CTRI/2021/09/036366已完成不适用
A comparative study on the effect of conventional TENS and acupuncture TENS on pain, physical activity and quality of life post lower segment caesarean section (LSCS). 
Sancheti Institute College of Physiotherapy1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2021年9月20日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 75
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale
研究概览
简要总结
This is a randomized, parallel group, active control trial. It is a single blinded study that studies the effect of conventional and acupuncture TENS on pain, physical activity and quality of life post LSCS. The intervention group will receive conventional TENS, acupuncture TENS and placebo TENS in 3 groups along with conventional physiotherapy treatment. The duration of TENS application will be 20 minutes for 3 days.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Outcome Assessor 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
- •Women undergone LSCS (Day 1-3) 2)Pain on VAS (having pain intensity more than 4mm) 3)Age group: 18-35 4)Subject who is conscious and oriented for device installation after anesthetic effect.
- •Subject who gives consent and is willing to participate in the clinical study.
排除标准
- •Subjects diagnosed with other diseases such as preoperative presence of maternal mental or neurological diseases affecting evaluation of pain.
- •Subjects diagnosed with psychiatric conditions.
- •Having metallic implants.
- •Altered sensations.
- •Any open wound or infection surrounding the incision site.
结局指标
主要结局
Visual Analogue Scale
时间窗: Pre and Post application of TENS
次要结局
- Kartz Index(On 1st and 3rd postoperative day, Pre and Post application of TENS)
- Brief Pain Inventory questionnaire(On 1st and 3rd postoperative day, Pre and Post application of TENS)
研究者
研究点 (1)
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