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临床试验/NCT07002190
NCT07002190进行中(未招募)不适用

The Effect of Education Given Before Port Catheter Infusion on Infusion Related Symptoms

Karadeniz Technical University1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2024年2月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
64
试验地点
1
主要终点
Patient Identifying Information Form

研究概览

简要总结

Pain, anxiety, anxiety and changes in vital signs are observed in patients during needle insertion into the port catheter.Patients and their relatives should be informed by nurses to eliminate these problems and to provide more comfortable infusion to patients.However, studies on the care process for the symptoms that occur before port catheter infusion are limited in the literature.The thesis study planned for this purpose will be carried out to determine the effect of the training given before port catheter infusion on infusion-related symptoms.The research will be conducted as pretest-posttest, randomised controlled.Oncology-Hematology Services and Chemotherapy Unit of Karadeniz Technical University Farabi Hospital.The sample of the study will be determined by simple randomisation method and 64 patient will be included in the study.The data of the study will be collected by Patient Descriptive Information Form, Visual Analogue Scale and State and Trait Anxiety Scale, Vital Signs Follow-up Chart.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Having a port catheter
  • •The patient has no previous experience with a port catheter,
  • •The patient will receive an infusion from a port catheter for the first time,
  • •The patient's age range is between 18-70,
  • •The patient is literate,
  • •Volunteering to participate in the study,
  • •The patient will receive training from the training material for the first time.

排除标准

  • •Those with communication, hearing and vision problems,
  • •Those with any psychiatric disorder,
  • •Those who used any analgesic medication at least 8 hours before

研究组 & 干预措施

Experimental group

Experimental

The Experimental group period with the support of visual education material

干预措施: Watching an animation video (Other)

Control Group

No Intervention

The control group will take rutin patient çare.

结局指标

主要结局

Patient Identifying Information Form

时间窗: 1 day

This form, which was created by the researchers by reviewing the relevant literature, consists of 11 questions evaluating the descriptive characteristics of the patients the number of port catheter needle insertions and the information status about the port catheter.

次要结局

  • State and Trait Anxiety Scale(2 day)
  • Symptom chart(2 day)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yekta Demirsoy

nurse

Karadeniz Technical University

研究点 (1)

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