Exercise, Motor Imagery, and Pain Neuroscience Education for Primary Dysmenorrhea: A Randomized Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-25
SponsorMuge Dereli

About this trial

The goal of this clinical trial is to find out whether exercise, motor imagery training, and pain neuroscience education can help reduce menstrual pain and improve well-being in young women with primary dysmenorrhea. The study will also look at how these approaches affect menstrual symptoms, movement control, and cognitive flexibility.

The main questions it aims to answer are:

* Does adding motor imagery or pain neuroscience education to an exercise program reduce pain and menstrual symptoms more than exercise alone? * Do these approaches improve movement control, thinking flexibility, and knowledge about pain?

Researchers will compare three groups:

* Exercise only * Exercise plus motor imagery training * Exercise plus pain neuroscience education

Participants will:

* Attend supervised exercise sessions twice a week for 8 weeks * Practice either motor imagery or receive short pain neuroscience education, depending on their group * Complete questionnaires and tests before and after the program, during the first three days of menstruation

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female, aged 18-25 years

Gynecological examination and ultrasound confirming absence of pelvic pathology

History of primary dysmenorrhea for at least 6 months, with pain intensity ≥4 on the Numeric Rating Scale (0-10) during the first 3 days of menstruation

Regular menstrual cycles (21-35 days)

Disqualifiers

Diagnosis of secondary dysmenorrhea (e.g., endometriosis, pelvic inflammatory disease, uterine fibroids, ovarian cysts)

Current pregnancy or planning to become pregnant during the study period

History of pelvic or abdominal surgery

History of sexually transmitted diseases

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exercise Program

    Behavioral

    Participants will complete an 8-week supervised exercise program, delivered twice per week. The program includes lumbopelvic stabilization, stretching, and endurance training exercises designed to reduce menstrual pain and improve physical function.

  • Exercise plus Motor Imagery Training

    Behavioral

    Participants will complete the same 8-week supervised exercise program as the Exercise Only group. In addition, they will practice kinesthetic motor imagery of the prescribed movements prior to performing them, aiming to enhance motor control and pain modulation.

  • Exercise plus Pain Neuroscience Education

    Behavioral

    Participants will complete the same 8-week supervised exercise program as the Exercise Only group. In addition, they will receive weekly face-to-face pain neuroscience education sessions focused on pain neurophysiology, supported with home assignments to reinforce learning.

Treatment groups

51 Participants
are divided into 3 treatment groups
Group A: Exercise OnlyExperimental treatment 1 intervention
Group B: Exercise + Motor ImageryExperimental treatment 2 interventions
Group C: Exercise + Pain Neuroscience EducationExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Pain Intensity

Pain intensity will be assessed using an 11-point Numeric Rating Scale (0 = no pain, 10 = worst imaginable pain). Participants will be asked to report their average menstrual pain during the first three days of menstruation.

Time frame
Baseline, after 8 weeks of intervention, and 1 month post-intervention follow-up
2

Pressure Pain Threshold (PPT)

Pressure pain threshold will be measured using a digital algometer (Baseline dolorimeter) applied to the abdominal region and standardized body sites. The minimum pressure (kg/cm²) at which pain is first perceived will be recorded.

Time frame
Baseline and after 8 weeks of intervention (first three days of menstruation)
3

Menstrual Symptom Severity

Menstrual symptoms (e.g., cramps, headache, back pain, fatigue, mood changes) will be evaluated using the Menstrual Symptom Questionnaire (MSQ). Total and subscale scores will be calculated.

Time frame
Baseline, after 8 weeks of intervention, and 1 month post-intervention follow-up

Secondary outcomes

1

Lumbopelvic Motor Control

Lumbopelvic motor control will be assessed using the Physioupplies Core Stabilizer Unit, which measures pressure changes during standardized stabilization tasks.

Time frame
Baseline and after 8 weeks of intervention
2

Movement Imagery Ability

Participants' ability to generate and control movement imagery will be assessed using the Movement Imagery Questionnaire. Higher scores indicate better imagery ability.

Time frame
Baseline
3

Central Sensitization

Central sensitization symptoms will be evaluated using the Central Sensitization Inventory (CSI). The total score reflects symptom severity.

Time frame
Baseline, after 8 weeks of intervention, and 1 month post-intervention follow-up
4

Cognitive Flexibility

Cognitive flexibility and inhibitory control will be assessed using the EncephalApp Stroop application. Participants will complete the "off" and "on" runs. Primary variables will be total completion time (seconds) and error count; lower times and fewer errors indicate better performance.

Time frame
Baseline and after 8 weeks of intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Muge Dereli

Lead sponsor

Izmir Katip Celebi University

Sponsor institution