None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Those women who will be willing to give consent will be recruited to participate in the study. • Those will be able to read and understand the Odia language.
Exclusion criteria
Exclusion criteria: • Those will not be available during data collection. • Those having a past history of cervical cancer.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome could be measured by the percentage increase in women undergoing cervical cancer screening tests (e.g., Pap smear, HPV testing, VIA) before and after the intervention.Timepoint: At 2month,4month,6month,12 month | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Measure the increase in knowledge and awareness about cervical cancer and its prevention among the target population through pre- and post-intervention surveys. 2. Evaluate the acceptance and satisfaction levels of the different screening methods among women using questionnaires and feedback forms. 3. Assess changes in health-seeking behaviour, such as regular visits for cervical health check-ups, through follow-up surveys. 4. Identify and measure the reduction in barriers (e.g., cultural, financial, logistical) that women face in accessing cervical cancer screening services. Timepoint: At 2month,4month,6month,12 month | — |
Countries
India
Contacts
SUM NURSING COLLEGE, SOA, DEEMED TO BE UNIVERSITY