Post Stroke Depression, Stroke
Conditions
Brief summary
Patients with PSD have the characteristics of high incidence rate, difficult identification and great harm. However, the existing AI chat platforms have not developed any relevant software or programs for PSD patients. Given that the chatbot function in the Douba software is relatively mature and can flexibly modify the corresponding intelligent agent according to user needs, this study intends to appropriately supplement and optimize the AI agent in the Douba software to explore the effect of the chatbot in the software in alleviating the symptoms of PSD patients.
Interventions
OTHERThe positive psychological counseling platform of the Doubao software
Utilize an active psychological counseling platform based on the Doubao software
Sponsors
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Meets the criteria of either the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke or the Chinese Guidelines for the Diagnosis and Treatment of Acute Cerebral Hemorrhage and is confirmed by CT or MRI; * Patients with stable vital signs and conditions; * Meets the Third Edition of the Classification and Diagnosis Criteria for Mental Disorders in China and has a score of ≥5 on the 9-item Patient Health Questionnaire (PHQ-9) scale; * Patients are over 18 years old; * Can understand the relevant content of the scale correctly and provide answers independently or with the help of others, have clear consciousness and sign the consent form; * Can use smartphones.
Exclusion criteria
* Those with severe functional impairments of important organs such as the heart, lungs, liver and kidneys; * Those without a smart phone;
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Depression assessment | Before the intervention and 3 months after the intervention | Use the PHQ-9 scale,The sensitivity of this scale in diagnosing depression was 0.82, and the specificity was 0.87. The PHQ-9 scale collects information on the degree to which the evaluated individuals are troubled by different depressive symptoms, including loss of interest, low mood, sleep disorders, feeling tired, changes in appetite, poor self-perception, lack of concentration, slow movements or irritability, and suicidal thoughts. The score for each item ranges from 0 (none at all) to 3 (almost every day), and the total score ranges from 0 to 27. The higher the score, the more severe the symptoms. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| appraisal of life quality | Before the intervention and 3 months after the intervention | The assessment was conducted using the short version of the stroke-specific quality of life scale (SV-SS-QoL). This scale consists of 2 dimensions and 12 items. Each item is scored using the Likert 5-point scale, with values ranging from 1 to 5. The total score ranges from 12 to 60. A higher scale score indicates better quality of life. The Cronbach's α coefficient of this scale is 0.882, the split-half reliability is 0.845, and the test-retest reliability is 0.839. |
| the satisfaction of patients | 3 months after the intervention | Have the patients rate their satisfaction with the psychological counseling method used in this study on a scale of 1 to 5. If they feel extremely dissatisfied, they should give a score of 1; if they are dissatisfied, 2; if they are basically satisfied, 3; if they are moderately satisfied, 4; and if they feel extremely satisfied, 5. For those who give a score of extremely dissatisfied or extremely satisfied, ask them for the specific reasons to prevent them from giving random scores. |
| Research dropout rate | 3 months after the intervention | After comparing the two groups of patients 3 months later, the study withdrawal rates were determined. The study withdrawal rate = the number of people in this group 3 months later / the initial number of people in this group in the study × 100%. |
Outcome results
None listed