Introduction:
Welcome! Thank you for your interest in our survey! What follows is some information about this project that will give you the context you need to decide if you’d like to participate. Participation in this study is entirely voluntary and you can refuse to participate in, or opt out of the survey, at any time without penalty.
What is this survey about & why is it being done?
This survey is being conducted to gain insights into non-romantic, non-sexual, committed relationships of all kinds and how these relationships influence loneliness, social support, and belonging. The information gathered will be used as background for a book about the full spectrum of these kinds of relationships. Answers shared in this survey will be compiled into statistical data and used only in aggregate. No individual data will be published, with one possible exception: you will have the opportunity at the end of this survey to answer open-ended questions that give you the opportunity to share your thoughts more directly. These are entirely optional, however if you choose to share your thoughts here, some of your words might be included in the final manuscript.
What Will I Do and How Long Will It Take?
This is an online survey with 53 questions and should only take about 20 minutes to complete. You can opt out at any time. If you do? Your survey will be discarded and the answers you previously completed will not be used.
What are the Possible Benefits of participating in this survey?
Direct Benefits for you as a participant: There are no direct benefits to you for participating.
Indirect Benefits: The information you contribute about your experiences will also increase our overall understanding of deeply committed, non-romantic and/or non-sexual relationships: how they form, what they look like, and how the partners can be supported by their families, their communities, and their mental and medical health providers.
What are the risks and discomforts of participating in this survey?
The risks to participating in this survey are similar to risks encountered in everyday life. These include:
1) Some questions may be personal or distressing. You do not need to answer any questions that do not want to answer.
2) Limitations to privacy:
o Everyone working on this project is committed to maintaining the privacy of our participants as fully as possible and will not share your information with anyone outside of the research team.
o The research team are mandatory reporters. This means that disclosures of ongoing child abuse, elder abuse, intentional transmission of communicable diseases, or threats of harm to self or others must be reported to the appropriate resources.
3) Possible loss of confidentiality: there is a chance your data could be seen by someone who shouldn’t have access to it. We’re minimizing this risk in the following ways:
o We are using a GDRP compliant survey platform.
o No personally identifying information (name, phone number, email, birthday, etc.) will be collected.
o Information that could be theoretically identifiable (age, sex, gender, etc.) will be aggregated into generalized statistical data.
o All survey data will be stored on a password-protected, encrypted cloud-based server.
o No IP addresses will be collected to further promote anonymity.
o Participants who chose to answer the optional, open-answer questions may reach out at any time and request to have their answers deleted from our survey.