{"id":4894,"date":"2019-10-28T13:30:12","date_gmt":"2019-10-28T18:30:12","guid":{"rendered":"https:\/\/calliercenter.utdallas.edu\/?post_type=doc&p=4894"},"modified":"2022-11-10T15:49:50","modified_gmt":"2022-11-10T21:49:50","slug":"section-15-research-uses-and-disclosures-of-phi","status":"publish","type":"doc","link":"https:\/\/calliercenter.utdallas.edu\/doc\/section-15-research-uses-and-disclosures-of-phi\/","title":{"rendered":"Section 15: Research Uses and Disclosures of PHI"},"content":{"rendered":"\n

Section 15: Research Uses and Disclosures of PHI<\/h2>\n\n\n\n

Callier Center PHI can be accessed for research purposes with satisfactory evidence that UT Dallas Internal Review Board (IRB) has approved the research proposal and granted a HIPAA authorization waiver. To access Callier patient information, the Director of Audiology Clinical Services, Director of Speech-Language Pathology Clinical Services, or Cochlear Implant Program Manager will serve as the liaison with the Primary Investigator (PI) or approved IRB member associated with the study and is responsible to report the study to the Executive Director.<\/p>\n\n\n\n

UT Dallas Workforce must follow these procedures to access or use any Callier Center PHI for research of any kind.<\/p>\n\n\n\n

Procedure<\/strong><\/h2>\n\n\n\n

1. <\/strong>Determine That the Requested Use or Disclosure Is for Research Purposes<\/strong><\/h3>\n\n\n\n

This policy only applies when the purpose of the requested use or disclosure is research, defined as a systematic investigation including research development, testing, and evaluation that is designed to develop or contribute to generalizable knowledge. This policy does not apply if the purpose of the requested use or disclosure is health care operations, defined to include quality assessment and improvement activities, including outcomes evaluation and development of clinical guidelines, provided that the obtaining of generalizable knowledge is not the primary purpose of any studies resulting from such activities. This includes population-based activities relating to improving health or reducing health care costs, protocol development, case management and care coordination.<\/p>\n\n\n\n

2. Determine that the Information to be Used or Disclosed Is PHI<\/strong><\/h3>\n\n\n\n

This policy only applies if the information being used for research is PHI. If the information being used or disclosed has been completely de-identified in accordance with Section 16 of this Manual, this policy does not apply.<\/p>\n\n\n\n

3. Initiate Contact with Callier Patients for Purposes of Research Registry Recruitment<\/strong><\/h3>\n\n\n\n

The Director of Clinical Services or Program Manager will be responsible for oversight of all recruitment activities for Callier patients. The PI or approved IRB member associated with the IRB approved study may contact patients who are listed in the clinical research registry. Individual clinic patients may opt out of participation in the research registry by:<\/p>\n\n\n\n