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Study reference: NCT05516095. HopeStage can help you review the study, but cannot decide medical eligibility.
CompletedNCT05516095
The Antidepressant Effect of Intermittent Theta Burst Stimulation (iTBS)
This study is completed. It focuses on depression and currently lists study information in Norway.
DepressionOtherFrom 22 Years to 65 Years
Key information made simple
This study exists to compare options and see whether questionnaires and follow-up reports offers something meaningfully different. Researchers are trying to understand whether questionnaires and follow-up reports can improve attention, thinking, or day-to-day functioning. For people living with Depression, the gap between what sounds good on paper and what works in daily life is often important. If the findings are useful, they could help future care become more targeted, practical, and easier to trust. Taking part helps build the evidence that can improve understanding and care for others over time.
Your next step
The official record suggests in-person participation through a hospital, with sites including University Hospital North Norway in Tromsø. 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 active substance or alcohol problems that could affect the results and major medical issues that could make participation unsuitable. 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
- University Hospital of North Norway
- Sponsor type
- Hospital / academic medical center
- Main activity
- brain stimulation
- Intervention
- Not available
- Time commitment
- long follow-up or multiple visits
- Study phase
- Not available
- Enrollment
- Not available
- Recruitment status
- Completed
- Source
- Official registry link
Key study information
- Official title
- The Antidepressant Effect of Intermittent Theta Burst Stimulation (iTBS)
- Condition
- Depression; Executive Dysfunction
- Study status
- Completed
- Sponsor / lead affiliation
- University Hospital of North Norway
- Location / country
- Norway
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT05516095
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 improve understanding of your condition.
It requires regular follow-up, often through questionnaires or interviews.
Requires travel, with in-person participation in Norway.
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
- The Antidepressant Effect of Intermittent Theta Burst Stimulation (iTBS)
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT05516095
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 The Antidepressant Effect of Intermittent Theta Burst Stimulation (iTBS)?
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. Direct benefit is not guaranteed.
Who is behind this study, and what type of sponsor is it?
This study is sponsored by University Hospital of North Norway. 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 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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