Actively Recruiting

Age: 18Years - 25Years
FEMALE
ID07095725

Effect of Primary Dysmenorrhea on Abdominal and Back Muscles Activity in Young Adult Females

Led by Cairo University · Updated on 2025-08-05

72

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how primary dysmenorrhea (PD), a common condition causing painful menstrual cramps, affects the activity of abdominal and back muscles in young adult females aged 18 to 25 years. PD is linked to reduced muscle strength and stability, leading to pain and higher injury risk during daily activities. This study aims to better understand muscle activity changes across different PD severities to guide prevention and treatment strategies. Participants will be grouped by PD severity based on the WaLLID scale into mild, moderate, and severe categories. Muscle activity will be assessed using electromyography (EMG) by placing electrodes on the rectus abdominis and erector spinae muscles. Tests include slow curl-ups and upper body lifts held for 10 seconds each, repeated three times with rest periods. The study is observational and focuses on evaluating muscle function without administering treatments. During the 3-month study, participants will undergo muscle activity assessments to measure rectus abdominis and erector spinae function. Researchers will analyze these measurements to understand the muscle activity patterns related to PD severity. The study also collects clinical data and questionnaires about menstrual pain. The outcome will help physical therapists design tailored programs to improve muscle support and reduce injury risk in females with PD.

CONDITIONS

Brief Title

Effect of Primary Dysmenorrhea on Muscle Activity in Young Adult Females

Who Can Participate

Age: 18Years - 25Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female individuals clinically diagnosed with primary dysmenorrhea, confirmed by a gynecologist.
  • Age between 18 and 25 years.
  • Body mass index (BMI) between 20 and 25 kg/m2.
  • Onset of menstrual pain 6 to 24 months after menarche.
  • Regular menstrual cycle lasting 28 �b1� 7 days with no intermittent bleeding.
  • PD symptoms classified by WaLLID scale into mild (1-4), moderate (5-7), or severe (8-12).
  • All participants are virgins.
Not Eligible

You will not qualify if you...

  • Irregular menstrual cycles.
  • Use of antidepressant or steroid medications.
  • Diagnosis of secondary dysmenorrhea.
  • Musculoskeletal problems in the abdominal, pelvic, or spine regions.
  • Surgical history involving abdominal, pelvic, or spine areas within the past year.
  • Any psychiatric or gynecological disorders.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Single assessment session

Participants undergo EMG assessments to record maximum muscle activity from the rectus abdominis and erector spinae muscles during specific muscle contractions.

1 visit (in-person)

Long-term Monitoring

Duration - 3 months

Participants' muscle activity and dysmenorrhea symptoms are observed over a 3-month period to understand muscle function variations across different severities of primary dysmenorrhea.

Follow-up visits as scheduled over 3 months

Trial Site Locations

Total: 1 location

1

Misr University for Science and Technology

Giza, Egypt

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Research Team

M

Mahenour Esmail Shendy, Bachelor of Physical Therapy

A

Abdelrahman Salah Sawan, Bachelor of Physical Therapy

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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