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Evaluating the Impact of Digital Health Interventions on Cervical Cancer Screening KAP in Health-Resource-Limited Areas

Evaluating the Impact of Digital Health Interventions on Cervical Cancer Screening KAP in Health-Resource-Limited Areas

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100545
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-10
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

Cervical cancer

Interventions

Intervention group 1:Precise digital health interventions for women with screening and digital health interventions for screening doctors
Intervention group 2:Extensive digital health interventions for women with screening and digital health interventions for screening doctors

Sponsors

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for women with cervical cancer screening: women aged 35-64; No history of cervical disease; intact cervix; No history of surgery for cervical cancer and precancerous lesions; It is clear that no cervical cancer screening has been received in the past 3 years; Be in good health and be able to be screened for cervical cancer; Understand the project procedures, voluntarily participate, and sign the informed consent form. 2. Inclusion criteria for cervical cancer screening doctors: undertake local cervical cancer screening and have the ability to carry out colposcopy; The infrastructure conditions of the unit meet the requirements for the construction of a digital screening platform for cervical cancer; Understand the project procedures, voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Women who do not meet the age; previous history of cervical cancer; no complete cervix; previous history of surgery for cervical cancer or cervical precancerous lesions; menstrual period, pregnant women; the vaginal use of drugs within 3 days affected the test results; physically or psychologically unable to participate in cervical cancer screening or unable to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Digital-service acceptance rate;Awareness score;Attitude score;Referral rate;Referral interval;

Secondary

MeasureTime frame
Awareness rate;Intention to referral;Click-through rate;Click-through time;Message-reading time;Treatment rate;

Countries

China

Contacts

Public ContactYoulin Qiao

School of Population Medicine and Public Health, Chinese Academy of Medical Sciences & Peking Union Medical College

qiaoy@cicams.ac.cn+86 186 7971 9756

Outcome results

None listed

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