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Intervention Study on Mental Health and Screening Behaviors Among HPV-Positive Women in Low Health Resource Areas in China

Intervention Study on Mental Health and Screening Behaviors Among HPV-Positive Women in Low Health Resource Areas in China: Based on the Cognitive Behavioral Therapy (CBT) Model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111320
Enrollment
Unknown
Registered
2025-10-29
Start date
2025-10-29
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

HPV infection

Interventions

Intervention group:The intervention group will receive a psychological intervention based on the Cognitive Behavioral Therapy (CBT) framework via the "Yi Ban Sui Xing" WeChat mini-program. Co-designed
Control group:The control group will receive usual care provided by the local county and township health system, which may include result notification, distribution of health education materials, and

Sponsors

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. Women aged between 35-64 years. 2. Received a positive HPV screening result within the past month and currently do not require immediate treatment for high-grade lesions (e.g., cytology results showing no HSIL or worse, or colposcopy findings excluding high-grade lesions). 3. Women who are able to use a smartphone or tablet, and are willing and able to use the WeChat mini-program. 4. Women with basic reading comprehension and smartphone operation skills, who are able to independently complete electronic questionnaires with appropriate guidance. 5. Women who are willing to participate.

Exclusion criteria

Exclusion criteria: 1. Patients with a confirmed diagnosis of cervical cancer or other gynecological malignancies. 2. Women with a severe mental illness or cognitive impairment that prevents them from completing the questionnaires and intervention. 3. Women who are currently pregnant. 4. Women who are currently participating in or have previously participated in a similar research study.

Design outcomes

Primary

MeasureTime frame
Anxiety;Screening adherence;

Secondary

MeasureTime frame
Stigma;Screening intention;HPV infection clearance rate;

Countries

China

Contacts

Public ContactQiao Youlin

Chinese Academy of Medical Sciences & Peking Union Medical College

qiaoy@cicams.ac.cn+86 188 1171 9259

Outcome results

None listed

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