Predicting Illness Trajectories In Fully Remitted Major Depression Using Concurrent TBS/fNIRS
This study is active but not recruiting. It focuses on depression and currently lists study information in China.
Key information made simple
This study is looking at whether Theta-burst stimulation (TBS) can help people with Major Depression in Remission or Healthy. Participants take part in Theta-burst stimulation (TBS) and complete follow-up assessments. Some participants may receive Healthy control group instead of the study treatment, and direct benefit is not guaranteed.
Your next step
The official record suggests in-person participation through a university, with sites including The Hong Kong Polytechnic University. 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 meeting the main study requirements, while common reasons not to take part include major medical issues that could make participation unsuitable 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
- Active Not Recruiting
- Sponsor
- The Hong Kong Polytechnic University
- Sponsor type
- University
- Main activity
- medication or study treatment
- Intervention
- Not available
- Source
- Official registry link
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Key study information
- Official title
- Predicting Illness Trajectories In Fully Remitted Major Depression Using Concurrent TBS/fNIRS
- Condition
- Depression, Healthy
- Study status
- Active Not Recruiting
- Sponsor / lead affiliation
- The Hong Kong Polytechnic University
- Location / country
- China
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT05579015
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 give access to a new approach being evaluated.
It requires regular visits and structured follow-up.
Requires travel, with in-person participation in China.
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.
- Official title
- Predicting Illness Trajectories In Fully Remitted Major Depression Using Concurrent TBS/fNIRS
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT05579015
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 Predicting Illness Trajectories In Fully Remitted Major Depression Using Concurrent TBS/fNIRS?
This study is exploring medication or study treatment 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 control group. Direct benefit is not guaranteed.
Who is behind this study, and what type of sponsor is it?
This study is sponsored by The Hong Kong Polytechnic 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 medication or study treatment, 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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