About this trial
To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
stakeholder advisory board members;
patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial;
patients and community members participating in formative research activities;
providers, clinic staff, and other health system stakeholders from partnering health systems;
Disqualifiers
Report being currently pregnant
History of total hysterectomy
History of cervical cancer
Trial design
Single group
Treatments tested in this trial
HR-HPV Testing
BehavioralGiven by Interview and focus groups
Treatment groups
Trial outcomes
Primary outcomes
Safety and Adverse Events (AEs). Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 4.03
Sponsors and contacts
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