Myofascial Release Technique in Women With Primary Dysmenorrhea

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-35
SponsorGazi University

About this trial

It has been found that women with dysmenorrhea have active trigger points, particularly in the rectus abdominis, oblique abdominal muscles, quadratus lumborum, and paraspinal muscles. The myofascial release technique is a widely used manual therapy method characterized by the application of low-load, long-duration mechanical forces to manipulate the myofascial complex. This technique aims to restore optimal length, alleviate pain, and improve function. This study aims to examine the effect of the myofascial release technique on central sensitization, myofascial trigger points, and menstrual symptoms in women with primary dysmenorrhea.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed with Primary Dysmenorrhea according to the Primary Dysmenorrhea Consensus Guide,

Having regular menstruation in the last 6 months (28±7 days)

Those who had menstrual pain between 40 mm and 100 mm according to the Visual Analogue Scale (VAS) in the last 6 months

Disqualifiers

Diagnosed with Secondary Dysmenorrhea,

Having given birth,

Those with serious gastrointestinal, urogynecological, or autoimmune diseases or other chronic pain syndromes,

Undergoing urogynecological surgery,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Myofascial Release

    Other intervention

    The myofascial release technique is a widely used manual therapy method characterized by low-load, prolonged mechanical forces applied to manipulate the myofascial complex, aiming to restore optimal length, alleviate pain, and improve function.

  • Sham-Myofascial Release

    Other intervention

    The hands of the researcher applying the technique will be placed in the same areas as the myofascial release technique, with only the palms in light contact for the same duration. However, no intervention will be made to create any pressure or open the tissue barrier.

Treatment groups

36 Participants
are divided into 2 treatment groups
Group A: Myofascial Release GroupActive comparator 1 intervention
Group B: Sham- Myofascial Release GroupSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain Pressure Threshold

Trigger points in specific muscles (rectus abdominis, paraspinal muscles, quadratus lumborum, gluteus maximus) will be determined. Then, it will be applied to the trigger points with the Baseline brand algometer in accordance with standard procedures and the pressure will be increased by 30 kPa/s.

Time frame
Baseline (First menstruation cycle)
2

Pain Pressure Threshold

Trigger points in specific muscles (rectus abdominis, paraspinal muscles, quadratus lumborum, gluteus maximus) will be determined. Then, it will be applied to the trigger points with the Baseline brand algometer in accordance with standard procedures and the pressure will be increased by 30 kPa/s.

Time frame
through study completion, an average of 3 months
3

Central Sensitization

Pain threshold will be measured with an algometer at a certain point of the tibialis muscle.

Time frame
Baseline (First menstruation cycle)
4

Central Sensitization

Pain threshold will be measured with an algometer at a certain point of the tibialis muscle.

Time frame
through study completion, an average of 3 months

Secondary outcomes

1

Menstrual Attitude

Menstrual Attitude Scale will be used to evaluate symptoms related to menstruation. High scores indicate a high awareness of menstruation.

Time frame
Baseline (First menstruation cycle)
2

Menstrual Attitude

Menstrual Attitude Scale will be used to evaluate symptoms related to menstruation. High scores indicate a high awareness of menstruation.

Time frame
through study completion, an average of 3 months
3

Health-related quality of life

Short Form (SF-36) will be used to evaluate individuals' general health-related quality of life. SF-36 is a 36-question survey that evaluates functionality and well-being and consists of 8 subscales. Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively. Higher scores indicate a better quality of life.

Time frame
Baseline (First menstruation cycle)
4

Health-related quality of life

SF-36 will be used to evaluate individuals' general health-related quality of life. SF-36 is a 36-question survey that evaluates functionality and well-being and consists of 8 subscales. Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively. Higher scores indicate a better quality of life.

Time frame
through study completion, an average of 3 months

Other outcomes

Sponsors and contacts

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