Evaluation of the Effect of a Structured Yoga Exercise in Young Women With Primary Dysmenorrhea
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Yoga Exercise Program.
- Who it may be relevant to
- Registry conditions: Primary Dysmenorrhea. Basic parameters: 18 years — 25 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of the Effect of a Structured Yoga Exercise Program on Pain, Menstrual Symptoms, and Quality of Life in Young Women With Primary Dysmenorrhea
Overview
Abstract Primary dysmenorrhea is a common gynecological condition affecting women of reproductive age and negatively impacting quality of life. It is characterized by cramping pain in the lower abdomen that may radiate to the lower back and thighs, leading to decreased daily functioning, academic performance, and psychological well-being. In addition to pharmacological treatments, complementary approaches are increasingly used in the management of dysmenorrhea. Yoga, a mind-body exercise that combines physical movement with mental focus, has been suggested as an effective method for reducing stress and pain associated with dysmenorrhea. The aim of this study is to evaluate the level of awareness about dysmenorrhea in young women with primary dysmenorrhea and to investigate the effects of a yoga program on pain, quality of life, and menstrual attitudes following an educational session provided to all participants. Pain severity, quality of life, and menstrual attitudes will be assessed using validated questionnaires and scales, including the Visual Analog Scale (VAS), awareness questionnaire, functional and emotional dysmenorrhea scale, Menstrual Attitude Scale, and quality of life questionnaire. This study aims to determine whether yoga exercises reduce dysmenorrhea symptoms and improve quality of life in young women with primary dysmenorrhea. Additionally, the study is expected to increase awareness about dysmenorrhea and provide evidence for the effectiveness of yoga as a non-pharmacological intervention.
Detailed description
This study aims to evaluate the effects of yoga exercise on dysmenorrhea symptoms in young women with primary dysmenorrhea. Additionally, the study aims to examine the effects of yoga exercises on participants' quality of life. Although dysmenorrhea is highly prevalent among young women, the use of non-pharmacological approaches for its management is considered limited. Therefore, a structured yoga exercise program will be applied to the participants in this study.
Pain intensity, quality of life, and menstrual attitudes of the participants will be evaluated. During the data collection process, Personal Information Form, Visual Analog Scale (VAS), Functional and Emotional Dysmenorrhea Scale, Menstrual Attitude Scale, and quality of life questionnaire will be used. Assessments will be performed before and after the exercise program.
This study aims to determine whether a yoga exercise program is effective in reducing pain and improving quality of life in young women with primary dysmenorrhea.
Interventions
- Other Yoga Exercise Program
Participants in the intervention group will receive a structured yoga exercise program. The yoga program will include breathing exercises, relaxation techniques, and selected yoga postures targeting the pelvic region. The exercises will be performed regularly for the duration of the study. Pain intensity, quality of life, and menstrual attitudes will be evaluated before and after the intervention.
Primary outcome measures
- Pain intensity (VAS) [Time frame: Baseline and immediately after the 8-week intervention]
Secondary outcome measures (4)
- Secondary Outcome Measure: Participant Experiences [Time frame: after 8 weeks of intervention]
- Functional and Emotional Dysmenorrhea Scale [Time frame: baseline and after 8 weeks of intervention]
- Health-Related Quality of Life [Time frame: Baseline and Week 8]
- Menstrual Attitudes [Time frame: Baseline and Week 8]
Eligibility criteria
Inclusion criteria
- Healthy young women with primary dysmenorrhea
- Aged between 18-25 years
- Having a regular menstrual cycle (30-35 days)
- Menstrual bleeding duration of 3-10 days
Exclusion criteria
- Having secondary dysmenorrhea
- Participation in regular physical activity or other exercise programs
- Use of medication
- Diagnosed with polycystic ovary syndrome
- Having bleeding disorders
- Positive pregnancy test
- Being in the breastfeeding period
- Primary dysmenorrhea attributed to medical disorders or other causes
- Participants who miss three consecutive sessions or four alternating sessions during the study will be excluded from the research
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Ankara University, Haymana Vocational School — Ankara
Identifiers
NCT: NCT07520136 · YOGA52U