Adyar cancer institute
Chennai, Tamil Nadu, 600020, India
NCT Number: NCT06874985
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.
Looking for future studies?
Notify Me30 year–59 year
All sexes
Interventional
Not applicable
Chennai, Tamil Nadu, 600020, India
The Access Cancer Care India (ACCI) project is aimed at designing and evaluating an evidence-based multi-level strategy tailored to the local health system to enhance access to early detection and care continuum for oral, breast, and cervical cancers among rural populations in India, who are socioeconomically disadvantaged and vulnerable to huge inequity in cancer care.
Pre-intervention phase:
The pre-intervention assessment was conducted in four blocks (Vanur, Mailam, Vikravandi, Kanai) in Viluppuram District, Tamil Nadu, between August 2023 and July 2024 to understand the barriers and challenges rural men and women face in accessing cancer early detection care continuum using various methods.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants in the selected villages will be shown a two-minute video developed specifically for the Lived Experience Communication Campaign in addition to usual awareness they receive for cancer screening mobilisation. The video will feature personal narratives from cancer survivors and local leaders emphasizing the importance of early detection and screening.
Time frame: 1 month after the participation
The proportion of eligible participants who visited a healthcare center for cervical, breast, or oral cancer screening within one month of the intervention (or usual care in the control group).
Time frame: 6 months
The proportion of eligible individuals living in the intervention and control villages covered through invitations for cancer screening.
Time frame: 6 months
The proportion of individuals eligible for screening who participated in the screening program.
Time frame: 6 months
The proportion of individuals who participated in the cancer screening program requiring further assessment.
Time frame: 6 months
The proportion of individuals eligible for screening who are diagnosed with cancers.
Time frame: 6 months
The proportion of individuals eligible for screening who are referred for treatment to higher centres.
Time frame: 6 months
Proportion of eligible men and women who received the intervention.
Time frame: 6 months
Proportion of eligible men and women who agreed to participate in the existing cancer screening program.
Time frame: 6 months
Proportion of eligible men and women who find the intervention (Lived experience campaign video) to be acceptable.
International Agency for Research on Cancer
Other
Effectiveness and Impact of the Lived Experience Cancer Awareness Campaign on Participation in the Existing Cancer Screening Programs [Oral, Breast and Cervical] Among the Rural Population in Villupuram District, Tamil Nadu
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06910657
Adenocarcinoma, Adnexal Diseases
St Louis, Missouri, United States
View Trial DetailsNCT07038369
Adnexal Diseases, Advanced Solid Tumors
Los Angeles, California, United States
View Trial DetailsNCT06628388
Anxiety, Anxiety Disorders
Hong Kong, HONG KONG
View Trial DetailsNCT06647992
Behavior, Cervical Cancers
Istanbul, Üsküdar, Turkey (Türkiye)
View Trial Details