Recruitment & eligibility

CL Catherine Leiner
TC Tamara Cody
NM Nathan Mullins
MR Melinda Ramage
BO Bayla M. M. Ostrach
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The researchers had access to eligible participants at the invitation of the program directors, who asked for the research to be conducted so that they could eventually learn more about their buprenorphine patients’ experiences seeking and receiving care. All potentially eligible participants were approached with information about the study and participants identified as eligible based on the inclusion criteria (patient sample: over 18, diagnosed with perinatal OUD, treated with buprenorphine) were specifically invited to participate in semi-structured interviews and/or a focus group. All patients attending the program during the study period were also informed and consented about participant-observation ongoing in the clinic and offered the option to decline to be observed with no negative consequences for their receipt of care.

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