A Study on the Application of Positive Psychological Counseling Based on "Dou Bao" Software in Patients With Post-stroke Depression
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: The positive psychological counseling platform of the "Doubao" software.
- Who it may be relevant to
- Registry conditions: Stroke, Post Stroke Depression. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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
- Other The positive psychological counseling platform of the "Doubao" software
Utilize an active psychological counseling platform based on the "Doubao" software
Primary outcome measures
- Depression assessment [Time frame: Before the intervention and 3 months after the intervention]
Secondary outcome measures (3)
- appraisal of life quality [Time frame: Before the intervention and 3 months after the intervention]
- the satisfaction of patients [Time frame: 3 months after the intervention]
- Research dropout rate [Time frame: 3 months after the intervention]
Eligibility criteria
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;
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07336888 · KY-2025-303