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A study to improve knowledge and awareness about cervical and breast cancer through educational sessions for young adults and women in India

CAPTURE: Cancer Awareness and screening Promotion Through Utilization of community Resources and their Empowerment. - CAPTURE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092632
Enrollment
2785
Registered
2025-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Educational intervention to promote cervical and breast cancer awareness in community. Comparator-Not applicable: A Health behaviour theory based educational intervention designed based

Sponsors

University of Luxembourg
Lead Sponsor
Dr Jyoshma Dsouza
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Cross sectional Survey in community(Phase 1): Men and women in general population and in university college, Physically and mentally healthy, able to provide consent, knows local language will be include in the participation in survey. The survey will assess knowledge , general beliefs and attitude towards health related practices and choices, knowledge about cancer and cancer screening. PHASE2-Educational Intervention (in community): An educational intervention will target women aged 30-60 years though community organizations that provide consent. Women will be invited through announcements. Those illing to voluntarily participate will be included. Phase 2-Educational intervention (in university college):This phase will invite students(males and females) to participate in cancer awareness intervention. Those willing to participate will be included in the study. Educational intervention in (hospital settings): Women aged 30-60 years attending hopsitals for reasons will be approached by trained Nursing students and those willing to participate, know the language, provide consent will be included. Assessing cancer delay diagnosis: Individuals admitted or attending hospital, diagnosed with cervical or breast cancer will be approached and consent will be obtained. Those willing to participate will be included to collect information through a interviewer administered survey. Participants will be included irrespective of age.

Exclusion criteria

Exclusion criteria: Individuals physically or mentally challenged, those unable to provide consent, or in terminal stage with palliative care will not be included.

Design outcomes

Primary

MeasureTime frame
1. At least 60% of participants in the intervention group will demonstrate an improvement in knowledge scores from baseline to post-intervention. Timepoint: T0 Baseline: Before the intervention (for knowledge, beliefs, and attitudes) T1 Immediately Post-Intervention: After the intervention (to assess improvement in knowledge and attitude using post-test form)

Secondary

MeasureTime frame
2. Atleast 50% women attending the awareness campaign will voluntarily seek screening for breast and cervical cancer.Timepoint: T2 Follow-up at 3 and 6 Months Post-Intervention: To assess number of actual screening uptake among participants who received screening awareness with handouts/pamphlets.

Countries

India

Contacts

Public ContactJyotsna Coelho

University of Luxembourg

jyoshma.dsouza@uni.lu621760721

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026