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临床试验/CTRI/2025/10/095703
CTRI/2025/10/095703尚未招募不适用

Effectiveness of Proprioceptive Neuromuscular Facilitation(PNF) programme on abdominal pain,strength,balance and Functional activity in postpartum women.

Supreet Kaur1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2025年11月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
54
试验地点
1
主要终点
Improvement in abdominal pain,weakness,balance and functional activity at the end of PNF pragramme

研究概览

简要总结

This is a randomized ,parallel- group controlled trial comparing 54 postpartum women,randomized into two groups :one receiving PNF Programme,the other receiving standard care and advice only over the period of 3 days .Abdominal pain,weakness,balance and functional activity will be measured before and after the completion of programme in both the groups.Participation will be voluntary and written informed consent will be obtained from all the participants.This study will test efficacy of PNF in postpartum recovery over routine standaized care and advice and will provide useful insights to guide future postpartum rehabilitation strategies.

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
20.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • 1.Postpartum women having abdominal pain.
  • 2.Postpartum women having weak abdominals.
  • 3.Postpartum women having balance impairement.
  • 4.Postpartum women having functional activity impairment.
  • 5.Postpartum women between 20 to 35 years of age 6.Primiparous Postpartum women.

排除标准

  • 1.Postpartum women having abdominal pain,abdominal weaknes,balance impairement,functional impsirement due to reasons other than pregnsncy.
  • 2.Postpartum women under anaesthesia.
  • 3.Postpartum women having any fractures.
  • 4.Postpartum women having seizures.

结局指标

主要结局

Improvement in abdominal pain,weakness,balance and functional activity at the end of PNF pragramme

时间窗: Relevant Data will be collected just before the 1st session(1day),after 3rd session(2nd day) and after 6th session(3rd day) of entire PNF Program.

次要结局

  • patient satisfaction levels with interventions(data for patient satisfaction levels will be collected on 3rd day i.e. at termination of entire PNF Programme.)

研究者

发起方
Supreet Kaur
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Supreet Kaur

Guru Nanak Dev University ,Amritsar

研究点 (1)

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