Skip to main content

Table 2 Participant outcomes to be evaluated before and after the HPV-based trial

From: Protocol for the formative phase of a trial (SHE-CAN) to test co-designed implementation strategies for HPV-based cervical screening among vulnerable women in two diverse settings in India

Outcome

Outcome definitions

Current VIA programme

HPV trial

Reach

a) Invitation rate: % invited out of eligible

b) Screening participation rate: % screened out of invited

c) Follow-up rate for assessment: % assessed out of screen positives

d) Treatment rate: % completed treatment for pre-cancer/initiated cancer treatment, out of assessed

e) Representativeness: key differences between invited vs not invited, screened and not screened, followed/treated vs those not followed up/treated

f) Barriers for non-participation

Facility assessment survey checklist

Qualitative study

Screening registry for trial

Qualitative study

Acceptability

a) Acceptability of screening and associated treatment

Qualitative study

Qualitative study

Feedback surveys

Effectiveness

a) Well managed: % of women invited who are screened and receive appropriate treatment and advice

b) Number of pre cancer and cancers detected by screening and by clinical presentation

c) Adverse events of screening among participants including social/economic

d) Any other/unexpected health benefits associated with screening

Facility assessment survey checklist

Qualitative study

Screening registry for trial

Feedback surveys

Qualitative study