Professional Contributions and Social Value in High-Acuity Medical Care Settings (NCT07686666) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Professional Contributions and Social Value in High-Acuity Medical Care Settings
1,350 participantsStarted 2026-06-25
Plain-language summary
This study will explore experiences in high-acuity medical care settings, such as emergency, trauma, intensive care, and related clinical areas. These settings often involve heavy workloads, complex care decisions, teamwork, and communication among many people.
The study will invite healthcare professionals, patients, important family caregivers, and other related people to share their experiences. Participants may complete questionnaires, take part in interviews, or complete a later online survey. The study will ask about work experiences, care experiences, communication, support needs, teamwork, and the value of professional contributions in these settings.
The goal of this study is to better understand important but less visible contributions in high-acuity medical care, such as teaching, coordination, communication, and support. The findings may help identify areas that can be considered in future research, hospital improvement, workforce development, and policy discussion.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adults aged 18 years or older who are able to understand the study information and provide informed consent or agreement to participate.
* Healthcare professionals working in hospital-based high-acuity clinical areas, such as emergency departments, trauma and critical care, intensive care units, respiratory care units, and related settings. Eligible participants may include physicians, nurses, allied health professionals, case managers, registry or data management personnel, and administrative staff involved in these areas.
* Patients who have received care in high-acuity medical care settings.
* Important family members or main caregivers who have accompanied, cared for, or supported decision-making for patients in high-acuity medical care settings.
* Public-sector or emergency response personnel involved in emergency care, rescue, health, or social service systems related to high-acuity medical care.
For the first phase, healthcare professionals may be invited to complete questionnaires and/or participate in qualitative interviews. Patients, important family caregivers, and other relevant stakeholders may be invited to participate in qualitative interviews. For the second phase, eligible stakeholder groups may be invited to complete an anonymous online survey.
Exclusion Criteria:
* Individuals who decline to participate after receiving the study explanation.
* Individuals who do not meet the inclusion criteria.
* Individuals who are unable to under…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Number of preliminary social value domains with potential relevance for future indicator development identified in high-acuity medical care settings
Timeframe: Through completion of qualitative interview, questionnaire, and survey data collection, up to 54 months
Trial details
NCT IDNCT07686666
SponsorKaohsiung Medical University Chung-Ho Memorial Hospital