This HRSA RCORP RCOE program is supported by the Health Resources & Services Administration (HRSA) of the US Department of Health & Human Services (HHS) as part of an award of $3.33M in the current year with 0% financed with non-governmental sources.

The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement by HRSA, HHS or the US Government.

As the Rural Communities Opioid Response Program (RCORP)-Rural Center of Excellence on SUD Prevention, UR Medicine Recovery Center of Excellence provides access to a wide range of resources on relevant topics. Inclusion in this document does not imply endorsement of, or agreement with, the contents by UR Medicine Recovery Center of Excellence or HRSA.

Privacy and Anonymity

People who use these applications Break the Vape, RITCH, RITCH CBT ("app") may receive an ID number to protect their privacy. Their names are not collected at any point. When research related to this application is completed, participants receive a subject ID number on assessments and study questionnaires. When this research is discussed or published, no one will know that the specific people who used this app were in the study.

De-identified data may also be shared with other researchers around the world or with a publicly available data archive. In such cases, we remove any potentially identifiable information from the data that would indicate any connection to participants.

HIPAA Compliance

A federal government rule has been issued to protect the privacy rights of patients. This rule was issued under a law called the Health Insurance Portability and Accountability Act of 1996 (HIPAA). This rule is designed to protect the confidentiality of personal health information. Personal health information is information about you that could be used to find out who a person is. For research studies related to this application, this includes information collected during the study.

Data Usage and Authorization

This Data Privacy Statement explains how personal health information will be used and who it will be given to ("disclosed") for research studies. It also describes privacy rights, including people's right to see their own personal health information.

By signing the consent document for studies related to this application, people will give permission ("authorization") for the uses and disclosures of de-identified personal health information that are described in this Data Privacy Statement. If people who use this application do not want to allow these uses, they should not use this application.

If individuals agree to participate in research studies related to this application, their personal health information will be used and disclosed in the following ways:

• The investigator will use the information collected during the study to conduct the study.
• Study data that does not directly identify them may be published in medical journals or shared with others as part of scientific discussions.
• Their de-identified study data may be held and processed on computers.

Cancellation and Withdrawal

People who use this application may cancel their authorization at any time by providing written notice to the investigator. If they cancel their authorization, the investigator will no longer use or disclose their study data in connection with this study, unless the study investigator needs to use or disclose personal health information to preserve the scientific integrity of the study.

If individuals cancel their authorization, they will no longer be able to participate in studies associated with this application. However, if they decide to cancel their authorization and withdraw from the study, they will not be penalized or lose any benefits to which they are otherwise entitled.