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Peripheral venous catheter complications are conditions that are frequently seen in intensive care clinics and require nursing care. The most common complications are phlebitis, infiltration and extravasation. Nurses should take the necessary precautions to prevent these complications from developing.. Therefore, this planned thesis study aims to establish an infusion monitoring system and evaluate its effectiveness in early detection of complications related to peripheral intravenous catheters. The research is planned as a randomized controlled experimental study. The study will be conducted in Ordu State Hospital General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The universe of the study will consist of patients receiving inpatient treatment in General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The sample size will be determined by g-power analysis after a two-month preliminary follow-up. Data will be collected with the "Clinical Follow-up Form", "Patient Information Form", and "Complication Follow-up Form". The clinics included in the study will be divided into two groups as experimental and control groups. First, the frequency of complications will be determined in the experimental and control groups. Then, while the control group continues its routine protocol and applications, an infusion follow-up system will be developed in the experimental group and will be used by nurses in patient care. In the final stage, the frequency of peripheral venous catheter complications will be determined again. Data will be evaluated using the SPSS 22.0 package program at a significance level of p<0.05 and a confidence interval of 95%.
Electronic monitoring systems can increase the quality of care and patient safety by enabling nurses to gain effective care and application techniques and preventing complications that may develop in patients. In addition, the integration of such technologies into clinical practices can enable nurses to act more consciously. This study can lead to the wider application of technology-based solutions in healthcare services by showing the effects of electronic monitoring systems in patient care and complication management in the scientific literature. Reductions in phlebitis, infiltration and extravasation rates improve clinical outcomes by increasing patient safety and increase the quality of life of patients. It is expected that costs will decrease with the increase in the quality of healthcare services and it is aimed to reduce the workload of nurses. Reductions in complication rates can increase the welfare of individuals by allowing patients to recover faster and shorten the duration of hospital stay. In addition, reductions in health-related complications can help reduce healthcare expenses and ease the financial burden of the state and individuals.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control Group | Active Comparator | Group where no intervention will be applied |
|
| Experimental group | Experimental | The group to which the intervention will be applied |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Infusion monitoring system developed for use by nurses in patient care | Behavioral | In the experimental group, the frequency of complications will first be determined and an infusion monitoring system will be developed and used by nurses in patient care. |
| Measure | Description | Time Frame |
|---|---|---|
| Complication Follow-up Form | This form was developed by the investigators to enable the identification and evaluation of phlebitis, infiltration and extravasation complications. This form has no minimum and maximum score. | From enrollment to the end of treatment at 10 monts |
| Measure | Description | Time Frame |
|---|---|---|
| Peripheral Edema Scale | It helps to diagnose the oedema developing in the patient. A minimum score of 1 and a maximum score of 4 is obtained from the oedema scale. The increase in the score indicates an increase in the degree of oedema and more unfavourable results. | From enrollment to the end of treatment at 10 monts |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Fatma Aksoy, MScN | Contact | +905389529328 | fatma.aksoyy96@gmail.com | |
| Şule Bıyık Bayram, PhD | Contact | sulebiyik@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Fatma Aksoy, MscN | Ordu University | Principal Investigator |
| Şule Bıyık Bayram, PhD | Karadeniz Technical University | Study Director |
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| Label | URL |
|---|---|
| Remote patient monitoring: a comprehensive study | View source |
| Design and Development of Patient Monitoring System | View source |
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I just want to share the title of the study. I want the method of the study to remain secret for now since the study is not completed.
It can start and be published 3 months after the results are published.
The data obtained from the research can be accessed after being analyzed with a suitable statistical program and the results shared.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jul 8, 2025 | Aug 8, 2025 | Prot_SAP_002.pdf |
| ICF | No | No | Yes | Informed Consent Form | Jul 8, 2025 | Aug 8, 2025 | ICF_003.pdf |
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| ID | Term |
|---|---|
| D010689 | Phlebitis |
| ID | Term |
|---|---|
| D016491 | Peripheral Vascular Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D014657 | Vasculitis |
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| ID | Term |
|---|---|
| D005791 | Patient Care |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |
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The clinics included in the study will be divided into two groups: experimental and control.
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In blinding the results, only the person performing the analysis will be blinded.
| Glasgow Coma Scale |
This scale allows the patients' level of consciousness to be assessed. Minimum 3 points and maximum 15 points can be obtained from this scale. An increase in the score indicates that the level of consciousness is better, while a decrease in the score indicates that the level of consciousness has worsened. |
| From enrollment to the end of treatment at 10 monts |