Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:43 PM
Ignite Modification Date:
2025-12-24 @ 11:43 PM
NCT ID:
NCT06708351
Eligibility Criteria:
Inclusion Criteria:
* AIM 1 (PATIENTS): Aged 25-49 years
* AIM 1 (PATIENTS): Female
* AIM 1 (PATIENTS): Willing to participate in a 90-minute audio-recorded focus group discussion (FGD) and
* AIM 1 (PATIENTS): Speak English or Swahili
* AIM 1 (NURSES, CLINICAL STAFF, ADMINISTRATORS): Aged 18 years or older
* AIM 1 (NURSES, CLINICAL STAFF, ADMINISTRATORS): Involved in implementing intervention components
* AIM 1 (STAKEHOLDERS): Adults (aged \>= 18 years) who are healthcare system users, support persons, healthcare providers and administrators, representatives of the government, professional associations, and non-governmental and faith-based organizations
* AIMS 2 AND 3 (CLINIC PROVIDERS): Aged 18 years and older involved in CC screening, triage, and treatment
* AIMS 2 AND 3 (WOMEN LIVING WITH HIV): Ages 25-49 years
Exclusion Criteria:
* AIM 1: Stakeholder Advisory Board (SAB) members who are not engaged in CC work, individuals who have recently retired from the selected clinics, and patients who are attending the clinic for the first time will be excluded from the study
* AIMS 2 AND 3 (WOMEN LIVING WITH HIV): Pregnant women, women =\< 6 weeks postpartum, and women already confirmed to have cervical cancer will be excluded
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
25 Years
Maximum Age:
49 Years
Study:
NCT06708351
Study Brief:
Protocol Section:
NCT06708351