The effect of psychoeducation on pain perception and labour experience among mothers visiting labour room in IMS & SUM Hospital of Bhubaneswar, Odisha.
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
研究概览
简要总结
This randomized controlled trial aims to evaluate the effect of structured psychoeducation on pain perception and childbirth-related expectancy and experience among parturient mothers admitted to the labour room of IMS and SUM Hospital, Bhubaneswar, Odisha. A total of 84 participants will be recruited and randomly allocated into experimental (n = 42) and control (n = 42) groups. The experimental group will receive structured psychoeducation, including information on labour process, coping strategies, breathing and relaxation techniques, while the control group will receive routine standard care. Pain perception will be assessed using a standardized Pain Perception Scale at baseline before intervention and and within 24 hours after delivery, and childbirth expectancy and experience will be assessed using Wijma Delivery Expectancy/Experience Questionnaire (W-DEQ Version A and B). Data will be collected at baseline, and within 24 hours after delivery. The findings of the study are expected to provide evidence on the effectiveness of psychoeducation in improving maternal labour outcomes
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant women who are hospitalised for induction of labour or ruptured membranes without onset of contractions.
- •Women who can understand and communicate in the local language (Odia) as applicable.
- •Women who are willing to participate, provide written informed consent, and are ready to attend at least 2 sessions.
- •Women who are decide to delivery in this hospital, available for follow-up until the postpartum data collection period.
排除标准
- •Pregnant women who delivered by instrumental vaginal delivery (e.g. vacuum forcep) or caesarean section after pain scoring was performed.
- •Women with high-risk pregnancies (e.g., severe pre-eclampsia, placenta previa with bleeding, severe cardiac disease) that may affect safe participation.
研究者
Ayushi De
SUM Nursing College