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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05644613
Other study ID # 2
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 15, 2022
Est. completion date April 30, 2023

Study information

Verified date January 2023
Source Badr University
Contact MARIAM Dr EL EBRASHY, Phd
Phone 01001716570
Email Mariam.elabrashi@buc.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Many girls experience premenstrual syndrome PMS which is re a group of physical, cognitive, affective, and behavioural symptoms that occur cyclically during the luteal phase of the menstrual cycle and resolve at or within a few days of the onset of menstruation. In young adolescents symptoms might particularly affect school functions, and social interactions in a negative ways in this study we will figure out the effect of 2 kinds of exercises in the management of this syndrome.


Description:

Fourty adolescent girls were divided randomly into two equal groups, Group (A) will consist of (20) adolescent girls age ranged from 14-17 suffering from PMS without any pathological cause they will receive an aerobic exercise on land in form of walking on the treadmill for 20 min 3 times per week for 3 months. Group (B) will consist of (20) adolescent girls age ranged from 14-17 suffering from PMS without any pathological cause they will receive an aerobic exercises in water in form of walking on the treadmill for 20 min 3 times per week for 3 months the assessment of the PMS symptoms will be done by Premenstrual distress questionnaire


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date April 30, 2023
Est. primary completion date March 2, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 14 Years to 17 Years
Eligibility Inclusion Criteria: - All participants virgin females. - Their age ranged from 14 to 17 years old - their body mass index (BMI) = 18 = 25 kg/m2. - They are clinically and medically stable during the study, - they have regular menstrual cycle of 23 to 35 days and not participated any type of unusual diet during the period of the study. Exclusion Criteria: - All females in this study are free from: cardiopulmonary or orthopaedic problems, taking any hormonal drugs for three months at least, participating in any form of activity rather than the prescribed one in the study, any abnormality in ovulation or pelvic inflammatory diseases (PID).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
aerobic exercise on land
aerobic exercise on land in form of walking on the treadmill
aerobic exercise in water
aerobic exercises in water in form of walking on the treadmill

Locations

Country Name City State
Egypt Badr University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Mariam Hossam El Ebrashy

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Premenstrual syndrome symptoms PREMENSTRUAL SYNDROME QUESTIONNAIRE 3 months
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