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Premenstrual Syndrome clinical trials

View clinical trials related to Premenstrual Syndrome.

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NCT ID: NCT05834127 Completed - Pain Clinical Trials

Effects of Aerobic Exercises and Yoga on Premenstrual Syndrome

Start date: November 20, 2022
Phase: N/A
Study type: Interventional

Sign and symptoms including mood swings, sensitive breasts, food cravings, exhaustion, irritability, pain and sadness. The physical and emotional changes you go through with premenstrual syndrome can range from hardly perceptible to severe. Some people's physical discomfort and emotional stress are so severe that it interferes with their daily life. Regardless of the severity of the symptoms, most women's signs and symptoms go away four days following the start of their menstrual cycle. In this study the effects of aerobic exercises and Yoga on premenstrual syndrome population will be analyzed. This study will be a randomized clinical trial which will incorporate two different interventions. Aerobic exercises and yoga would be administered to the females. 32 patients will randomly divided into two groups. Assessment will be done by using PMS scale and visual analogue scale. The goal of this study to compare the effects of aerobic exercises and yoga on premenstrual syndrome.

NCT ID: NCT05811130 Completed - Clinical trials for Premenstrual Syndrome

Premenstrual Syndrome and Its Influencing Factors Such as Physical Activity, Perceived Stress and Mental Status

Start date: June 1, 2021
Phase:
Study type: Observational

Our research aimed to investigate how a sedentary lifestyle, body mass index, depression, and stress affect the severity of PMS symptoms and how the listed factors influence each other.

NCT ID: NCT05725447 Completed - Clinical trials for Premenstrual Syndrome

Cross-cultural Adaptation, Validity and Reliability of the Turkish Version of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ)

Start date: November 7, 2022
Phase:
Study type: Observational

This study is aimed to carry out the Turkish version validity and reliability of the Premenstrual Syndrome Impact Questionnaire (PMS-IQ).

NCT ID: NCT05709561 Completed - Clinical trials for Premenstrual Syndrome

The Effect of Acupressure and Mindfulness to Cope With Premenstrual Syndrome (PMS) on PMS and Quality of Life

Start date: March 31, 2022
Phase: N/A
Study type: Interventional

The research was carried out to determine the effect of acupressure and mindfulness practice to cope with premenstrual syndrome on premenstrual symptoms and quality of life. The sample of the study consisted of a total of 270 students, 90 of which were acupressure, 90 mindfulness and 90 control groups. In the study, data were collected with the Participant Information Form, PMSS and WHOQOL-BREF. The acupressure group was asked to apply acupressure two days a week for 12 weeks, a total of 24 times. In the mindfulness group, 8 weeks of Conscious Awareness Stress Reduction Program was applied, after which the students were asked to practice mindfulness for 3 cycles. Students in both experimental groups were asked to stop the practices after acupressure and mindfulness practices. PMSS and WHOQOL-BREF were applied to both experimental and control groups as an intermediate test 12 weeks after the pre-test and a post-test 24 weeks later.

NCT ID: NCT05707845 Completed - Clinical trials for Premenstrual Syndrome

Effect of Weight Reduction and Aerobic Exercise on PMS Symptoms in Obese Females

PMS
Start date: May 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this study will be investigation of the effect of weight reduction and aerobic exercises on premenstrual syndrome symptoms in obese females.

NCT ID: NCT05697536 Completed - Clinical trials for Premenstrual Syndrome

Comparison of Pilates and Aerobic Exercises on Pain, Anxiety and QOL in PMS

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

The significance of this study is that it may improve the premenstrual symptoms like pain and anxiety in females with premenstrual syndrome and improve their quality of life. This study may add to the growing body of knowledge that if these two techniques yield comparable outcomes and if one technique is superior to the other, which should be the alternative choice of therapy. Therefore, the study will be done to compare the effects of Pilate exercises and aerobic exercises on pain, anxiety and quality of life in females with premenstrual syndrome.

NCT ID: NCT05692479 Completed - Clinical trials for Premenstrual Syndrome

Premenstrual Syndrome and Physical Activity Self-Worth

Start date: October 10, 2022
Phase:
Study type: Observational [Patient Registry]

Premenstrual syndrome (PMS) negatively affects the quality of life of millions of women. PMS is a common cyclic disorder characterized by somatic, cognitive, emotional and behavioral symptoms that usually occurs in young and middle-aged women, lasts during the luteal phase of the menstrual cycle and ends with the onset of menstruation.Studies have shown that women with high PMS symptoms are more inactive. Physical activity participation in women affects a wide spectrum of self-perceptions, including knowledge, social, and emotional self-perceptions. By determining which physical, emotional, social and academic/knowledge areas are affected by women, increasing their participation in physical activity can be achieved. The subject of the study is to determine the symptom severity of women with and without premenstrual syndrome and to examine how premenstrual syndrome affects physical activity self-worth.

NCT ID: NCT05556252 Completed - Clinical trials for Premenstrual Syndrome

The Effect of Hydrogen-rich Water on Premenstrual Symptoms and Quality of Life

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of hydrogenated water on premenstrual symptoms and quality of life in students with premenstrual syndrome. Research Hypotheses H1 1 Hydrogenated water consumption reduces premenstrual symptoms in students with premenstrual syndrome. H1 2 Hydrogenated water consumption increases the quality of life in students with premenstrual syndrome. The research will consist of intervention and control groups. Individuals consuming hydrogen-rich water will be included in the intervention group, whereas individuals consuming normal water will be in the control group. The block randomization method will be used to randomly assign participants who meet the research criteria to the groups. Participants will be provided with hydrogenated water for three cycles.

NCT ID: NCT05507255 Completed - Clinical trials for Premenstrual Syndrome

Effect of Aerobic Exercise on Diurnal Cortisol Pattern in Premenstrual Syndrome

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

The aim of this study will be to investigate the effect of aerobic exercise on diurnal cortisol pattern in premenstrual syndrome.

NCT ID: NCT05499000 Completed - Clinical trials for Premenstrual Syndrome

The Effect of Emotional Freedom Technique on Premenstrual Syndrome

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

Objective: This study was conducted to evaluate the Effect of Emotional Freedom Technique on Premenstrual Syndrome. Methodology: The research will be conducted as a randomized controlled trial. The research will be carried out with students studying at the Department of Midwifery, Faculty of Health Sciences, İnönü University, between September and October 2022. The sample size of the study was calculated as 102 people with an effect size of 0.80 and a power of 0.95. Premenstrual syndrome scale will be applied to all students participating in the research first and those who score 110 and above will be listed. Experimental and control groups will be determined by randomization. Personal information form, subjective experience unit scale and premenstrual syndrome scale will be used to collect data. SPSS 22.0 package program will be used in the evaluation of the data. The independent variable of the research is the emotional liberation technique. The dependent variable of the study is the mean scores of the participants from the subjective experience unit scale and premenstrual syndrome scale.