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临床试验/CTRI/2025/08/092204
CTRI/2025/08/092204尚未招募2 期

Effectiveness of Early Ambulation in Reducing Postoperative Complications Among Post-Cesarean Section Mothers: A Randomized Controlled Trial

The study is not sponsored by any agency or research instituttion1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2025年8月20日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
52
试验地点
1
主要终点
Pain,headache,Involution of uterus

研究概览

简要总结

This randomized controlled trial aims to assess the effectiveness of early ambulation in reducing postoperative complications among post cesarean section mothers. Participants who meet the inclusion criteria will be randomly allocated to two groups using day wise block randomization. The intervention group will receive structured early ambulation beginning 8 to 10 hours after surgery, while the control group will receive routine postoperative care. The early ambulation protocol includes deep breathing exercises, limb movements, position changes in bed, assisted sitting and walking, and daily step count monitoring using a pedometer. Outcomes such as pain, uterine involution, wound healing, headache, psychological wellbeing, and physical activity will be assessed using validated tools like the Numerical Pain Rating Scale, Obstetric Quality of Recovery Score Hindi version, Edinburg Postnatal Depression Scale Hindi, GAD 7 Hindi, Southampton Wound Assessment Scale, and Homan’s sign. The study will be conducted at a tertiary care institute in India and will follow ethical guidelines. The findings are expected to provide evidence for integrating early ambulation into routine post cesarean care to improve recovery and reduce complications.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
Female

入选标准

  • Those who are willing to participate Those who received spinal anaesthesia Those who undergone LSCS Those who are hemodynamically stable after LSCS.

排除标准

  • Mother with PPH
  • Those who undergone classical C section
  • Diagnosed with psychiatric illness
  • Those who received general anaesthesia
  • Those who already had DVT
  • Those who have increased intracranial pressure
  • Mother with baby in NICU.

结局指标

主要结局

Pain,headache,Involution of uterus

时间窗: Day Zero,Day One,Day Three

次要结局

  • Psychological Wellbeing,Recovery,Health(Day 1 and Day 3)

研究者

发起方
The study is not sponsored by any agency or research instituttion
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

DrAbin Varghese

AIIMS,Nagpur

研究点 (1)

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