Effect of Yoga Training on Nausea and Pain

NCT ID: NCT07000487

Last Updated: 2025-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-01

Study Completion Date

2025-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study was planned to determine the effect of yoga training on reducing nausea and pain symptoms in young women with primary dysmenorrhea. As a result of this study, evaluating the extent to which women with dysmenorrhea experience pain and nausea and the extent to which yoga has a positive effect on these symptoms may shed light on women experiencing these symptoms and developments in the literature, and may increase the use of non-pharmacological approaches. The results of the study will contribute to the literature on dysmenorrhea, one of the important gynecological problems in women. In addition, although there are many results in the literature on the effectiveness of yoga in the management of nausea symptoms with cancer patients, there are not many studies on nausea on dysmenorrhea. In this respect, it will provide important evidence to the literature.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Primary dysmenorrhea (PD) is one of the most common gynecological conditions affecting an estimated 67% to 90% of young women and is a painful uterine contraction caused by endometrial laceration . PD is also known as painful periods or menstrual cramps that cause pain during the menstrual cycle. Menstrual pain is the most common symptom associated with primary dysmenorrhea. The pathogenesis of menstrual pain is thought to be due to an abnormal increase in the production of vasoactive prostaglandins in the endometrium, which can induce myometrial hyperactivity, uterine tissue ischemia, and pain. The pain caused by dysmenorrhea begins a few days before menstruation and lasts for 48-72 hours. The pain is usually in the pelvis or lower abdomen and may radiate to the lower back and upper thighs. Other symptoms that the individual may experience include diarrhea, headache, stress, and nausea.

Yoga is one of the self-development and exercise methods that fully trains the soul, mind and body and allows the individual to know themselves. Yoga, which is a mental journey that the individual makes to their inner world, is a technique that allows the person to be alone with themselves as a result of the combination of physical posture, breathing techniques and mental meditation. The yoga-based lifestyle includes positive behavioral changes (yamas and niyamas), physical posture practices (asanas), breathing regulation (pranayama), control of the senses (pratyahara) and meditation techniques (dharana, dhyana and samadhi). It has been determined in the literature that yoga reduces menstrual cramps and distress, and it has been reported that it can be used in menstrual problems due to its safety, lack of side effects, low cost, easy accessibility and noninvasiveness. Previous studies report that yoga suppresses menstrual pain by reducing the level of prostaglandin production and myometrial ischemia through "down-regulation of the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system" and has positive effects on psychological well-being. In addition, studies have determined that yoga is also effective in nausea and vomiting symptoms. In a systematic review conducted on individuals with cancer, it was determined that yoga is effective in symptom management (nausea and vomiting, fatigue, anxiety, depression, etc.). The aim of this study is to determine the effect of yoga training in reducing nausea and pain symptoms in young women with primary dysmenorrhea. The results of the study will contribute to the literature on dysmenorrhea, one of the important gynecological problems in women. In addition, although there are many results in the literature on the effectiveness of yoga in the management of nausea and vomiting symptoms with cancer patients, no study on dysmenorrhea has been found. In this respect, it will also provide important evidence to the literature.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Primary Dysmenorrhea (PD) Yoga

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study consists of two groups: control and experimental group.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Since the application will be performed by the researcher, patients will be blinded in this study. The statistician will be blinded in the evaluation of the data.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Experimental:Yoga

Hatha yoga will be applied in this study. Yoga practice will be carried out by the researcher for 6 weeks, 1 day face-to-face and 1 day online, and each practice will be 60 minutes, in total 12 sessions, considering the studies done. It will be applied by a researcher with a yoga certificate. Pre-test and post-test nausea and pain measurements will be made.

Group Type EXPERIMENTAL

Yoga

Intervention Type BEHAVIORAL

Hatha yoga will be applied in this study. Yoga practice will be carried out by the researcher for 6 weeks, 1 day face-to-face and 1 day online, and each practice will be 60 minutes, in total 12 sessions, considering the studies done. It will be applied by a researcher with a yoga certificate. Pre-test and post-test nausea and pain measurements will be made.

No Intervention: Control Group

No application will be made to this group by the researcher.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Yoga

Hatha yoga will be applied in this study. Yoga practice will be carried out by the researcher for 6 weeks, 1 day face-to-face and 1 day online, and each practice will be 60 minutes, in total 12 sessions, considering the studies done. It will be applied by a researcher with a yoga certificate. Pre-test and post-test nausea and pain measurements will be made.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Having a regular menstrual cycle
* Being single
* Not having any psychiatric diagnosis or gynecological disease (abnormal uterine bleeding, myoma, ovarian cysts, etc.) extremities and any health problems that may prevent physical exercise
* Not having any systemic disease (heart, diabetes, epilepsy, rheumatoid arthritis, etc.)
* Young women who agree to participate in the study and can speak and understand Turkish

Exclusion Criteria

* Wanting to leave the study, primary dysmenorrhea severity and nausea level below 4 points.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Çankırı Karatekin University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Sakine Yılmaz

Assistant Professor Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Çankırı

Çankırı, None Selected, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Sakine Yılmaz

Role: CONTACT

05439380626

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Sakine Yılmaz, Assistant Professor Doctor

Role: primary

+905439380626

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Primary dysmenorrhea

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.