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临床试验/NCT07246369
NCT07246369已完成不适用

The Role of Therapeutic Ultrasound in Comparison With Electrical Dry Needling in Chronic Low Back Patients Post Cesarean Section

University of Lahore1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年10月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36
试验地点
1
主要终点
Numeric Pain Rating Scale (NPRS)

研究概览

简要总结

HYPOTHESIS

Null Hypothesis (HO):

There was a non-significant difference in the role of therapeutic ultrasound in comparison with electrical dry needling in chronic low back patients post cesarean-section.

Alternative Hypothesis (HA):

There was a significant difference in the role of therapeutic ultrasound in comparison with electrical dry needling in chronic low back patients post cesarean-section.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
25 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Female patients aged 25-35 years.
  • •History of cesarean section with epidural anesthesia
  • •Within the past 6 months to 8 months.
  • •Primiparous, postpartum women.
  • •Chronic low back pain persisting for more than 3 months.
  • •Pain intensity of at least four on a Numeric Pain Rating Scale (NPRS).

排除标准

  • •Previous low back surgery.
  • •Multiparous, postpartum women.
  • •History of Fracture (pubic fractures, vertebral fracture) and osteoporosis
  • •Having a stillborn fetus or lethal induction of labor.
  • •Severe comorbid conditions (e.g., uncontrolled diabetes, cardiovascular disease).
  • •Patients who experienced a C-section with general anesthesia

研究组 & 干预措施

Group B (Therapeutic Ultrasound)

Active Comparator

干预措施: Ultrasound (Other)

Group A (Electrical Dry Needling)

Experimental

干预措施: Electrical Dry Needling (Other)

结局指标

主要结局

Numeric Pain Rating Scale (NPRS)

时间窗: Baseline to 6 Week

Participants in the study expressed the severity of their pain using a 10 Numeric Pain Rating Scale (NPRS). Participants are instructed to locate their level of pain on a 10-mm horizontal line, with 0 mm representing "no pain" and 10 mm representing "the most severe pain."

Tampa Scale for Kinesiophobia (TSK)

时间窗: Baseline to 6 Week

It is a measurement tool used to assess individuals' fear of movement and re-injury. This 17-item questionnaire is designed to determine an individual's fear of movement and the possibility of (re)injury. Patients evaluate their beliefs on their kinesiophobia using a 4-point scale that spans from strongly disagree to strongly agree.

次要结局

未报告次要终点

研究者

发起方
University of Lahore
申办方类型
Other
责任方
Sponsor

研究点 (1)

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