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NCT Number: NCT07095725

Effect of Primary Dysmenorrhea on Muscle Activity in Young Adult Females

This study aims to investigate the effect of primary dysmenorrhea on the activity of the abdominal and back muscles in young adult females.

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Key information

Age range

18 year–25 year

Sex eligibility

Female

Study type

Observational

Primary location

Misr University for Science and Technology

Giza, Egypt

Location status: Recruiting

Location contact

Mahenour Esmail Shendy, Bachelors of Physical Therapy

CONTACT

[email protected]

01112129932

About this study

PD is highly prevalent in females, which directly influences their quality of life, physical function and performance. A study conducted in Palestine has shown that over half of university students with dysmenorrhea tend to skip university lectures due to painful menses.

PD is commonly associated with visceral pain and various musculoskeletal symptoms, including abdominal and back pain (Yacubovich et al., 2019). This can reduce the maximum voluntary contraction of the affected muscles, compromising their ability to provide adequate support and stability (Merkle et al., 2020). Persistent pain can disrupt postural stability and balance, raising the risk of injury by compromising stability and muscle function.

Research highlights the impact of primary dysmenorrhea (PD) on muscle function, particularly in the abdominal and back muscles, contributing to pain and reduced stability. Oladosu et al. (2018) found that abdominal muscle activity precedes menstrual pain, suggesting a neuromuscular link. Similarly, Karakus et al. (2022) and Álvarez et al. (2024) reported altered activation and reduced endurance in stabilizing muscles, including the transversus abdominis, obliques, and lumbar multifidus, with muscle thinning that may impair spinal stability. These studies emphasize PD's effect on muscle function, but further research is needed to explore variations across severities and guide effective treatments.

When these weakened muscles because of dysmenorrhea are subjected to increased or sudden activity during daily living tasks, such as lifting, bending, or other physical exertions, the risk of injury to the structures they are designed to protect is significantly heightened (Escamilla et al., 2010; Polat et al., 2022).

However, to the best of the authors' knowledge, no research has yet explored the relationship of abdominal and back muscle activity patterns to PD and their variations across different severities of dysmenorrhea, which directly contributes to females' quality of life.

Understanding this association could have significant clinical implications and contribute to new knowledge that helps physical therapists determine the need for custom-designed prevention and treatment programs for females with PD. By raising awareness of the potential musculoskeletal risks associated with PD, this study emphasizes the importance of minimizing strenuous activities during menstruation to reduce muscle strain or injury, ultimately enhancing overall health and well-being during this period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All females clinically diagnosed with PD, as confirmed and referred by a gynecologist.
  • Age ranges from 18 to 25 years.
  • BMI ranges from 20 to 25 kg/m2 .
  • Onset of menstrual pain 6-24 months after menarche.
  • Having a regular menstrual cycle (28 ± 7 days with no intermittent bleeding).
  • Their PD symptoms will be determined according to the WaLLID questionnaire and will be classified into mild PD (1-4), moderate PD (5-7), severe PD (8-12).
  • All participants are virgins.

Exclusion criteria

  • Menstrual irregularity.
  • Use of antidepressant or steroid drugs.
  • Secondary dysmenorrhea.
  • Musculoskeletal problems in the abdominal region, pelvic region, or spine.
  • Surgical history involving the abdominal region, pelvic region, or spine in the last year.
  • Any psychiatric or gynecological problems.

Treatment and study plan

Record EMG maximum amplitude from rectus abdominis, erector spinae L3 level

Diagnostic Test

EMG Electrode Placement and Muscle Assessment:

Electrodes for the rectus abdominis were placed longitudinally at the umbilical level. For the erector spinae, L3 was located using a line between the posterior superior iliac crests, and electrodes were placed ~3 cm lateral to the L3 spinous process.

Assessment:

Rectus Abdominis: In the crook-lying position, participants performed a slow curl-up (~35-40°), holding for 10 seconds.

Erector Spinae: In the prone position with a 10-cm pad under the abdomen, participants lifted the upper body with neutral cervical alignment for 10 seconds.

Each test was repeated three times with 2-minute rest intervals.

Primary outcomes

  1. Activity of rectus abdominis muscle

    Time frame: 3 months

    Maximum voluntary contraction in (μV) of rectus abdominis using electromyography device (EMG)

  2. Activity of erector spinae muscle at L3 vertebrae Level

    Time frame: 3 Month

    Maximum voluntary contraction in (μV) of erector spinae at L3 Level using electromyography device (EMG)

Study contacts

Contact information is provided by the study sponsor or research team.

Abdelrahman Salah Sawan, Bachelor of Physical Therapy

CONTACT

[email protected]

01144047770

Mahenour Esmail Shendy, Bachelor of Physical Therapy

CONTACT

[email protected]

01112129932

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jul 31, 2025
Registry last updated
Aug 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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