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临床试验/NCT07440849
NCT07440849招募中不适用

Combine Effects of Core Stability and Pelvic Clock Exercises on Pain, Disability and Quality of Life in Postpartum Females With Sacroiliac Joint Dysfunction

Riphah International University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1

研究概览

简要总结

The study will be a randomized control trial and will be conducted in DHQ and Sadiq Hospital in Sargodha District. This study will be completed in time duration of 10 months after the approval of synopsis. Nonprobability convenience sampling technique will be used and 50 participants will be recruited in study after randomization. The subjects will be divided into two groups. Group A(Experimental) will receive core stability and pelvic clock exercises with baseline treatment while Group B(Control) will receive only core stability exercises after baseline treatment. The tools that will be used are Numeric Pain Rating Scale (NPRS), Oswestry Disability index (ODI) and WHOQOL-BREF. Treatment have duration of 8 weeks with 3 sessions per week and an hour per session is requires. After data collection, data will be analyzed by using SPSS version 26.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Vaginal delivery
  • Primiparous women
  • Pain intensity greater than 6 on the Numerical Pain Rating Scale (NPRS)
  • Positive responses to at least three physical provocation tests suggestive of sacroiliac joint dysfunction

排除标准

  • Participants were excluded from the study if they had any of the following conditions:
  • Previous history of trauma
  • Musculoskeletal disorders (e.g., coccydynia, impingement syndrome)
  • Postpartum depression
  • Disc bulge or degeneration

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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