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Premenstrual Syndrome clinical trials

View clinical trials related to Premenstrual Syndrome.

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NCT ID: NCT05395156 Not yet recruiting - Premenstrual Pain Clinical Trials

EFFECT OF TENS ON ACUPOINTS IN PREMENSTRUAL SYNDROME

Start date: June 10, 2022
Phase: N/A
Study type: Interventional

These will be no effect of transcutaneous electrical acupoint stimulation on premenstrual syndrome Does transcutaneous electrical acupoint stimulation affect premenstrual syndrome (PMS)?

NCT ID: NCT05349344 Completed - Quality of Life Clinical Trials

Effect of Aerobic Exercise on Premenstrual Syndrome Symptoms (PMS).

PMS
Start date: September 20, 2020
Phase: N/A
Study type: Interventional

To Determine the Effect of Regular Aerobic Exercise Training on Severity of Premenstrual Syndrome Symptoms and Health-Related Quality of life on working women.Exercise can be used as an alternative therapy in reducing premenstrual symptoms.But still there is lack of Literature on PMS in work Place and effect of Treatments to improve overall Quality of life in working women.And this study aims to fill the gap by assessing the impact that Premenstrual Syndrome can have on working women's Quality of life and can be used to establish a model of regular exercise program with the potential to decrease premenstrual symptoms and improve quality of life for a menstrual health-friendly workplace environment for Female Employees.

NCT ID: NCT05340816 Enrolling by invitation - Clinical trials for Premenstrual Syndrome

The Effects of Manual Lymphatic Drainage and Transcutaneous Electrical Nerve Stimulation in Premenstrual Syndrome

Start date: April 4, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to (a) investigate the effects of manual lymphatic drainage and transcutaneous electrical nerve stimulation on the severity of syndrome symptoms, pain, heart rate variability, and quality of life in women with premenstrual syndrome, and (b) compare the effectiveness of these two methods. Female participants who met the inclusion criteria and volunteered to participate in the study will be called approximately one week before menstruation. After the participants are randomly divided into 3 groups, their baseline assessments will be made. Then, the participants will be treated according to the group they are assigned to. Treatments will be applied for 5 days and once a day. No treatment will be applied to the control group. The assessments will be repeated after the treatment, on 1st day of menstruation, two days before the next menstruation, and on the first day of the next menstruation. The hypothesis of this study is that manual lymphatic drainage and transcutaneous electrical nerve stimulation have positive effects on the severity of premenstrual syndrome symptoms, pain, heart rate variability, and quality of life.

NCT ID: NCT05290181 Completed - Clinical trials for Premenstrual Syndrome

The Effect of Pilates Exercise and Whatsapp Text-Based Support Program on Premenstrual Syndrome (PMS) Symptoms

PMS
Start date: January 12, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of Pilates exercise and Whatsapp text message-based support program on PMS symptoms experienced by university female students.

NCT ID: NCT05264519 Recruiting - Clinical trials for Premenstrual Syndrome

The Effect of Foot Bath on PMS, Sleep and Quality of Life Among University Students With PMS

Start date: November 6, 2021
Phase: N/A
Study type: Interventional

Premenstrual syndrome is a cyclical disorder characterized by physical and emotional symptoms that appear in the late luteal phase of the menstrual cycle and subside within a few days with the onset of menstruation. Non-pharmacological methods should be recommended first to women who experience PMS symptoms. For this purpose, it is planned to apply foot bath to university students with premenstrual syndrome. The study was planned as a randomized controlled single-blind study. The universe of the research will be female students studying at Ordu University Faculty of Education in the 2021-2022 academic year. In the first stage of the study, female students who are 18 years of age and older and who voluntarily agree to participate in the research will be taken without making a sample selection. Considering the possibility of data loss during the research process, it was planned to work on 39 intervention and 39 control groups, including a total of 78 women In the collection of data; Personal Information Form, Premenstrual Syndrome Scale (PMSS), Pittsburgh Sleep Quality Index (PSQI), SF-36 Quality of Life Scale will be used. PSQI and SF-36 Quality of Life Scale will be applied to students in the intervention group. The foot bath will be applied for 3 months, starting 7-10 days before the menstrual cycle, that is, in the luteal phase of the menstrual cycle. Students will be asked to fill out the Footbath Monitoring Form in order to assess whether they have taken a footbath. Those who apply foot bath at least 7 times will be included in the study. In case of less than seven students, the student will be excluded from the research and the new student who meets the criteria will be included in the research. At the end of each cycle, PMSÖ, PSQI and SF-36 will be administered to the students by the researcher. When the students in the Control Group are determined, PSQI and SF-36 will be applied by the researcher, and then PMSÖ, PSQI and SF-36 will be applied at the end of each cycle.

NCT ID: NCT05237661 Completed - Menstrual Pain Clinical Trials

Study to Evaluate Your Super's Moon Balance and Its Impact on Premenstrual Syndrome

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

This is an open-label observational single-group clinical trial to study the efficacy of a commercially available dietary supplement and its effect on common PMS and menstrual symptoms, as well as health-related biomarkers.

NCT ID: NCT05198115 Not yet recruiting - Clinical trials for Premenstrual Syndrome

Premenstrual Syndrome in Young Women With Eight Weeks of Aerobic Exercise

Start date: February 25, 2022
Phase: N/A
Study type: Interventional

The premenstrual syndrome includes physical and psychological symptoms that occur at the end menstrual cycle and exercise is one of the ways to reduce symptoms. The aim of this study was to determine the effect of a regular 8-week aerobic exercise program on psychological symptoms of premenstrual syndrome.

NCT ID: NCT05191108 Completed - Clinical trials for Premenstrual Syndrome

Premenstrual Syndrome (PMS) and Mindfulness Stress Reduction Program (MSRP)

PMS and MSRP
Start date: February 21, 2022
Phase: N/A
Study type: Interventional

Premenstrual syndrome (PMS) is a disorder characterized by emotional, physical and behavioral symptoms that increase the severity of the menstrual cycle in women of reproductive age during the luteal phase and disappear spontaneously a few days after the onset of menstruation. Nonpharmacological applications are often preferred to reduce premenstrual symptoms. It has been stated that with the meditation practices of mindfulness, individuals experience less anxiety, depression, anger and lower levels of psychological distress, including anxiety. . It is thought that the mindfulness stress reduction program can reduce the symptoms of PMS by regulating the stress level and emotional balance of women.

NCT ID: NCT05144568 Completed - Clinical trials for Premenstrual Syndrome

The Effect of Nutrition Education on Premenstrual Syndrome

Start date: June 3, 2019
Phase: N/A
Study type: Interventional

The aim of our study is to examine the effect of nutritional education given to university students with premenstrual syndrome (PMS) on premenstrual symptom severity, nutrient intake and anthropometric measures. Our hypothesis is that nutrition education reduces symptoms in students with PMS. The effect of nutrition education on premenstrual syndrome was evaluated. The sample for this study included 83 female students, with 43 in the experimental and 40 in the control group, who were studying at the health sciences faculty of a state university and met the inclusion criteria. Experimental and control groups were formed by randomized method. Nutrition training was given to the experimental group. Participant data were collected before and four months after nutrition training. The data were collected with the personal information form, Premenstrual Syndrome Scale and food consumption record form. Nutrient amounts were determined in the Nutrition Information System (BEBÄ°S) program.

NCT ID: NCT04955912 Completed - Clinical trials for Premenstrual Syndrome

Music and Premenstrual Symptoms and Quality of Life

Start date: January 30, 2021
Phase: N/A
Study type: Interventional

Premenstrual syndrome is an important health problem affecting women of childbearing age. This study is a prospective, single-blinded randomized controlled trial. Participants were randomized into music, and control groups. Immediately post-intervention, the women in the experimental groups had significantly higher reduce premenstraul syndrome levels and increase a quality life.