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临床试验/NCT07308119
NCT07308119已完成不适用

Comparison Between Pilates Exercises and Aerobic Exercises in Primary Dysmenorrhea

Rana Salem Abdelghany Ali1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年12月1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
32
试验地点
1
主要终点
menstrual pain severity

研究概览

简要总结

Comparison between Pilates exercises and aerobic exercises in primary dysmenorrhea

详细描述

Primary dysmenorrhea is a common gynecological condition among young women and is characterized by painful menstrual cramps that may interfere with daily activities and quality of life. Non-pharmacological interventions, particularly therapeutic exercises, have been recommended as safe and effective approaches for managing menstrual pain. Among these interventions, Pilates exercises and aerobic exercises are widely used; however, comparative evidence regarding their relative effectiveness remains limited.

This study is designed as a comparative interventional trial to evaluate and compare the effects of Pilates exercises versus aerobic exercises on pain severity and quality of life in females with primary dysmenorrhea. Eligible participants will be allocated into two intervention groups.

Participants in Group A will undergo a structured Pilates exercise program conducted three sessions per week for eight weeks. Each session will include controlled movements focusing on core stability, flexibility, breathing control, and muscle strengthening, with a total session duration of approximately 30 minutes.

Participants in Group B will receive a supervised aerobic exercise program performed three sessions per week for eight weeks. The aerobic sessions will consist of rhythmic and continuous movements designed to improve cardiovascular endurance, with each session lasting approximately 40 minutes.

Both interventions will be delivered under standardized conditions, and participants will be instructed to maintain their usual daily activities throughout the study period. Assessments will be conducted before the start of the intervention and after completion of the eight-week exercise program to evaluate changes in menstrual pain severity and quality of life.

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

盲法说明

Participants and instructors are not blinded.

Inclusion Criteria:

  1. Females with Primary dysmenorrhea
  2. Age between 18 to 25 years
  3. Having regular menstrual cycle of 28 - 35 days
  4. Individual with BMI 18.5 to 24.9 kg/m2

Exclusion Criteria:

  1. Acute or chronic pelvic pathology
  2. Subjects having any history of regular exercises 3days/week [daily average 30-45 min]
  3. Attending physical activity like swimming, running or fitness center
  4. Who cannot perform exercise
  5. Not willing to participate

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

  • Females diagnosed with primary dysmenorrhea
  • Age between 18 and 25 years
  • Regular menstrual cycle (28-35 days)
  • Body mass index (BMI) between 18.5 and 24.9 kg/m²

排除标准

  • Presence of any acute or chronic pelvic pathology
  • History of regular exercise participation (≥3 days per week, average 30-45 minutes per day)
  • Participation in structured physical activities such as swimming, running, or fitness center training
  • Inability to perform exercise
  • Unwillingness to participate in the study

研究组 & 干预措施

Pilates exercises

Experimental

Patients will receive Pilates exercise, the exercise program was repeated 3 times 8 weeks 30 minute for each leg in session. Focused on core strengthening, flexibility, and breathing exercises to alleviate menstrual pain."

干预措施: Pilates exercises (Behavioral)

Aerobic exercises

Active Comparator

Patients will receive aerobic exercise, the exercise program was repeated 3 times 8 weeks 40minute for each session. Including walk-ing and treadmill

干预措施: Aerobic exercises (Behavioral)

结局指标

主要结局

menstrual pain severity

时间窗: 8 week

Pain intensity will be measured using the Visual Analog Scale (VAS) atbaseline and after 8 weeks of Pilates or aerobic exercises.low score zero pain and high score 10 worst pain imaginable

次要结局

  • Change quality of life(8weeks)

研究者

发起方
Rana Salem Abdelghany Ali
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Rana Salem Abdelghany Ali

Principal Investigator

Kafrelsheikh University

研究点 (1)

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