None listed
Conditions
Interventions
Intervention1: NIL: NIL
Sponsors
Dr Sharmila Pimple
Eligibility
Inclusion criteria
Inclusion criteria: Women between the age group of 25-60 years, Non-pregnant With an intact uterus and, No past history of cervical neoplasia.
Exclusion criteria
Exclusion criteria: Unmarried Have had a total hysterectomy Have a history of cervical cancer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of eligible women aware of cervical cancer screening programs. Percentage of eligible women screened using hrHPV self-sampling. Percentage of hrHPV-positive women adhering to follow-up recommendations Percentage of women receiving appropriate treatment following cervical cancer screening. Operational Feasibility: Coverage of self-sample HPV/DNA screening among the target population. Number and percentage of invalid test results. Compliance rates of screen-positive cases undergoing reference diagnostic procedures: Conventional cytology. Colposcopy-guided biopsy or Endocervical Curettage (ECC). Technical Feasibility: Duration from sample collection to laboratory transport. Duration from sample collection to report delivery.Timepoint: 24 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| To identify the sociocultural barriers, preferences, and facilitators influencing the adoption of HPV self-sampling among under-screened tribal women in Maharashtra. To evaluate the acceptability of HPV self-sampling as a screening method in the tribal population. To assess the operational feasibility of implementing HPV self-sampling as a screening strategy.Timepoint: 24 months. | — |
Countries
India
Contacts
Public ContactDr Sharmila Pimple
Tata Memorial Hospital
Outcome results
None listed