program focuses on case-based learning through a series of clinical scenarios that apply point-of-care tools to key clinical roles in risk assessment, genetic testing, communication, and management.

Target Audience: Primary Care Providers

Genetics and Social Science: Expanding Transdisciplinary Research (2011)

This web-based educational program with the aim of providing sufficient genetics and genomics background to allow social and behavioral scientists to engage effectively in interdisciplinary research with genetics researchers. The overarching goal of this project is to create an educational program that will improve social scientists’ genetics literacy in the following areas: conversation, imagination, evaluation, and integration.

Target Audience: Social and Behavioral Scientist Researchers

Nutrition and Genetics: Key concepts and clinical scenarios for Dietetic educators and practitioners in the US & UK (2008)

This web-based program focuses on genetic and genomic concepts as it relates to the practice of dietitians and nutritionists. Along with the basic genetics content on family history, genetic/genomic testing, and other topics, this program discusses evaluating genetics and genomics studies, including assessing the clinical utility and validity of genetic changes related to common disease. The interactive case studies discuss MTHFR, MCAD, cystic fibrosis, and celiac disease. CEUs will be available through the American Dietician Association (ADA). NCHPEG developed this targeted education program in conjunction with ADA, the British Dietetics Association, and the National Genetics and Development Centre (Birmingham, U.K.). This work was supported by the National Human Genome Research Institute, Health Resources and Services Administration, and the Office of Rare Disease, National Institutes of Health.

Target Audience: Dietitians and Nutritionists

Genetics in the Physician Assistant’s Practice (2007)

This web-based program focuses on genetics in the physican assistant’s practice. It contains information about basic genetics concepts relevant to clinical practice (e.g., taking a family history and genetic testing), teaching tools, resources, and interactive case studies. The case studies discuss fragile X syndrome, factor V Leiden, and familal hypercholesterolemia. CMEs are available through the American Academy of Physician Assistants (AAPA). NCHPEG developed this targeted education program in conjunction with AAPA. This work was supported by the National Human Genome Research Institute, Health Resources and Services Administration, and the Office of Rare Disease, National Institutes of Health.

Target Audience: Physician Assistants

Genetics in the Practice of Speech-Language Pathology and Audiology (2006)

This web-based program focuses on genetic contributions to speech, language, and hearing. It contains information about basic genetics concepts relevant to clinical practice (e.g., taking a family history and genetic testing), teaching tools, resources, and interactive case studies. The case studies discuss connexin 26, Stickler syndrome, and DiGeorge syndrome. CEUs are available through the American Academy of Audiology and American Speech-Language-Hearing Association (ASHA). NCHPEG developed this targeted education program in conjunction with ASHA, National Society of Genetic Counselors, and the University of Cincinnati. This work was supported by the National Human Genome Research Institute, Health Resources and Services Administration, and the Office of Rare Disease, National Institutes of Health.

Target Audience: Speech-Language Pathologists and Audiologists

Genetics and Common Disorders: Implications for Primary Care and Public Health Providers (2005)

This program focuses on the genetics of common disease and on the broad principles that emerge when viewing disease from the perspectives of variation and individuality - which are at the heart of thinking genetically. The content includes discussion of principles of genetics in common disorders, incorporating family history into practice, ethical, legal, and social implications, and applying genomics to prevention and management. It also includes two interactive case studies: thrombophilia and colorectal cancer. This work was supported by the U.S. Department of Energy.

This program is not currently available in a web format. We hope to make the program available on the web soon. We have a limited number of CD-ROM hard copies available. Please contact us to request a copy of the CD-ROM, as supplies last. Include "Request for CD" in the title of your email. Thank you for your patience.

NCHPEG

Target Audience: Primary Care Providers and Public Health Professionals

Genetics, Disease, and Dentistry (2004)

This web-based program focuses on genetics in the dental practice. It contains information about basic genetics concepts relevant to clinical practice (e.g., definition of genes and mutation and taking a family history), resources, and case studies. The case studies discuss Gorlin syndrome (nevoid basal cell carcinoma syndrome), diabetes, and osteogenesis imperfecta. NCHPEG developed this targeted education program in conjunction with American Dental Hygienists Association and National Institute of Dental and Craniofacial Research.

Target Audience: Dentists and Dental Hygienists

Genetics Is Relevant Now: Nurses' views and patients' stories

NCHPEG and the Department of Nursing at the University of Cincinnati developed this Web-based educational program that illustrates current genetics applications in nursing practice. Specifically, the content addresses the relevance of genetics in infectious disease, oncology nursing, and common disease. It includes audio clips from genetics nursing experts and from patients.

Target Audience: Nurses

Genetics and Major Psychiatric Disorders: A Program for Genetic Counselors (2002)

This program is intended to provide an introduction to psychiatric genetics, with a focus on the genetics of common complex disease, for genetics professionals. The content includes discussion of complex disease, overview of psychiatry, research in psychiatric genetics, unipolar depression, bipolar disorder, schizophrenia, and issues in psychiatric genetic counseling. This work was supported by the U.S. Department of Energy.

Target Audience: Genetics Professionals

 


Educational Aids

The following resources are relevant for educators who are developing lectures or teaching genetics content to students and health professionals.

CASE STUDY CATALOG

This resource provides direct access to case studies and clinical scenarios that address over 20 different clinical conditions including common and rare disorders. The Catalog describes the key components and learning goals of each case as well as suggestions for appropriate healthcare provider audiences.

CRITICAL ASSESSMENT OF INFORMATION

The Trust It or Trash It? program provides a guide to help individuals think critically about the quality of educational materials. This project, supported by CDC with the Genetic Alliance as the lead agency, strives to provide tools to help families and non-geneticist health providers develop and assess educational materials for Duchenne and Becker muscular dystrophy and fragile X syndrome.

FAMILY HISTORY

Almost all of NCHPEG's programs emphasize the importance of family history collection and application to patient care.  This section links to the many different family history educational resources within the NCHPEG network.

GENERAL GENETICS

This section links to some of the basic genetics content that is part of all of our programs, including information about genetic testing.

GENOMIC EDUCATION DEVELOPMENT GUIDE

This guide can be used to create effective materials that are targeted to the specific audience and focused on key messages.

PSYCHIATRIC GENETICS

These resources provide an introduction to psychiatric genetics, with a focus on the genetics of common complex disease. The content includes discussion of complex disease, overview of psychiatry, research in psychiatric genetics, unipolar depression, bipolar disorder, schizophrenia, and issues in psychiatric genetic counseling.

RACE & GENETICS FAQ

The FAQ was developed as a complement to a 90 minute CME session on Race & Genetics.  In additional to learning from the FAQ, you can request a copy of the DVD recording or you can watch it now.  The FAQ contains information on genetic variation between populations, genetic variation in disease, biology and race, and population research involving different racial and ethnic groups. The Robert Wood Johnson Foundation provided the funding for this program.


tools iconPoint of Care Tools

Point of Care Tools are for immediate use in the clinical setting.  NCHPEG is committed to creating additional Point of Care Tools to improve access to and effectiveness of genetics education for the busy clinician.  We have a number of projects currently in development, such as GeneFacts.  Have ideas for new Point of Care Tools?  Contact us and let us know!

Colorectal Cancer Resources

This section has quick links for tools and resources on hereditary colorectal cancer syndromes.  There are tools for risk assessment, genetic testing, communication and collaboration, and screening and surveillance.  There are also fact sheets on Lynch syndrome, familial adenomatous polyposis, MYH-associated colorectal cancer, and familial colorectal cancer.  These are part of the larger program "Colorectal Cancer: Is Your Patient at High Risk?".

Family History Collection & Assessment

Click here for quick resources on family history collect and risk assessment, including guidelines on genetic red flags and risk stratification.

Genetic Information Nondiscrimination Act (GINA)

This program is a discussion guide for clinicians.  It includes background documents, a guide suggesting how and when to talk about GINA with patients, a teaching slide set, and case studies that describe how the law works in a variety of real-world, clinical settings.

Non-Invasive Prenatal Test (NIPT) Factsheet

This fact sheet is a resource for prenatal care providers.  It reviews NIPT technology, indications, detection rates, accuracy and other considerations; provides guidance around genetic counseling for these tests; and outlines points to consider and questions to ask when choosing a testing laboratory.

Psychiatric Disease Resources

This section has quick links for general information about psychiatric disease and genetics, recurrence risks in a family, and a script for asking questions about mental illness. There resources are part of the larger Genetics and Major Psychiatric Disorders program.

Risk Communication

Risk communication is a complex process that is essential for effective risk assessment.  This fact sheet is a quick reference on risk communication tips, with links for more detailed information on risk communication.

 


newsletter iconNewsletters

NCHPEG produces newsletters periodically throughout the year. Initially, these newsletters focused on topics in family history. Currently, each newsletter considers a single topic from different perspectives. Recent newsletter topics have included

 

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