Effects of Sacral Release Technique and Lumbar Mobilization in Primary Dysmenorrhea.
2026年5月4日 更新者：Riphah International University
Comparative Effects of Sacral Release Technique and Lumbar Mobilization in Pain, Symptoms Severity and Quality of Life in Primary Dysmenorrhea.
The aim of this study is to determine the comparative effects of sacral release technique and lumbar mobilization in pain, symptoms severity and quality of life in primary dysmenorrhea.
研究概览
详细说明
This will be a randomized clinical trial, the study will be conducted at First Care Medical Complex, over 10 month duration, involving a 46 adolescent females aged 13-19 years diagnosed with primary dysmenorrhea selected through a non-probability convenience sampling technique.
Participants will be randomly assigned to two intervention groups.
Group A (n=23) will receive the Sacral Release Technique and Group B (n=23) will undergo Lumbar Mobilization.
Interventions will provide for 6 weeks, 3 sessions per cycle for two consecutive menstrual cycles.
Pain intensity will be measured by using the Numerical Pain Rating Scale (NPRS) and menstrual symptom severity will be evaluated using a structured symptom rating tool, and quality of life will be measured using EuroQOL.
Data will be analyzed using SPSS version 25, and with p-value of <0.05 will be considered statistically significant.
研究类型
介入性
注册 (估计的)
46
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：imran G amjad
- 电话号码：03324390125
- 邮箱：imran.amjad@riphah.edu.pk
学习地点
-
-
Punjab Province
-
Lahore、Punjab Province、巴基斯坦、6400
- 招聘中
- Ittefaq Hospital
-
接触：
- hina G gul, PhD*
- 电话号码：03214979172
- 邮箱：hina.gul@riphah.edu.pk
-
首席研究员：
- Tanzila Nasrullah, MSPT(WH)
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
接受健康志愿者
是的
描述
Inclusion Criteria:
- Unmarried female
- Diagnosed with primary dysmenorrhea through WaLIDD Score
- Regular menstrual cycles (21-35 days)
- Pain score of > 4 on the Numerical Pain Rating Scale (NPRS) during menstruation
Exclusion Criteria:
- Any pelvic inflammatory disease
- Obesity
- PCOS
- Spinal deformity
- Lumber radiculopathy
- Heavy menstrual bleeding (menorrhagia)
- Irregular menstrual cycles
- Spine trauma and coccyx pain
- History of pelvic or spinal surgery currently on hormonal therapy or other ongoing physiotherapy for dysmenorrhea
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：SACRAL RELEASE TECHNIQUE
The sacral release technique is a gentle, non-invasive method used to relieve tension in the sacral area, improve pelvic alignment, and enhance overall comfort, particularly during pregnancy
|
The therapist will maintain gentle, sustained holds for 3 to 5 minutes per repetition, with 2 to 3 repetitions per session.
Each session lasted 15 to 20 minutes.
3 times per week over a period of two consecutive menstrual cycles, for six-weeks period
|
|
有源比较器：LUMBAR MOBILIZATION
Lumbar mobilization is a manual therapy technique used to relieve pain, restore joint motion, and improve mobility in the lower spine.
|
Treatments will be administered three times per menstrual cycle over a six-weeks period
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Numerical Pain Rating Scale (NPRS)
大体时间：6th week
|
The Numerical Pain Rating Scale (NPRS) is a unidimensional scale ranging from 0 (no pain) to 10 (worst possible pain).
The NPRS demonstrates excellent test-retest reliability, with Intraclass Correlation Coefficients (ICC) typically above 0.90, indicating stability of responses over time.
Its internal consistency has been shown to be high, with Cronbach's alpha values ranging from 0.86 to 0.95, reflecting a strong degree of reliability.
The tool also has validity as it correlates significantly with other pain-related outcome measures domains of quality-of-life instruments
|
6th week
|
|
Menstrual Symptom Questionnaire (MSQ)
大体时间：6th week
|
It is a validated instrument designed to assess the frequency and intensity of common menstrual-related symptoms, including pain, mood changes, fatigue, bloating, and general discomfort.
It provides a comprehensive overview of both physical and emotional aspects of menstruation, making it suitable for evaluating the effectiveness of interventions in conditions like primary dysmenorrhea.
The scale demonstrates acceptable internal consistency, with a reported Cronbach's alpha of 0.78, indicating reliable measurement across diverse symptom domain
|
6th week
|
|
EuroQol-5 Dimension Questionnaire (EQ-5D)
大体时间：6th week
|
The EuroQol-5 Dimension Questionnaire (EQ-5D) is assessing health-related quality of life in women with primary dysmenorrhea.
The internal consistency of the EQ-5D in related populations have reported a Cronbach's alpha ranging from 0.70 to 0.89, indicating acceptable to excellent reliability
|
6th week
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：sobia ghafoor, t-DPT、Riphah International University
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Gottschewsky, N., D. Kraft, and T.J.B.o.s.D. Kaufmann, Menarche, pubertal timing and the brain: female-specific patterns of brain maturation beyond age-related development. 2024. 15(1): p. 25.
- Wu, X., et al., Age at Menarche, Menopause Status and Metabolic Syndrome and its Components: Findings from the Henan Rural Cohort Study. 2023. 131(09): p. 463-471.
- Qureshi, M.A., et al., Coping Mechanisms of Menopausal Women and Its Impact on the Quality of Life at Mohan Pura, Rawalpindi. 2025. 15(3): p. 197-202
- Rana, M.Y., et al., Factors influencing the age of menopause among Pakistani women. 2021. 11(3): p. 214-216.
- Keshwani, N., et al., Update in Adolescent Medicine, in Update in Pediatrics. 2024, Springer. p. 3-57.
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2025年10月1日
初级完成 (估计的)
2026年6月1日
研究完成 (估计的)
2026年7月1日
研究注册日期
首次提交
2026年5月4日
首先提交符合 QC 标准的
2026年5月4日
首次发布 (实际的)
2026年5月8日
研究记录更新
最后更新发布 (实际的)
2026年5月8日
上次提交的符合 QC 标准的更新
2026年5月4日
最后验证
2026年5月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.