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Primary DysmenorrheaNCT06984003

Pulsed Electromagnetic Field Versus Active Stretching Exercises on Primary Dysmenorrhoea Randomized Controlled Study

A study testing stretching exercises in people with Primary Dysmenorrhea, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Primary dysmenorrhea (PD) refers to painful cramps before and/or during menstruation. There is a need for emphasis on alternative methods of conservative treatment, so as to reduce the dependence on drugs for alleviating the symptoms., so the aim of this study was to investigate the effect of pulsed electromagnetic… Read more about this study

Who is it for?
Ages 18 to 24 years, women only
Conditions the study is for
Primary Dysmenorrhea
What is being tested?
stretching exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteEgypt
Study dates
30 May 2025to 1 Jul 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 24 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Young female students suffering from primary dysmenorrhea
  • regular menstrual cycle diagnosed by gynecologist
  • BMI ranging from 18.5 to 25 kg/ m 2.
  • Pain intensity is 4 or above in VAS.
  • Their ages ranged from 18- 24 years old-

Who cannot join

  • Girls with irregular or infrequent menstrual cycles, using pharmacological or non-pharmacological methods for pain relief during the study
  • suffering from pelvic pathology

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Faculty of Physical Therapy, Cairo University.

    Cairo, 12518

Other trials in Egypt

About this study

Official title: Efficacy of Pulsed Electromagnetic Field Versus Active Stretching Exercises on Primary Dysmenorrhea

Primary dysmenorrhea (PD) refers to painful cramps before and/or during menstruation. There is a need for emphasis on alternative methods of conservative treatment, so as to reduce the dependence on drugs for alleviating the symptoms., so the aim of this study was to investigate the effect of pulsed electromagnetic field versus active Stretching exercises on primary dysmenorrhea.

Read the detailed description

Dysmenorrhea is a menstrual disorder characterized by suprapubic cramping of uterine origin and pain occurring a few hours before or after the onset of menstruation. Primary dysmenorrhea begins when young girls experience the first menstrual adulatory cycles, and its prevalence increases during adolescence (15-17 years) and reaches its highest at 20-24 years and decreases progressively thereafter. Primary dysmenorrhea is characterized by abdominal pain, beginning a few hours before and continuing up to 12-72 hours, and is like the delivery of pains along with cramps in the lower abdomen radiating toward the inner side of the thighs. Half of such cases experience systemic symptoms, such as nausea, vomiting, diarrhea, fatigue, irritability, and dizziness.

Primary dysmenorrhea occurs in up to 50% of menstruating females and causes significant disruption in quality of life.4 Menstrual cramps are associated with nausea in 55% and with vomiting in 24%.5 The severity of symptoms positively correlates with the onset of ovulatory cycles and with increased duration and amount of menstrual flow.6 A physiological reason for dysmenorrhea is the production of uterine prostaglandins. During endometrial sloughing, endometrial cells release prostaglandins as menstruation begins. Prostaglandins stimulate myometrial contractions and ischemia.7 During the recent 20-30 years, regular exercise and physical activities have been introduced as effective methods for prevention and treatment of dysmenorrhea.8Exercising affects the levels of steroid hormones in the blood circulation of women in reproductive ages.9 Moreover, the elevation of the endorphin hormone leads to an increase in pain threshold.10 Pulsed electromagnetic field (PEMF) is an efficient modality used in physical therapy field for treatment of many pathological cases; PEMF has strong analgesic effect, anti-inflammatory effect, and a vasodilatation effect, as well as decreasing edema.11 PEMF has electric energy and generates series of magnetic pulses through the tissues, and each magnetic pulse induces a tiny electrical signal that stimulates cellular repair, suppresses inflammatory responses, alleviates pain, and increases range of motion.12 PEMF are effective in relieving pain of primary dysmenorrhea by decreasing prostaglandin levels in the blood, resulting in fewer vigorous uterine contractions and less discomfort.

A range of treatment options have been examined in the literature, including heat application, pelvic floor and aerobic exercises, low-level laser therapy, and pulsed electromagnetic field, with several producing effective outcomes. These interventions were assumed to prevent or minimize menstrual pain by increasing pelvic circulation, decreasing uterine contractions, and activating the release of endorphins and serotonin, but there is still no evidence for the best type of modality chosen.

Additional researches are needed to clarify difference between effect of Pulsed electromagnetic field (PEMF) and active stretching on pain intensity level and menstrual symptoms in females with primary dysmenorrhea.

Being tested
stretching exercises
Keywords
Primary Dysmenorrhea, Pulsed Electromagnetic Field, Active Stretching Exercises

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • stretching exercisesOther

    a brief explanation, by a trained physical therapist, of stretching exercise program and of how to practice these active stretching exercises as a home program 3 times per week for 4 weeks.

Study groups in NCT06984003
Study groupRoleWhat they receive
pulsed electromagneticExperimentalThe magnetotherapy device (level s.r.l. SEDE LEGALE, Catania, Italia) consists of the control panel, motorized bed, and two solenoids (52 cm in diameter for the stand and 80 cm in diameter for the bed). The control panel is connected to electrical mains, supplying 230 V AC 50 Hz. graphic display, multifunction control with encoder selection through a MENU SUBMENU, making the machine easy to use. Pillows and cushions were used to support body parts in a comfortable, relaxed position, and sheets were used to cover the patients during treatment sessions. Participants randomly assigned into Group A (n = 15) received PEMF applied to the pelvic region 3 days per week for 8 weeks, twenty minutes per day. The used parameters of PEMF were 50 Hz in frequency and 60 G in intensity applied in the comfortable supine lying position with small pillows under the participants' body curves.
Receives: Other: stretching exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. pain intensity assessment in primary dysmenorrhea

    by using a visual analogue scale (VAS) was performed before and after the treatment. VAS is a self-reported 10-cm straight line, which represents the pain intensity, with the two opposite ends representing no pain and worst pain. Based on the VAS scale, those subjects with pain intensity of 4 to 7 were classified as the moderate group. The subjects with a pain score between 7 and 10 were considered to have a severe form of dysmenorrhea. The subjects with pain intensity less 4 were excluded from the research design. Each participant was asked to place a mark along the line to denote the level of pain

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 May 2025
  2. Study start30 May 2025
  3. Primary completion15 Jun 2025
  4. Study completion1 Jul 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06984003
Sponsor's protocol ID
(P.T. REC/012/005704)
Status last verified
Jul 2025
First submitted
14 May 2025
Last updated
30 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing stretching exercises in people with Primary Dysmenorrhea, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

pain intensity assessment in primary dysmenorrhea (time frame: 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jul 2025.

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