TNG Southerners Experiences of Reproductive and Natal Care

Informed Consent

RESEARCH STUDY CONSENT FORM:
You are invited to participate in a research study by Dr. Phoenix Rosewood, PhD., MA, LMHC, of Westfield State University and Dr. Melanie Walsh, PhD, LPC-S, of the University of New Haven. This study has undergone IRB approval from Antioch University Seattle. This form describes the study to help you determine if you are comfortable participating.

CRITERIA FOR PARTICIPATION:
You are invited to participate if you meet the following criteria:
-Participants who are 18 or older
-Identify as transgender, nonbinary, and/or gender-expansive
-Live most of the year (7+ months) in one of the following states: FL, MS, TX, OK, GA, SC, VA, KY, TN, AL, AR, LA, NC, DE, MD, MO, or WV
-Are currently pregnant, have attempted pregnancy, have experienced miscarriage or abortion, or have given birth

If you do not meet these criteria, thank you for your interest. You do not have to proceed further. You may simply close your browser window.
If you do meet these criteria, please continue reading the informed consent form for more information and to participate.

STUDY OVERVIEW AND PROCEDURE:
Researcher Self-reflexivity Statement: Both researchers involved the study are members of the queer community, one identifies as nonbinary and the other identifies as cisgender. Both researchers are white. Both researchers work extensively with gender and sexual minorities in their clinical practices and are providers of gender affirming care. One researcher is located in the Northeast while the other lives and works in the U.S. South.

The purpose of this study is to understand and explore the phenomenon of transgender, nonbinary and gender expansive people navigating access to prenatal, perinatal and postnatal healthcare in the American South and the impact of this pursuit on their mental health. The research question asks, how do people living in the American south experience their attempts at receiving healthcare related to conception, gestation, and birth and how are these processes shaped by intersecting identities, including mental health, geography and their sense of their healthcare provider’s knowledge of gender expansive reproductive healthcare? The goal of this study is to understand barriers, supports, and the impact of current legislation and provider knowledge on TNG people’s health and well-being. Your insights will help inform future reports, presentations, and publications. All data will be de-identified.

Participation involves completing a confidential qualitative interview about your experiences accessing reproductive or pregnancy-related healthcare in the South. If you participate in the study, you will be asked to complete a demographic questionnaire and engage with 8 open-ended questions. The total time commitment for the survey and questionnaire is 20 minutes or longer.
RISKS AND BENEFITS OF PARTICIPATION:
​​No study is completely risk-free. However, we do not anticipate you will be harmed or distressed during this study. You may stop being in the study at any time if you become uncomfortable. Occasionally, people who participate in counseling-oriented research find that they would like to seek out mental health care and/or support. For more information, you may want to contact the National Alliance on Mental Illness (NAMI) at: 1-800-950-NAMI (6263).

You should also be aware that there is a small possibility that unauthorized parties could view responses because it is an online survey (e.g., computer hackers because your responses are being entered and stored on a web server).

In terms of benefits, there are no immediate benefits to you from your participation. However, we may learn more about the topic of focus. In addition, upon completion of the survey, you are eligible to share your email address and electronically receive a $50 Visa gift card for your time.

DATA PRIVACY:
No identifying information will be asked at any time unless you opt-in to provide an email to receive a gift card for participating. Additionally, you may choose to provide an email address for post analysis, member-checking purposes, which will be completed via encrypted email. Otherwise, IP address collection is turned off and your name will not be requested.

YOUR RIGHTS AS A PARTICIPANT:
Your participation in this study is voluntary. You can decide not to be in the study at any time and can simply close the browser window. Only completed surveys will be utilized for data analysis. In addition, it is important for you to know that your decision to participate or not to participate will not affect your relations with Antioch University in any way.

CONTACT INFORMATION:
This study has been approved by the Antioch University Institutional Review Board (IRB). If you have ethical concerns about this study or your treatment as a participant, you may contact the chair of the IRB (Dr. Jenkins - kjenkins@antioch.edu) or the researcher.
Lead Researcher: Phoenix Rosewood, Ph.D., MA, LMHC
Email: prosewood@westfield.ma.edu
Research Advisor: Dr. Stephanie Thorson-Olesen
Email: sthorsonolesen@antioch.edu

If you have questions about or do not understand something in this form, please contact the faculty researcher for additional information. Do not click “next” unless the researcher has answered your questions and you decide that you want to be part of this study.

CONSENT TO PARTICIPATION:
By clicking “next” you agree to the following statements:
I have read this form, and I have been able to ask questions about this study.
I have not given up my legal rights as a research participant.
I fit the criteria to participate in this study.
I voluntarily agree to be in this study.
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