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Study reference: NCT07212465. HopeStage can help you review the study, but cannot decide medical eligibility.
RecruitingNCT07212465
Accelerated Neuromodulation of Anterior Cingulate Cortex for Depression
This study is recruiting. It focuses on depression and currently lists participation information in Canada.
DepressionDeviceFrom 60 Years to 85 Years
Key information made simple
This study is comparing Active Brainsway H7-Coil Deep TMS System with 20-40 sessions of sham stimulation for people with depression. Participants receive Active Brainsway H7-Coil Deep TMS System or 20-40 sessions of sham stimulation and complete study visits and assessments. Some participants may receive 20-40 sessions of sham stimulation instead of the study treatment, and direct benefit is not guaranteed.
Your next step
The official record suggests in-person participation through a clinic, with sites including Rotman Research Institute at Baycrest in Toronto. Participation appears to involve a study treatment together with follow-up visits and routine safety or progress checks. 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 active substance or alcohol problems that could affect the results 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
- Sponsor
- Rotman Research Institute at Baycrest
- Sponsor type
- Research institute
- Main activity
- brain stimulation
- Intervention
- Not available
- Time commitment
- long follow-up or multiple visits
- Study phase
- Not available
- Enrollment
- Not available
- Recruitment status
- Recruiting
- Source
- Official registry link
Key study information
- Official title
- Accelerated Neuromodulation of Anterior Cingulate Cortex for Depression
- Condition
- Major Depressive Disorder (MDD)
- Study status
- Recruiting
- Sponsor / lead affiliation
- Rotman Research Institute at Baycrest
- Location / country
- Canada
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT07212465
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 Canada.
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
- Accelerated Neuromodulation of Anterior Cingulate Cortex for Depression
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT07212465
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 Accelerated Neuromodulation of Anterior Cingulate Cortex for 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 Rotman Research Institute at Baycrest. Based on the sponsor name or official registry information, it appears to be a research institute. 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 long follow-up or multiple visits. 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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