IRB Determination

TYPE OF REVIEW – NON HUMAN SUBJECTS RESEARCH DETERMINATION/ETHICAL EVALUATION

Determination
Date:

February 09, 2023

IRB ID:

10755-ELong

Protocol:

Message Evaluation for CDC’s Stop Overdose Campaigns

Sponsor:

Everett L. long

Principal
Investigator:

Everett Long, PHD, MA, BA

Sterling IRB is in receipt of submission materials for the above-referenced study.
Items Reviewed:
•
Exemption or Non-Human Subjects Research Determination Request
•
A1. 75D301-21-F-11264 (1).pdf (Grant Application /or Contract)
•
Attachment 4 - Survey Instrument.docx (Data Collection Form)
•
Consent Form.jpeg (*Participant Information Sheet)
•
DOCR TB2 Stop Overdose Campaigns Evaluation Plan.12-15 (2).docx (Protocol)

Based on the information available to the IRB, the Sterling IRB Chairman (or designee) has determined that this submission does
not constitute human subjects research, and is therefore ineligible for IRB approval. Although it is not within the IRB's jurisdiction
to approve non human subjects research, the IRB Chairman (or designee) has conducted an ethical evaluation of the above referenced study to assess whether any aspect of the study, as submitted, appears to violate any human subject protections.
Following review, the IRB Chairman's (or designee's) assessment of the study is as follows:
The above-referenced study, as submitted to Sterling IRB, does not appear to be in violation of any human subject protections.
This evaluation does not constitute IRB approval of the proposed study.
Sterling IRB's determination that the materials submitted are non human subjects research and its ethical evaluation assessment
are based on the study-related information available to Sterling IRB as of the determination date listed above. Should any changes
be made to the study subsequent to Sterling IRB's determination, the determination noted herein as well as the findings of this
evaluation and are no longer applicable.
As the project applicant you are responsible for following all policies of Sterling IRB as described in the Exemption or Non-Human
Subjects Research Determination Request Submission Agreement which you accepted with project submission. It is your
responsibility to ensure this project is conducted in accordance with applicable regulations (local, state and federal) as well as any
requirements established by the IRB at the time of the review determination. Refer to the Investigator Handbook at
www.sterlingirb.com for details of these responsibilities.
The Board will be apprised of this evaluation.

APP821 NHSR.EthicalEvaluation.Variable Effective Date: 01.05.21 Version: 1.1