Cancer Urological and Genital Diseases cervical cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women of 25 years Never had cervical cancer screening Attending the general female outpatient clinic at Thika Level 5 hospital Consents for the study. Own a mobile phone and consent to receive communication through their mobile phones during the study period.
Exclusion criteria
Exclusion criteria: Women who are not attending the general outpatient clinic Those that do not give consent Those with overt cancer of cervix or high grade squamus intraepithelial lesion (HSIL) Those below the age of 25 years Women with previous hysterectomies, Those who do not own a mobile phones Those who have been screened for cervical cancer before. Patients who are too sick and need hospital admission and those with vaginal bleeding will also be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be defined as study subjects with normal Pap test at beseline who complete a repeat Pap test at 12 months from baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. Women with low grade lesion who return for re-screening at 6 months;1. Women who comply with recommendation of repeat Pap test after 12 months | — |
Countries
Kenya
Contacts
Senior lecturer and Phd student