Intervention Study of Virtual Reality-Based Mindfulness-Based Cognitive Therapy (VR-MBCT) Combined With Adaptive tDCS Modulation for Post-Stroke Depression
This study is not yet recruiting. It focuses on depression and currently lists study information in Global.
Key information made simple
This study is comparing Virtual Reality Mindfulness-Based Cognitive Therapy (Active VR-MBCT) with VR-MBCT Control Group (Active VR-MBCT + Sham tDCS) for people with Post-stroke Depression. Participants receive Virtual Reality Mindfulness-Based Cognitive Therapy (Active VR-MBCT) or VR-MBCT Control Group (Active VR-MBCT + Sham tDCS) and complete study visits and assessments. Some participants may receive VR-MBCT Control Group (Active VR-MBCT + Sham tDCS) instead of the study treatment, and direct benefit is not guaranteed.
Your next step
The official record suggests a remote format run through a clinic. Participation appears to involve assessments along with scans or samples to help researchers understand patterns more clearly. The main fit is usually matching the main diagnosis and being able to understand the study and consent, while common reasons not to take part include safety concerns that need urgent care first and pregnancy or breastfeeding. The official record does not list a formal phase, which usually means this is focused more on feasibility, delivery, or support than a standard drug-development stage.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
- Time commitment
- multiple visits or assessments
- Study phase
- Not available
- Enrollment
- Not available
- Recruitment status
- Not Yet Recruiting
- Sponsor
- Second Affiliated Hospital, School of Medicine, Zhejiang University
- Sponsor type
- University
- Main activity
- brain stimulation
- Intervention
- Not available
- Source
- Official registry link
Want help reviewing this study?
Key study information
- Condition
- Depression
- Study status
- Not Yet Recruiting
- Sponsor / lead affiliation
- Second Affiliated Hospital, School of Medicine, Zhejiang University
- Location / country
- Global
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT07422740
Why this study may matter
This study may matter because it adds public evidence around depression. HopeStage presents it as a starting point for understanding the study, checking the official source, and preparing questions with a care team.
For you
Taking part may help clarify how this condition is measured or understood.
It requires regular visits and structured follow-up.
Can be done remotely.
Registry reference
This page links back to the public source record so people can verify details directly with the registry and research team.
If you want the full study description, eligibility criteria, locations, and sponsor information in the original format, this is the place to check before taking the next step.
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT07422740
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is Intervention Study of Virtual Reality-Based Mindfulness-Based Cognitive Therapy (VR-MBCT) Combined With Adaptive tDCS Modulation for Post-Stroke Depression?
This study is exploring brain stimulation for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. It includes a comparison with a sham comparison. Direct benefit is not guaranteed.
Who is behind this study, and what type of sponsor is it?
This study is sponsored by Second Affiliated Hospital, School of Medicine, Zhejiang University. Based on the sponsor name or official registry information, it appears to be a university. You should verify the details in the official registry record.
What does participation involve, what phase is it, and what should I ask about safety?
This study may involve brain stimulation, study visits, and assessments. The time commitment is multiple visits or assessments. The study phase is not available in HopeStage data. Check the official source record to see whether a phase is listed. Enrollment is not available in HopeStage data. HopeStage cannot say whether a study is safe or right for you. Before joining, ask the research team about possible risks, time commitment, visits, side effects, compensation, safety monitoring, and whether participation may affect your current care.
Where can I verify the study details?
Use the official source record linked on this page to check the full study description, recruitment status, eligibility criteria, locations, sponsor information, phase, enrollment, contact details, and any listed risks or requirements.
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