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Prediction model construction of mental health problems in patients with cervical cancer and precancerous lesions based on artificial intelligence algorithm and evaluation of effect of online psychological comprehensive intervention

Prediction model construction of mental health problems in patients with cervical cancer and precancerous lesions based on artificial intelligence algorithm and evaluation of effect of online psychological comprehensive intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087926
Enrollment
Unknown
Registered
2024-08-07
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Depression and anxiety

Interventions

intervention group:Online mindfulness + positive psychotherapy + aromatherapy combined intervention
Online mindfulness intervention group:Online mindfulness intervention
control group:Distribution of common science materials of mental health
Anxiety Identification Group:Accept standardized diagnosis of depression or anxiety from a psychiatrist and complete questionnaire, EEG, and rs-fMRI data collection
Depression Identification Group:Accept standardized diagnosis of depression from a psychiatrist and complete questionnaire, EEG, and rs-fMRI data collection

Sponsors

Shenzhen Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age 18 and above (2) Patients who have been definitively diagnosed by a clinician as cervical cancer or precancerous lesions; (3) Can independently cooperate with various scale assessments, EEG and rs-fMRI collection; (4) No longer receive any other treatment for cervical cancer and precancerous lesions during the study period; (5) There is a mobile phone that can be connected to the Internet at any time and the Bluetooth function of the mobile phone is normal; (6) Right-handed; (7) I give informed consent to the whole process, and sign the electronic informed consent as required by the Ethics Committee.

Exclusion criteria

Exclusion criteria: (1) There are conditions that are not suitable for EEG and rs-fMRI collection, such as obvious scar on the forehead skin or cardiac pacemaker or artificial heart valve in the body; (2) Suffering from serious heart, brain, lung, kidney, liver and other internal diseases or other inappropriate to participate in the study; (3) Persons who are unable to cooperate with the investigation or intervention; (4) Researchers who are involved in other health promotion or clinical interventions. Those who meet any of the above criteria are excluded.

Design outcomes

Primary

MeasureTime frame
Electroencephalogram ;rs-fMRI;anxiety symptoms;symptoms of depression;

Secondary

MeasureTime frame
quality of life;Resilience;mindfulness;perceived social support;sleep quality;fatigue;acceptance of intervention materials;

Countries

China

Contacts

Public Contactwangyueyun

Shenzhen Maternal and Child Health Care Hospital

wangyueyun@126.com+86 139 2371 2005

Outcome results

None listed

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