The Effect of Laughter Yoga and Premenstrual Symptoms
The Effect of Laughter Yoga on Quality of Life and Premenstrual Symptoms in Young People With Premenstrual Syndrome: A Randomized Controlled Experimental Study
1 other identifier
interventional
75
1 country
1
Brief Summary
Premenstrual Syndrome (PMS) describes somatic, cognitive, emotional, and behavioral symptoms that occur in women during the luteal phase of the menstrual cycle and resolve with the onset of menstruation. These symptoms are common during the reproductive years. The emotional symptoms of PMS include depression, outbursts of anger, irritability, crying spells, anxiety, confusion, social withdrawal, poor concentration, insomnia, increased short sleep, and changes in sexual desire. Premenstrual symptoms negatively impact women's relationships with family, work, and friends, as well as their social activities. Furthermore, premenstrual symptoms negatively impact a woman's quality of life, making them an important issue to address early in a woman's life. Numerous treatment methods are used to reduce or eliminate PMS symptoms. Laughter yoga is one of the alternative medicine methods that has recently emerged and is used to maintain and improve health. No studies have examined the effectiveness of laughter yoga in reducing premenstrual syndrome. This study aims to determine the effects of laughter yoga on quality of life and premenstrual symptoms in young people experiencing premenstrual syndrome.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 10, 2025
CompletedFirst Posted
Study publicly available on registry
July 20, 2025
CompletedStudy Start
First participant enrolled
December 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2025
CompletedJanuary 27, 2026
January 1, 2026
Same day
July 10, 2025
January 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
The Premenstrual Symptoms Coping Scale
This scale assesses the coping with premenstrual symptoms in women aged 18-49. The scale consists of 27 items and five subscales in Turkish. Each item on this five-point Likert-type scale is scored from one to five. The total score is not used.
between 2 to 4 weeks
Premenstrual Syndrome-Specific Quality of Life Scale
The scale consists of 22 items divided into three subscales: physical, emotional, and social. Reverse coding is used for all items, with a minimum score of 22 and a maximum score of 110.
between 2 to 4 weeks
Study Arms (2)
Laughter yoga group
EXPERIMENTALBefore starting the intervention, the researcher attended a 12-hour "Laughter Yoga Leader" course (8 hours of theory and 4 hours of Laughter Yoga Practice). Following the course, the researcher received a "Laughter Yoga" certificate. In the first stage, all participants will be asked to introduce themselves by giving their names and places of birth. Then, laughter yoga will begin with warm-up exercises and hand clapping movements. In the second stage, deep breathing exercises will be performed. After the deep breathing exercises, in the third stage, childlike games will be used to help induce laughter. In the final stage, laughter exercises will be conducted. Laughter yoga sessions will be conducted twice a week for 8 weeks, for a total of 16 sessions. Each session will be 30 minutes in duration.
Control group
NO INTERVENTIONParticipants in this group will consist of people who do not routinely do any practice on their own to reduce stress and burnout levels. The researcher will ask the participants via phone 4 times a week for 1 month whether they have taken any action to reduce their stress and burnout symptoms. Participants who use any of the pharmacological or non-pharmacological practices to reduce stress and burnout symptoms will be excluded from the study.
Interventions
Part 1: Deep Breathing Exercises: Raise the arms up towards the sky and take a deep breath as possible and hold the breath for 4-5 seconds. This application is repeated several times. This section takes approximately 5-10 minutes. Part 2: Warm-up exercises: Hands are kept parallel to each other and clapped. The tips of the fingers and palms touch each other, the acupuncture points on both hands are stimulated and the individual's energy level increases. Section 3: Childish Games: In this section there are childish games. These games are visualized in the mind and the participants are asked to raise their arms upwards in the shape of the letter "Y".This section takes approximately 10 minutes. Section 4: Laughter Exercises: Participants are given verbal guidance such as "Put your hand on your heart, feel your heartbeat, let's exhale with a smile, let's make a wish or pray" and the laughter exercise is terminated. This section takes approximately 15 minutes.
Eligibility Criteria
You may qualify if:
- Volunteering to participate in the research
- Fully answering survey and scale forms
- Ability to read and understand Turkish
- Being between the ages of 18 and 25 years
- Having regular menstruation (between 21 and 35 days)
You may not qualify if:
- Unwilling to continue working
- Having any problem that prevents communication (such as hearing, speaking, and understanding abilities),
- Having a gynecological disease (abnormal uterine bleeding, uterine fibroids, ovarian cysts, hormonal treatment, etc.)
- Having a chronic or physical illness
- Having a mental illness
- Being under psychiatric treatment (Pharmacotherapy or psychotherapy)
- Taking medication for menopausal symptoms
- Using one of the pharmacological or non-pharmacological methods to reduce premenstrual symptoms (COCs, acupressure, homeopathy, etc.)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cukurova University
Adana, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
ELIF DAGLI, Phd
Cukurova University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asssociate professor
Study Record Dates
First Submitted
July 10, 2025
First Posted
July 20, 2025
Study Start
December 25, 2025
Primary Completion
December 25, 2025
Study Completion
December 30, 2025
Last Updated
January 27, 2026
Record last verified: 2026-01