跳至主要内容
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)

Loading locations...

相似试验

The Role of Therapeutic Ultrasound in Comparison... | 临床试验