Effectiveness and Impact of the Lived Experience Cancer Awareness Campaign on Screening Participa… (NCT06874985) | Clinical Trial Compass
CompletedNot Applicable
Effectiveness and Impact of the Lived Experience Cancer Awareness Campaign on Screening Participation
India1,264 participantsStarted 2025-05-05
Plain-language summary
This study will be conducted as a parallel-arm, open-label, randomized controlled trial (RCT) to evaluate the effectiveness and impact of the Lived Experience Communication Campaign (LECC) on cancer screening participation rates \[oral, breast and cervical cancer\] compared to the usual standard awareness campaign across selected rural population in Villupuram district, Tamil Nadu.
Who can participate
Age range
30 Years – 59 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Men and women aged 30-59 years
* No prior diagnosis of cervical, breast, or oral cancer.
* Have not undergone screening for the above cancers in the last 1 year
* Provide informed consent to participate
Exclusion Criteria:
* Individuals with a previous history of any cancer
* Individuals with severe cognitive impairments that prevent comprehension of study materials
* Participants unwilling to provide informed consent
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Screening Participation Rate
Timeframe: 1 month after the participation
2
Invitation coverage in both arms
Timeframe: 6 months
3
Examination coverage in both arms
Timeframe: 6 months
4
Further assessment coverage in both arm
Timeframe: 6 months
5
Detection of cancers in both arms
Timeframe: 6 months
6
Treatment referral in both arms
Timeframe: 6 months
Trial details
NCT IDNCT06874985
SponsorInternational Agency for Research on Cancer