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临床试验/NCT07316036
NCT07316036进行中(未招募)不适用

The Effect of Patterned Versus Plain Fixation Materials on Pain and Physiological Parameters in Children Receiving Intravenous Therapy: A Randomized Two-Period Crossover Trial

Necmettin Erbakan University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40
试验地点
1
主要终点
Pain intensity

研究概览

简要总结

The goal of this clinical trial is to learn whether using patterned fixation materials during intravenous therapy can reduce pain and affect physiological responses in children.

Children who regularly receive intravenous therapy will take part in this study. Each participant will receive both patterned and plain fixation materials on different treatment days. Pain levels will be measured using an observation-based pain scale, and oxygen saturation and pulse rate will be recorded before and after the procedure.

详细描述

This study is a randomized two-period crossover clinical trial designed to examine whether patterned fixation materials used during intravenous (IV) catheter placement reduce pain and influence physiological responses in children. The trial focuses on children who regularly receive IV therapy for chronic conditions and aims to compare two commonly used fixation materials: patterned fixation tape and plain fixation tape.

Participants are randomly assigned to one of two sequences. In Sequence AB, children receive the patterned fixation material during their first IV procedure and the plain fixation material during their next scheduled IV procedure. In Sequence BA, children receive the plain fixation material first and the patterned fixation material during their next procedure. A washout period of at least one week naturally occurs between visits because children attend the day treatment unit weekly or every three weeks for routine therapy. This interval is considered sufficient to prevent carry-over effects, as the intervention is a short-term non-pharmacological distraction method.

During each IV procedure, pain is assessed using the FLACC behavioral pain scale by two independent observers, and physiological parameters (oxygen saturation and pulse rate) are measured one minute before and one minute after the procedure. Each child serves as their own control, allowing within-participant comparisons between the patterned and plain fixation conditions.

The primary objective of the study is to determine whether patterned fixation materials lower pain scores compared with plain fixation materials. Secondary objectives include examining whether patterned fixation materials lead to more favorable physiological responses during IV catheter insertion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
None

盲法说明

No masking was applied because the intervention involved visibly different fixation materials (patterned versus plain), making blinding of participants and healthcare providers not feasible.

入排标准

年龄范围
3 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged between 3 and 12 years
  • Children who regularly receive intravenous therapy for chronic conditions
  • Ability of the child and parent/legal guardian to understand the study procedures
  • Written informed consent obtained from the parent or legal guardian
  • Assent obtained from the child when appropriate

排除标准

  • - Presence of acute pain at the time of the procedure
  • Diagnosis of conditions that may interfere with pain assessment, such as cerebral palsy or neuromuscular or peripheral nervous system disorders
  • Requirement for more than one intravenous catheter insertion attempt during the procedure
  • Withdrawal of consent by the child or parent/legal guardian

结局指标

主要结局

Pain intensity

时间窗: Immediately after intravenous fixation during each study period

Pain intensity was assessed using the FLACC (Face, Legs, Activity, Cry, Consolability) observational pain scale. The total score ranges from 0 to 10, with higher scores indicating more severe pain.

次要结局

  • Physiological parameters, Spo2(Immediately before and immediately after each intervention period)
  • Physiological parameters, heart rate(Immediately before and immediately after each intervention period)

研究者

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

Müberra Ahsen Kalburcu

Pediatric Nurse, Graduate Researcher

Necmettin Erbakan University

研究点 (1)

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