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Association Between Menstrual Pain Severity and Plantar Pressure in Young Women

2026年11月9日 更新者:Al Hayah University In Cairo

Association Between Primary Dysmenorrhea Severity and Plantar Pressure Distribution in Post-Pubertal Females

Primary dysmenorrhea is a common condition characterized by recurrent menstrual pain in the absence of identifiable pelvic pathology. Menstrual pain may be accompanied by changes in posture, neuromuscular function, and postural control. These changes may influence how body weight is distributed across the feet during standing.

The purpose of this observational study is to investigate the association between primary dysmenorrhea severity and plantar pressure distribution in post-pubertal females.

The study will include 79 female university students aged 18-23 years with a history of primary dysmenorrhea. Participants will be recruited from the first through fourth academic years of the Faculty of Physical Therapy at Al Hayat University in Cairo, Egypt.

Each participant will undergo a single assessment during the menstrual phase, specifically within the first three days of menstruation.

Primary dysmenorrhea severity will be assessed using the Working Ability, Location, Intensity, Days of Pain, Dysmenorrhea (WaLIDD) scale. The scale produces a total score ranging from 0 to 12, with higher scores indicating greater severity.

Plantar pressure distribution will be assessed using the DIERS pedoscan system during standardized barefoot quiet standing. The assessment will include plantar pressure distribution and anterior-posterior and right-left weight distribution.

A minimum of two valid 30-second standing measurements will be obtained and averaged for analysis.

The study will examine whether greater primary dysmenorrhea severity is associated with measurable differences in plantar pressure distribution and weight-bearing characteristics.

No therapeutic intervention, randomization, or experimental treatment allocation will be performed.

研究概览

地位

招聘中

研究类型

观察性的

注册 (估计的)

79

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

学习地点

      • New Cairo、埃及
        • 招聘中
        • Alhayah University in Cairo

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

18年 至 23年 (成人)

接受健康志愿者

不

有资格学习的性别

女性

取样方法

非概率样本

研究人群

The study population consists of female undergraduate physical therapy students aged 18-23 years attending the first through fourth academic years at Al Hayat University in Cairo, Egypt. Eligible participants will have primary dysmenorrhea, regular menstrual cycles, and the ability to complete a standardized standing plantar pressure assessment. A total of 79 participants is planned. Each participant will be assessed during menstrual Days 1-3.

描述

Inclusion Criteria:

  • Post-pubertal females aged 18-23 years.
  • Regular menstrual cycles ranging from 21 to 35 days.
  • History consistent with primary dysmenorrhea for at least the previous six consecutive months.
  • Ability to stand independently without assistive devices for the duration of the pedobarographic assessment.
  • Provision of written informed consent before participation.

Exclusion Criteria:

  • Diagnosis of secondary dysmenorrhea, including endometriosis, adenomyosis, pelvic inflammatory disease, or uterine fibroids, confirmed clinically or through imaging.
  • Current or recent pregnancy.
  • Neurological disorders affecting balance or sensorimotor function.
  • Musculoskeletal injury or condition involving the lower limbs, feet, or lumbar spine within the preceding six months.
  • Foot deformity or structural lower-limb abnormality known to alter plantar pressure distribution.
  • Current use of medications known to influence postural control, including centrally acting analgesics, benzodiazepines, or antiepileptics.
  • History of major lower-limb or foot surgery.
  • Systemic disease affecting sensory or motor function, including diabetes mellitus or peripheral neuropathy.

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

  • 观测模型:CASE_ONLY
  • 时间观点:CROSS_SECTIONAL

队列和干预

团体/队列
干预/治疗
Post-Pubertal Females With Primary Dysmenorrhea

A single group of 79 post-pubertal females aged 18-23 years with primary dysmenorrhea will be recruited from undergraduate physical therapy students at Al Hayat University in Cairo. Participants will have regular menstrual cycles, a history of primary dysmenorrhea for at least six consecutive months, and the ability to stand independently for pedobarographic assessment. Dysmenorrhea severity and plantar pressure parameters will be assessed at a single visit during menstrual Days 1-3.

The exposure of interest is the severity of primary dysmenorrhea, quantified using the self-reported WaLIDD scale. The instrument evaluates working ability, pain location, pain intensity, and duration of pain. Each domain contributes 0-3 points to a total score ranging from 0 to 12. Higher scores indicate greater severity. Dysmenorrhea severity will be examined for its association with objectively measured plantar pressure distribution and weight-bearing characteristics during standing. This is an observed characteristic and not an investigator-assigned intervention.

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
Static Plantar Pressure Distribution
大体时间:Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.

Plantar pressure distribution will be assessed using the DIERS pedoscan computerized pedobarographic platform during standardized barefoot quiet standing. Participants will stand with feet shoulder-width apart, arms relaxed at their sides, and eyes directed forward. At least two valid 30-second recordings will be obtained and averaged. The recorded plantar loading distribution will be analyzed in relation to primary dysmenorrhea severity. The precise regional pressure outputs and measurement units must be defined from the study's DIERS reporting protocol before submission.

Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.
Primary Dysmenorrhea Severity Assessed by WaLIDD Score
大体时间:Single assessment during menstrual Days 1-3.

Primary dysmenorrhea severity will be quantified using the Working Ability, Location, Intensity, Days of Pain, Dysmenorrhea (WaLIDD) scale. The instrument contains four domains, each scored from 0 to 3, resulting in a total score ranging from 0 to 12. Higher scores represent greater symptom severity. Scores are categorized as absent (0), mild (1-4), moderate (5-7), or severe (8-12). The total score will be used as the principal severity variable in the correlational analysis.

Single assessment during menstrual Days 1-3.

次要结果测量

结果测量
措施说明
大体时间
Anterior-Posterior Weight Distribution (%)
大体时间:Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.

Anterior-posterior weight distribution will be measured using the DIERS pedoscan system during standardized barefoot quiet standing. The instrument will quantify the distribution of body weight between the anterior and posterior plantar regions, expressed as percentages. At least two valid 30-second recordings will be obtained and averaged for analysis.

Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.
Right-Left Weight Distribution (%)
大体时间:Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.

Right-left weight distribution will be assessed using the DIERS pedoscan computerized pressure platform. The measurement will quantify the percentage of body weight distributed between the right and left lower limbs during standardized barefoot quiet standing. At least two valid 30-second recordings will be obtained and averaged for analysis.

Single assessment during menstrual Days 1-3; at least two 30-second standing recordings.

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。

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 (估计的)

2026年11月18日

初级完成 (估计的)

2027年2月1日

研究完成 (估计的)

2027年2月1日

研究注册日期

首次提交

2026年11月9日

首先提交符合 QC 标准的

2026年11月9日

首次发布 (实际的)

2026年11月13日

研究记录更新

最后更新发布 (实际的)

2026年11月13日

上次提交的符合 QC 标准的更新

2026年11月9日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • AOMS-PD-PPD-2026-001 Copy

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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