CompletedNCT05577481

Neuronavigation Guided iTBS With Personalized Target for Depression

This study is completed. It focuses on depression and currently lists study information in China.

DepressionOtherFrom 18 Years to 60 Years

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Study reference: NCT05577481. HopeStage can help you review the study, but cannot decide medical eligibility.

In plain English

Key information made simple

This study is looking at whether sham iTBS combined with antidepressants can help people with Depression. Participants take part in sham iTBS combined with antidepressants and complete follow-up assessments. Some participants may receive functional MRI-guided iTBS(sham group) instead of the study treatment, and direct benefit is not guaranteed.

What to expect

Your next step

The official record suggests in-person participation through a research setting, with sites including XijingH in Xi'an. 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, while common reasons not to take part include active substance or alcohol problems that could affect the results and major medical issues that could make participation unsuitable. This is an early-stage study, which usually means a smaller group and a focus on learning how the approach behaves.

Before joining

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?

Study clarity

Things to check before joining

Study start dateStarted: July 10, 2023

Time commitment: multiple visits or assessments
Study phase: Not available
Enrollment: Not available
Recruitment status: Completed
Sponsor: Xijing Hospital
Sponsor type: Hospital / academic medical center
Main activity: observational follow-up
Intervention: Not available
Source: Official registry link

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Public study data

Key study information

Official title: Neuronavigation Guided iTBS With Personalized Target for Depression
Condition: Depression
Study status: Completed
Sponsor / lead affiliation: Xijing Hospital
Location / country: China
Registry: ClinicalTrials.gov
External trial ID: NCT05577481

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.

In practice

For you

Taking part may help clarify how this condition is measured or understood.

It requires regular visits and structured follow-up.

Requires travel, with in-person participation in China.

Official source

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: Neuronavigation Guided iTBS With Personalized Target for Depression
Source: ClinicalTrials.gov
Official registry link: Open official registry
External trial ID: NCT05577481

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is Neuronavigation Guided iTBS With Personalized Target for Depression?

This study is exploring observational follow-up 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 Xijing Hospital. Based on the sponsor name or official registry information, it appears to be a hospital or academic medical center. 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 observational follow-up, 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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