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Clinical Trials in Turkey / NCT06860256
Starting soon Not applicable

Different Exercise Training Programs in University Students with Primary Dysmenorrhea

NCT06860256 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-02-25
Last updated
2025-03-06

Condition(s) studied

ExercisePrimary Dysmenorrhea

Investigational drug(s) / intervention(s)

Basic Body Awareness TherapyHigh Intensity Interval TrainingClassic Exercise and Lifestyle Tips

Basic Body Awareness Therapy: In TBFT sessions, physiotherapists improve the patient's contact with "self" by focusing on basic movement principles while performing simple daily movements such as lying, sitting, standing, walking, use of sound and massage. Mental awareness, postural balance and free breathing are considered key elements. The patient is invited to explore and integrate flow, rhythm and intentionality in coordinated movements in relation to time, space and energy. TBFT is practiced 2 days a week, 60 minutes, 5-12 weeks, depending on the patient.

High Intensity Interval Training: Tabata exercise protocol is an 8 repetition training program with 20 seconds of work and 10 seconds of rest. Warm-up and cool-down exercises of 5 minutes each should be done to prevent injuries and negativities. Although the application varies according to the patient, YŞİA is applied 2 days a week, 15-30 minutes, in processes ranging between 2-12 weeks.

Classic Exercise and Lifestyle Tips: Classical Exercise (CE) and Lifestyle Recommendations (LSR), Classical exercises used in PD include abdominal, pelvic floor muscles, hip flexors, whole body stretching. Non-pharmaceutical strategies for pain management in LRS include adopting relaxation (rest, warm-up, massage, music, etc.), antalgic positions, and distraction techniques. Common techniques that facilitate relaxation and thus reduce pain include physical rest, hot showers, various heat applications such as thermal seed bags, electric blankets, and drinking hot herbal teas such as chamomile tea.

Study summary

Dysmenorrhea is severe lower abdominal pain in women during menstruation. The pain is usually cramping and can radiate to the thighs or lower spine. Lower abdominal pain may be accompanied by vomiting, headache, back pain, diarrhea, fatigue, etc. Depending on the pathophysiology, dysmenorrhea is classified into two types: primary and secondary. Primary dysmenorrhea (PD) is menstrual pain associated with normal ovulatory cycles in the absence of pelvic pathology and a clear physiologic etiology and is most commonly seen in adolescents and young adults. There are numerous studies on PD in the literature, but there is still a lack of studies on which of the non-pharmacologically recommended exercise and other methods is more effective on dysmenorrhea symptoms, sleep and quality of life for individuals with this problem. Different exercise intensities may affect PD symptoms through different mechanisms. Moderate to high intensity exercise may reduce pain by increasing anti-inflammatory cytokines, whereas less intense exercise, such as yoga, affects pain levels by decreasing cortisol levels. The lack of research on which exercise training is more effective in PD individuals was considered as a limitation. In the light of this information, the aim of the investigators study is to compare the effects of different training techniques on dysmenorrhea symptoms, sleep and quality of life in PD treatment and to present the preferability of these techniques based on evidence.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Nulliparous female university students aged 18-25 years who volunteered to participate in the study, met the criteria specified in the PD Consensus Guidelines and were diagnosed with PD by a gynecologist * Individuals with a body mass index (BMI) between 18-35 * Individuals with a regular menstrual cycle (28 ± 7 days) * Individuals with menstrual pain Visual Analog Scale (VAS) score of 4 cm or higher for the last 6 months Exclusion Criteria: * Gastrointestinal, urogynecologic, autoimmune, psychiatric, neurological diseases or other chronic pain syndromes * Having given birth and/or being pregnant * Intrauterine device users * Pelvic surgery patients * Taking oral contraceptives or medication, including antidepressants, for at least 6 months before the study * Those with a pathological history or ultrasonography result indicating secondary dysmenorrhea * Those who use alternative treatment methods and exercise regularly * Serious traumatic life events that occurred in the three months prior to the start of the study * Communication problems that may interfere with the implementation of assessments and/or treatment program

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kilis 7 Aralık University Kilis Province

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06860256 on ClinicalTrials.gov ↗ ← All trials in Turkey