Neuroma-Associated Pain Management After Combat-Related Trauma in Ukraine
This study is recruiting. It focuses on depression and currently lists participation information in Ukraine.
Key information made simple
This study is looking at whether a digital support tool can help people with depression. Participants receive a study treatment and complete follow-up visits and assessments. Taking part may give some people access to a digital support tool, but direct benefit is not guaranteed.
Your next step
The official record suggests in-person participation through a hospital, with sites including Communal enterprise "Yuri Semenyuk Rivne Regional Clinical Hospital" of Rivne Regional Council. 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 being able to follow the planned visits or tasks, while common reasons not to take part include pregnancy or breastfeeding 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
- Time commitment
- long follow-up or multiple visits
- Study phase
- Not available
- Enrollment
- Not available
- Recruitment status
- Recruiting
- Sponsor
- Ukrainian Society of Regional Anesthesia and Pain Therapy
- Sponsor type
- Unknown or unclear
- Main activity
- digital app or tool
- Intervention
- Not available
- Source
- Official registry link
Want help reviewing this study?
Key study information
- Condition
- Depression, Pain Management, ...
- Study status
- Recruiting
- Sponsor / lead affiliation
- Ukrainian Society of Regional Anesthesia and Pain Therapy
- Location / country
- Ukraine
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT07416448
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 Ukraine.
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.
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT07416448
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 Neuroma-Associated Pain Management After Combat-Related Trauma in Ukraine?
This study is exploring digital app or tool 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 Ukrainian Society of Regional Anesthesia and Pain Therapy. We could not clearly classify the sponsor type from the available data. Check the official source record to verify who is responsible for the study.
What does participation involve, what phase is it, and what should I ask about safety?
This study may involve digital app or tool, 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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