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Community feedback indicated privacy as a major concern especially regarding perceptions of non-participants, and that community acceptability required thorough explanation of study tools and procedures.
After receiving an explanation of study procedures and aims and questions were answered, participants provided written informed consent to participate.
At this second visit, participants received a detailed explanation of study procedures, signed or marked a consent form for enrollment, received HIV counseling, provided urine for pregnancy testing, provided another OMT sample for HIV testing, and if eligible were randomized to receive either SAVVY or placebo.
After explanation of study procedures and written informed consent, a structured questionnaire was administered to interview the participants and collect their sociodemographic information as well as sexual and reproductive history (sexual behaviors, obstetric history, menstrual history, past history of STI) and medical history relevant to HIV/AIDS and cervical cancer.
After explanation of study, informed consent was obtained from all participants.
If they were interested, eligibility was assessed and a full explanation of study involvement was provided.
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After explanations of study procedures to leaders and community members, few questions were asked about export of samples or the archiving of samples for future research.
Parents will then receive a detailed explanation of the study and be offered study participation.
An explanation of the study was given to each study candidate.
All subjects gave written informed consent to participate in the study after a detailed explanation of the study procedures.
Only a subsection of reviewed studies offered sufficiently detailed explanation of the study approach and respective results.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com