Depression and anxiety
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time frame |
|---|---|
| Electroencephalogram ;rs-fMRI;anxiety symptoms;symptoms of depression; | — |
Secondary
| Measure | Time frame |
|---|---|
| quality of life;Resilience;mindfulness;perceived social support;sleep quality;fatigue;acceptance of intervention materials; | — |
Countries
China
Contacts
Shenzhen Maternal and Child Health Care Hospital