None listed
Conditions
Interventions
Intervention1: Innovative health education material: Development of innovative sexual health education materials under the study to engage women and communities to:
(1) Increased HPV self-sampling amo
Sponsors
Fund for Innovation and Transformation ICN Global Affairs Canada
Eligibility
Inclusion criteria
Inclusion criteria: A. Female Participantsâ?? eligibility criteria include: 1.Under or Never screened (UNS) women (i.e. self-report of >4 years since last Pap test/VIA test, including no history of Pap test or VIA test in past). 2.Sexually active women aged 30-69 years. 3.No history of hysterectomy or past history of precancerous or cancerous lesions. 4.Willing to share contact information with the study team. B. Eligibility criteria for men Participants include: Male family members (husbands, fathers, brothers, sons, cousins, friends) identified and referred by UNS women participants shall be above age of 18 years. C. The service providers eligibility criteria for focus group discussion include: Shall be from the villages identified for implementation of the study and having a fair knowledge of cervical cancer screening.
Exclusion criteria
Exclusion criteria: 1. Pregnant women 2. Women with past history of cervical cancer 3. Women who have undergone hysterectomy 4. Individuals not willing to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Quantify the screening outcomes and referrals for diagnostic test 2.Acceptability / Preference outcome for HPV Self sampling kits. 3.Quantifying educational outcomes for knowledge and attitude about cervical cancer risk factors and screening( overall and by gender) in the communityTimepoint: 15 months | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NA | — |
Countries
India
Contacts
Public ContactDr Gauravi Mishra
Tata Memorial Hospital
Outcome results
None listed