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Pelvic Floor Muscle Activity in Primary Dysmenorrhea

Pelvic Floor Muscle Activity in Primary Dysmenorrhea

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06803173
Enrollment
77
Registered
2025-01-31
Start date
2025-02-01
Completion date
2025-04-15
Last updated
2025-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Dysmenorrhea

Brief summary

This study will be conducted to assess the pelvic floor muscle (PFM) activity in primary dysmenorrhea (PD).

Detailed description

Dysmenorrhea, marked by painful menstrual cramps, often involves increased PFM tension, spasms, and inflammation, affecting females' quality of life and productivity. The traditional focus has been on investigating the abdominal region in women with PD. However, this new perspective considers that the hormonal changes experienced during the menstrual cycle in PD patients may lead to a heightened sensitivity of the PFM, not just the abdominal area. This suggests that the pain associated with PD may have a more widespread impact on the pelvic region rather than being localized to the abdomen. Pelvic floor myofascial trigger points (MTrPs) may also exacerbate menstrual pain through the neural pathway. There is a critical gap in the literature regarding the nature of the association between dysmenorrhea and PFM activity in this population. Yet, it is unknown whether the pain is a cause or result of increased PFM tone, and the nature of the association between menstrual pain and PFM tone in women with PD is also unknown. So, this study utilizes transabdominal ultrasound (TAU) to examine PFM activity in PD, aiming to clarify how PFM activity contributes to menstrual pain. Understanding these dynamics could lead to preventive strategies and educational efforts highlighting the role of pelvic floor interventions in managing dysmenorrhea, potentially improving treatment methods and overall women's health management.

Interventions

OTHERNo intervention

No intervention

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* They should be virgin, healthy female physiotherapy students with PD. * They have regular menstruation (3-8 days in duration, with 21-35 days in between). * Their ages will range from 18 to 25 years old. * Their body mass index (BMI) will range from 18 to 24.9 kg/m2. * Their waist-to-hip ratio will be less than 0.8.

Exclusion criteria

* Any urological or gynecological disorders in the previous 12 weeks (e.g., endometriosis, fibroids). * Fibromyalgia. * Severe psychiatric or psychological disorders. * Those who had taken analgesics in the 12 hours before the assessment. * Abdominal or pelvic surgery within the past six months.

Design outcomes

Primary

MeasureTime frameDescription
Pelvic floor muscle (PFM) contraction1 monthTransabdominal ultrasound (TAU) will be used to assess PFM contraction for all females (cutting off the flow of urine mid-stream) in the three groups.
Pelvic floor muscle (PFM) relaxation1 monthTransabdominal ultrasound (TAU) will be used to assess PFM relaxation during inspiration for all females.

Secondary

MeasureTime frameDescription
Bladder section of the Australian Pelvic Floor Questionnaire1 monthIt will be used to assess the bladder symptoms of pelvic floor dysfunction for all females in the three groups. This section will be scored 0-45, with higher scores meaning more dysfunction
Bowel section of the Australian Pelvic Floor Questionnaire1 monthIt will be used to assess the bowel symptoms of pelvic floor dysfunction for all females in the three groups. This section will be scored 0-34, with higher scores meaning more dysfunction
36-Item Short Form Survey Instrument (SF-36)1 monthThe SF-36 questionnaire is a self-administered questionnaire containing 36 items. It measures health across eight multi-item dimensions, covering functional status, well-being, and overall health evaluation, each associated with 2-10 possible answers. The response to each question is extrapolated to a standardized set of answers, and the results are transferred to a scale of 0-100, where 0 represents the worst state of health and 100 represents the best state of health measured

Countries

Egypt

Contacts

Primary ContactWafaa AM Abdelraouf, B.Sc.
wafaaabdelraouf12@gmail.com01021080497
Backup ContactAmira Nagy Abdellatif, PhD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026