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