Relationship Between Primary Dysmenorrhea and Biomechanical Characteristics of Lumbo-pelvic Region Among Female University Students
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Females with primary dysmenorrhea, Females without dysmenorrhea.
- Who it may be relevant to
- Registry conditions: Dysmenorrhea Primary. Basic parameters: 18 years — 24 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
this study will be conducted to Investigate the relationship between primary dysmenorrhea and biomechanical characteristics of lumbo-pelvic region among female university students
Detailed description
Dysmenorrhea is a highly prevalent menstrual health problem among female university students and represents a significant under recognized women's health issue. Cultural perceptions that normalize menstrual pain often result in underreporting, delayed healthcare seeking, and inadequate management among young women. This study is significant in addressing dysmenorrhea as a health condition that affects the physical, psychological, academic, and social well-being of female university students. From a physical health perspective, dysmenorrhea can lead to reduced mobility, fatigue, sleep disturbances, and musculoskeletal pain, particularly in the lumbopelvic region. Psychologically, recurrent menstrual pain may contribute to increased stress, anxiety, emotional distress, and reduced concentration. In the demanding academic environment of universities, these factors can negatively influence academic performance and mental well-being. Socially and academically, dysmenorrhea is a leading cause of class absenteeism, decreased lecture attendance, and reduced participation in practical and clinical sessions among female students.
Interventions
- Other Females with primary dysmenorrhea
Female university students aged 18-24 years, Body Mass Index (BMI) between 18.5 and 24.9 kg/m² with primary dysmenorrhea (NRS \> 4). - Other Females without dysmenorrhea
Female university students aged 18-24 years, with a Body Mass Index (BMI) between 18.5 and 24.9 kg/m² without dysmenorrhea (NRS less 3).
Primary outcome measures
- life disability [Time frame: up to one day]
Secondary outcome measures (8)
- pain intensity [Time frame: up to one day]
- pelvic tilt angle [Time frame: up to one day]
- muscle activity [Time frame: up to one day]
- oscillatory frequency [Time frame: up to one day]
- muscle dynamic stiffness [Time frame: up to one day]
- muscle elasticity [Time frame: up to one day]
- mechanical stree relaxation time [Time frame: up to one day]
- muscle viscoelastic property [Time frame: up to one day]
Eligibility criteria
Inclusion criteria
- Female university students aged 18-24 years
- Body Mass Index (BMI) between 18.5 and 24.9 kg/m²
- Regular menstrual cycle (28-35 days) for at least the past six months
- Willingness to avoid analgesics 72 hours prior to testing
Exclusion criteria
- History of pelvic or gynecological disorders
- Previous spinal, abdominal, or lower limb surgery
- Neurological disorders
- Structural spinal deformities (e.g., moderate to severe scoliosis)
- Obesity (BMI ≥ 30 kg/m²)
- Current use of oral contraceptive pills
- History of pregnancy or delivery
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07702214 · P.T.REC/012/006448