ObjectiveTo describe our experience of screening with visual inspection with acetic acid (VIA) and colposcopy to identify women with highâgrade precancerous cervical lesions who were candidates for cryotherapy. Women were screened to determine eligibility for a clinical trial testing the safety and efficacy of a new, simple and inexpensive cryotherapy device (CryoPopÂź) targeted for use in low and middleâincome countries (LMICs).DesignProspective cohort study.SettingPrimary and urban health centres in Belagavi, Hubballi and Vijayapur, India.PopulationWomen in the ageâgroup 30â49âyears, premenopausal, with no prior hysterectomy and no known HIV infection were eligible for screening.MethodsVisual inspection with acetic acid was performed on eligible women following informed consent. VIAâpositive women were referred for colposcopy and biopsy. Biopsies were read by two pathologists independently, with a third pathologist acting as tieâbreaker if needed.Main outcome measuresThe primary outcome measures were the number/proportion of women screening positive by VIA and the number/proportion of those women screening VIAâpositive found to have highâgrade cervical lesions on biopsy (cervical intraepithelial neoplasia 2/3 [CIN 2/3]). Demographic variables were compared between women who screened VIAâpositive and those who screened VIAânegative; a separate comparison of demographic and limited reproductive variables was performed between women who had CIN 2/3 on biopsy and those without CIN 2/3 on biopsy. Chiâsquare or Fisher's exact tests for categorical data and tâtests or analysis of variance for numeric data were used with all tests twoâsided and performed at an alpha 0.05 level of statistical significance.ResultsA total of 9130 women were screened with VIA between 4 July 2020 and 31 March 2021. The mean age of all women screened was 37âyears (standard deviationâ=â5.6âyears) with 6073 of the women (66.5%) in the 30â39âyear range. Only 1% of women reported prior cervical cancer screening. A total of 501 women (5.5%) were VIAâpositive; of these, 401 women underwent colposcopy. Of those who had colposcopy, 17 (4.2%) had highâgrade lesions on biopsy, an additional 164 (40.9%) had lowâgrade cervical lesions on biopsy or endocervical curettage and one woman (0.2%) was found to have invasive cancer. VIAâpositive women were younger and had higher levels of education and income; however, women who were VIAâpositive and found to have CINâ2/3 were older, were more likely to be housewives and had higher household income than those without CINâ2/3.ConclusionDespite the COVIDâ19 pandemic, over 9100 women were screened with VIA for precancerous lesions. However, only 17 (4.2%) were found to have biopsyâproven highâgrade cervical lesions, underscoring the subjective performance of VIA as a screening method. Given that this is significantly lower than rates reported in the literature, it is possible that the prevalence of highâgrade lesions in this population was impacted by screening a younger and more rural population. This study demonstrates that screening is feasible in an organised fashion and can be scaled up rapidly. However, while inexpensive and allowing for sameâday treatment, VIA may be too subjective and have insufficient accuracy clearly to identify lesions requiring treatment, particularly in lowâprevalence and lowârisk populations, calling into question its overall costâeffectiveness.