Study on the Influence of Humanized Nursing Model on the Effect of Intravenous Infusion Care (NCT06569914) | Clinical Trial Compass
CompletedNot Applicable
Study on the Influence of Humanized Nursing Model on the Effect of Intravenous Infusion Care
China40 participantsStarted 2024-09-01
Plain-language summary
The routine nursing content is relatively simple, and nursing measures are greatly influenced by the personal experience of nursing staff, lacking a systematic approach Sexuality, scientificity, and relatively late implementation have resulted in unsatisfactory preventive effects. Early nursing intervention emphasizes the importance of patients The impact of early postoperative intervention can effectively meet the cognitive needs of patients and improve their compliance with treatment and care At the same time, early intervention can help patients avoid risks and better achieve nursing goals. This selection A study was conducted on 40 patients receiving intravenous infusion to explore the impact of humanized nursing on the effectiveness of intravenous infusion nursing.
Who can participate
Age range
18 Years – 100 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:
* Patients receiving intravenous infusion in our hospital
* Have complete clinical data
* Know and sign the informed consent form
Exclusion Criteria:
* Underage patients
* Patients with consciousness and cognitive impairments
* Patients with mental illness
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
Hamilton Depression Scale
Timeframe: Up to 24 hours (during intravenous infusion)
2
Self-made scale
Timeframe: Up to 24 hours (during intravenous infusion)
Trial details
NCT IDNCT06569914
SponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine