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临床试验/NCT06401226
NCT06401226招募中不适用

Evaluation of Pain and Physical Fitness in Primary Dysmenorrhea

Bezmialem Vakif University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2023年6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
48
试验地点
1
主要终点
Core stability

研究概览

简要总结

The aim of this study is to evaluate pain and physical fitness parameters such as balance, muscle strength, and core stabilization in primary dysmenorrhea.

详细描述

Primary dysmenorrhea (PD) is a condition that occurs just before or during menstruation and is accompanied by cramp-like pain in the lower abdomen, without any pelvic pathology. Pain usually begins just before or during menstruation and ends within 12-72 hours. Most women with PD describe their menstrual pain as moderate to severe, which significantly affects their activities of daily living and school and work performance.

In PD, functions and activities of daily living are also affected due to pain and other hormonal changes. Studies have reported that musculoskeletal problems such as decreased spinal mobility, pelvic stability and postural control are observed in women with dysmenorrhea.

The aim of this study is to evaluate pain and physical fitness parameters such as balance, muscle strength, and core stabilization during the menstruation and on a non-menstrual day of the cycle, in primary dysmenorrhea.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

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

入选标准

  • Between the ages of 18-25
  • Body mass index of 18-25 kg/m2
  • Having a regular menstrual cycle (28±7 days)
  • For the PD Group; pain level >5 according to VAS during menstruation
  • For the Control Group; having a VAS score of 5 or less

排除标准

  • Having given birth before
  • Using an intrauterine device
  • Having a health problem that causes chronic pain
  • Having a diagnosis of neurological, orthopedic, vestibular, rheumatological disorder
  • Being diagnosed with a gynecological or pelvic disorder such as endometriosis, ovarian cyst
  • Having a history of abdominal or gynecological surgery within the last year
  • Being on oral contraceptive use/hormonal therapy or antidepressant treatment
  • Having used painkillers 12 hours before the evaluation
  • Participating in a regular exercise program

结局指标

主要结局

Core stability

时间窗: 2 weeks

A pressurized biofeedback device will be used to evaluate core stability. The device will initially be set to 70 mmHg pressure and changes in pressure will be recorded for analysis at the end of the evaluation.

Pain assessment

时间窗: 2 weeks

Pain assessment will be evaluated with a visual analog scale. Subjects will be asked to mark the intensity of the pain they feel on a 10 cm line, where "0" means no pain and "10" means very severe pain.

Balance

时间窗: 2 weeks

Biodex Balance System (Biodex Medical Systems, Inc. USA) will be used in the dynamic postural stability test and sensory integration of balance clinical test evaluations.

Lower extremity muscle strength

时间窗: 2 weeks

A 30-second sit to stand test will be used to evaluate the individual's lower extremity muscle strength and functional capacity. The number of repetitions performed in 30 seconds is recorded.

次要结局

  • Menstrual symptoms(2 weeks)
  • Lower extremity flexibility(2 weeks)
  • Depression, anxiety and stress symptoms(2 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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