Patient-oriented Pragmatic Feasibility study with RTMS in Depression and Anxiety
This study is recruiting in Canada. It focuses on depression.
Key information made simple
This study is looking at whether questionnaires and follow-up can help people with Major Depressive Episode or depression. Participants take part in questionnaires and follow-up and complete follow-up assessments. Taking part may give some people access to questionnaires and follow-up, but direct benefit is not guaranteed.
Your next step
The official record suggests in-person participation through a lab, with sites including Non-Invasive Neurostimulation Therapies (NINET) Laboratory, UBC Department of Psychiatry in Vancouver. Participation appears to involve questionnaires, interviews, or regular check-ins about day-to-day experience. The main fit is usually being able to understand the study and consent and meeting the main study requirements, 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
- Recruiting
- Sponsor
- University of British Columbia
- Sponsor type
- University
- Main activity
- medication or study treatment
- Intervention
- Not available
- Source
- Official registry link
Want help reviewing this study?
Key study information
- Official title
- Patient-oriented Randomized Pragmatic Feasibility Trial with RTMS in Depression and Anxiety
- Condition
- Depression, Anxiety
- Study status
- Recruiting
- Sponsor / lead affiliation
- University of British Columbia
- Location / country
- Canada
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT05028738
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 follow-up, often through questionnaires or interviews.
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
- Patient-oriented Randomized Pragmatic Feasibility Trial with RTMS in Depression and Anxiety
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT05028738
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 Patient-oriented Pragmatic Feasibility study with RTMS in Depression and Anxiety?
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. Direct benefit is not guaranteed.
Who is behind this study, and what type of sponsor is it?
This study is sponsored by University of British Columbia. 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.
Want to find a study that may fit you better?
Answer a few simple questions to explore HopeStage studies by condition, country, and situation.
Find a study that may fit me
