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NCT05198115 Clinical Trial

Premenstrual Syndrome in Young Women With Eight Weeks of Aerobic Exercise

Premenstrual Syndrome Clinical Trial

Official title:
Premenstrual Syndrome in Young Women With Eight Weeks of Aerobic Exercise

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05198115
Other study ID # 3574
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 25, 2022
Est. completion date April 30, 2022

Study information
Verified date February 2022
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Description:

Premenstrual syndrome is characterized by the presence of both physical and behavioral (including affective) symptoms that occur repetitively in the second half of the menstrual cycle and interfere with some aspects of the woman's life(1). The core symptoms of PMS include affective symptoms, such as irritability, depression, anxiety, and somatic symptoms, such as breast pain, bloating, swelling, and headache (2). Women with moderate to severe PMS symptoms had a reduction in health-related quality of life(3) and work productivity, increased work absenteeism, and visits to ambulatory healthcare providers (4), so the treatment of this syndrome is essential.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date April 30, 2022
Est. primary completion date April 25, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - young women aged 18-25 years with a body mass index (BMI): 18-25 kg/m2, having regular menstrual cycles of 23-35 days duration, no previous practice of aerobic exercise, free from musculoskeletal injury, not using oral contraceptive pills or taking any psychotropic agents, having no depression or genital tract diseases Exclusion Criteria: - pregnancy, contraindications to physical exercise, metabolic or cardiorespiratory illness, cigarette smokers, women who recover from a major injury or using anti-inflammatory, hyperlipidemia or hypertension medications, any abnormality in ovulation, and women with diabetes mellitus, thyroid, pituitary, or ovarian disorders

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• aerobic exercise
aerobic training for 8 weeks, 3 times a week, and 60 min each time

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Al-Azhar University

Outcome
Type Measure Description Time frame Safety issue
Primary Emotional (EM) scale emotional scale from [0 to 10] eight weeks
See also
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