跳至主要内容
临床试验/NCT07549789
NCT07549789尚未招募不适用

Effect of Foot Reflexology on Comfort and Physiological Parameters in Neonates With Hypoxic-Ischemic Encephalopathy Undergoing Therapeutic Hypothermia: A Randomized Controlled Trial

Istanbul Nisantasi University1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2026年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
84
试验地点
1
主要终点
ComfortNeo score

研究概览

简要总结

This randomized controlled trial aims to evaluate the effect of foot reflexology on comfort levels and physiological parameters in neonates with hypoxic-ischemic encephalopathy undergoing therapeutic hypothermia. Neonates in the intervention group will receive standardized foot reflexology sessions in addition to routine care, while the control group will receive routine care alone. Comfort will be assessed using the COMFORTneo scale, and physiological parameters will be monitored throughout the intervention period.

详细描述

Hypoxic-ischemic encephalopathy (HIE) is a major cause of neonatal morbidity and mortality, and therapeutic hypothermia (TH) is the standard treatment to reduce neurological injury. However, during TH, the management of pain, distress, and comfort remains challenging, and evidence regarding optimal supportive care strategies is limited. Pharmacological approaches may have potential adverse effects, highlighting the need for safe and effective non-pharmacological interventions.

Foot reflexology is a complementary therapy based on the stimulation of specific points on the feet, which is thought to promote autonomic regulation, improve circulation, and enhance relaxation. In neonatal populations, existing studies on reflexology and similar tactile interventions have primarily focused on procedural pain and short-term outcomes. Evidence regarding sustained comfort and physiological regulation, particularly in critically ill neonates undergoing therapeutic hypothermia, remains scarce.

This study is designed as a randomized controlled trial to evaluate the effect of foot reflexology on comfort and physiological parameters in neonates with HIE undergoing TH. Participants will be randomly assigned to either an intervention group receiving foot reflexology in addition to routine care or a control group receiving routine care alone.

The reflexology intervention will be applied in a standardized manner during the hypothermia period by a trained practitioner. The protocol is structured to ensure consistency, safety, and compatibility with intensive care conditions.

Comfort will be assessed using the COMFORTneo scale, a validated and reliable tool for evaluating prolonged pain and distress in neonates. In addition, physiological parameters including heart rate, respiratory rate, oxygen saturation, mean arterial pressure, and body temperature will be monitored to assess physiological stability.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
30 Minutes 至 3 Hours(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with hypoxic-ischemic encephalopathy
  • Undergoing therapeutic hypothermia
  • Hemodynamically stable neonates

排除标准

  • Major congenital anomalies
  • Hemodynamic instability
  • Skin integrity problems preventing foot reflexology

研究组 & 干预措施

Foot Reflexology

Experimental

Foot reflexology will be applied in addition to standard care during therapeutic hypothermia. Each session will last approximately 7 minutes (3.5 minutes per foot) and will be performed once daily for three consecutive days by a trained healthcare professional using standardized techniques.

干预措施: Foot reflexology (Other)

Standard Care

Active Comparator

Participants will receive standard therapeutic hypothermia and routine neonatal intensive care without any additional tactile stimulation or reflexology.

干预措施: Standard care (Other)

结局指标

主要结局

ComfortNeo score

时间窗: From baseline up to 72 hours after intervention

The COMFORTneo scale is a clinically validated tool specifically designed to assess prolonged pain and distress in preterm and term neonates within the NICU. It is a modification of the original COMFORT scale, optimized for newborn physiology. The scale evaluates six behavioral parameters, each scored from 1 to 5: Alertness: State of sleep or wakefulness. Calmness/Agitation: Level of anxiety or peacefulness. Respiratory Response/Crying: Quality of breathing or crying intensity. Physical Movement: Frequency and vigor of body activity. Muscle Tone: Level of bodily tension or relaxation. Facial Tension: Presence of grimacing or tension. Total scores range from 6 to 30. A cutoff score of 14 or higher typically indicates significant distress, requiring clinical intervention. It is ideal for monitoring sedation and comfort in neonates undergoing Therapeutic Hypothermia.

Outcome

时间窗: Immediately before and within 10 minutes after each session for 3 consecutive days

Heart Rate

次要结局

未报告次要终点

研究者

发起方
Istanbul Nisantasi University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alev Sivasli

Assistant Professor

Istanbul Nisantasi University

研究点 (1)

Loading locations...

相似试验