Evaluating pain and physical fitness in women with primary dysmenorrhea
Evaluation of Pain and Physical Fitness in Primary Dysmenorrhea
This study looks at how menstrual pain affects physical fitness, like balance and strength, in women aged 18-25 who have regular periods.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 48 (estimated) |
| Ages | 18 Years to 25 Years |
| Sex | Female |
| Sponsor | Bezmialem Vakif University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06401226 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess pain levels and various physical fitness parameters, including balance, muscle strength, and core stabilization, in women experiencing primary dysmenorrhea. Participants will be evaluated during menstruation and on a non-menstrual day to understand how menstrual pain affects physical fitness. The study focuses on women aged 18-25 with regular menstrual cycles and varying levels of pain. By comparing those with significant pain to a control group, the study seeks to highlight the impact of primary dysmenorrhea on daily activities and physical capabilities.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18-25 with a body mass index of 18-25 kg/m2 and experiencing moderate to severe menstrual pain.
Not a fit: Patients who have given birth, have chronic pain conditions, or are on hormonal treatments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the relationship between pain and physical fitness in women with primary dysmenorrhea, potentially leading to better management strategies.
How similar studies have performed: While there is limited data on similar observational studies specifically targeting primary dysmenorrhea, existing research has shown that understanding pain and physical fitness can lead to improved management of menstrual symptoms.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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
Where this trial is running
Istanbul
- Bezmialem Vakif University — Istanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Kubra Alpay — Bezmialem Vakif University
- Study coordinator: Kubra Alpay, PhD
- Email: kubraalpay@hotmail.com
- Phone: +902124012600
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.