Primary Dysmenorrhea Severity in Athletic vs. Non-Athletic Females

Sponsor
Cairo University (Other)
Overall Status
Completed
CT.gov ID
NCT06075654
Collaborator
(none)
628
1
7.1
88.5

Study Details

Study Description

Brief Summary

The aim of the study is to investigate the difference in the severity of primary dysmenorrhea between athletic and non-athletic females.

Condition or Disease Intervention/Treatment Phase
  • Other: no intervention it is considered (Epidemiological Study)

Detailed Description

Primary dysmenorrhea is defined as colic pain in the lower abdomen which starts with the onset of menstruation. It is one of the most common gynecological disorders, an important cause of morbidity, and the most common cause of pelvic pain in menstruating girls and women it affects women in any age group. The prevalence varies widely, ranging from 17% to as high as 91%. Between 16% to 29% of women with dysmenorrhea have significant impairment in quality of life and the women's well-being. The rate of absenteeism from school, work, or other activities represents up to 15% of women with dysmenorrhea, dysmenorrhea is considered a source of considerable economic losses due to the costs of medications, medical care, and decreased productivity. Yoga, pilates, stretching, and other types of exercises have a noticeable effect on decreasing pain, and improving general health, and quality of sleep with different health conditions including primary dysmenorrhea. In addition, exercise and physical activity are used widely and proven to not only decrease pain but also improve quality of life, decrease stress, improve mental health, and in management of depression and stress.

For dysmenorrhea the mechanism that explained the effect of exercises on primary dysmenorrhea has been classified according to the intensity of the exercises; moderate -high-intensity exercise was believed to increase the anti-inflammatory cytokines, decrease the overall amount of prostaglandins released because of the decrease of the overall amount of menstrual flow. Low-intensity exercise reduces cortisol levels and prostaglandin synthesis

Study Design

Study Type:
Observational
Actual Enrollment :
628 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
"Comparison of the Severity of Primary Dysmenorrhea Between Athletic and Non-Athletic Females: A Cross-Sectional Study" Comparison of the Severity of Primary Dysmenorrhea Between Athletic and Non-Athletic Females: A Cross-Sectional Study.
Actual Study Start Date :
Mar 1, 2023
Actual Primary Completion Date :
Sep 21, 2023
Actual Study Completion Date :
Oct 3, 2023

Arms and Interventions

Arm Intervention/Treatment
Athletic Group

athletic females complaining of primary dysmenorrhea, they participated in the exercise for the last ≥ 6 months, did exercises for ≥ 3 days/ week, and practiced (swimming, basketball, volleyball, gymnastics, judo, wrestling, karate, and boxing.

Other: no intervention it is considered (Epidemiological Study)
It was a survey used Visual Analog Scale and WaLIDD scale to measure the severity of primary dysmenorrhea between both groups

Non-Athletic Group

Non-athletic females complaining form primary dysmenorrhea who are have not participated in any physical activity before

Other: no intervention it is considered (Epidemiological Study)
It was a survey used Visual Analog Scale and WaLIDD scale to measure the severity of primary dysmenorrhea between both groups

Outcome Measures

Primary Outcome Measures

  1. Visual Analogue Scale [Data will be collected at a single time point, which is the baseline assessment]

    The scale that will be used the VAS ;each subject will instructed to put point on line from no pain to tolerable pain

Secondary Outcome Measures

  1. Working ability, location, Intensity, Disability Dysmenorrhea scale. [Data will be collected at a single time point, which is the baseline assessment]

    measuring a combination of manifestations: subjective (intensity /Wong-Baker, work ability) and objective (days of pain, location). In which each aspect of scale are rated from 0 to 3. 0 indicate no dysmenorrhea, 1-4 mild dysmenorrhea, 5-7 moderate dysmenorrhea, 8-12 sever dysmenorrhea.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 28 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Common inclusion criteria for athletic and non-athletic female.
  1. They had a regular menstrual cycle with a menstrual cycle length of 21-30 days.

  2. All females were virgins.

  3. Their ages ranged from 18 to 28 years old.

  4. Their BMI was ranged from 18.5 -29,9 kg/m2

  5. They did not use any pharmacological therapies for controlling pain during menstruation and during the application of the study.

Inclusion criteria athletic female:
  1. They participated in the exercise for the last ≥ 6 months.

  2. They did exercises for ≥ 3 days/ week.

  3. They practiced (swimming, basketball, volleyball, ballet, gymnastics, judo, wrestling, karate, and boxing).

Exclusion Criteria:
  1. History of pelvic pathology or any gynecological disease.

  2. They had a history of chronic illness (eg: diabetes).

  3. Their symptoms of dysmenorrhea became worse over time

Contacts and Locations

Locations

Site City State Country Postal Code
1 Khloud Ramadan Abd El- Fatah Cairo Egypt

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
khloud ramadan Abd El- fatah, principle investigator, Cairo University
ClinicalTrials.gov Identifier:
NCT06075654
Other Study ID Numbers:
  • P.T.REC/012/004091
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 16, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 16, 2023