跳至主要内容
临床试验/NCT07155876
NCT07155876Enrolling By Invitation不适用

Exploring the Effect of Aromatherapy Inhalation for Managing Pain, Anxiety, and Nausea/Vomiting Throughout the Laboring Process

Baptist Health South Florida2 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2025年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
128
试验地点
2
主要终点
Relief of nausea/vomiting

研究概览

简要总结

To explore the effect of aromatherapy in laboring patients with pain, anxiety, and/or nausea/vomiting.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Pregnant patients at least 18 years old in spontaneous labor or induction of labor (despite transitioning into a caesarean section)

排除标准

  • •Patients who are unable to detect scents/odors
  • •Patients with known allergies to aromatherapy and/or its components

研究组 & 干预措施

Intervention group: Education video

Experimental

The participant receives aromatherapy plus standard of care (SoC) for treatment based on symptoms (anxiety, pain, and/or nausea/vomiting) as prescribed by the physician.

干预措施: Aromatherapy plus standard of care (Other)

Control group: Standard of Care

Other

The patient receives SoC for treatment of based on symptoms (anxiety, pain, and/or nausea/vomiting) as prescribed by the physician.

干预措施: Standard of Care Only (Other)

结局指标

主要结局

Relief of nausea/vomiting

时间窗: Measured before and after receiving standard of care (SoC) or Intervention+SoC.

Measured in the control and intervention groups before and after receiving treatment (yes or no - presence of nausea/vomiting).

Decreased anxiety

时间窗: Measured before and after receiving standard of care (SoC) or Intervention+SoC.

Measured before and after receiving treatment in both the control and intervention groups. Anxiety level = 0 =none, 1 = minimal (a little), 2 = moderate (medium), and 3 = severe (a lot).

Pain relief (scale of 0 to 10)

时间窗: Measured before and after receiving standard of care (SoC) or Intervention+SoC.

Level of pain is measured before and after receiving treatment in both the control and interventions groups. Pain is measured on a scale of 0 to 10 (0 = no pain, 10 = severe pain).

次要结局

未报告次要终点

研究者

发起方
Baptist Health South Florida
申办方类型
Other
责任方
Sponsor

研究点 (2)

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