- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05442541
Menstrual Wellbeing in Woman Living in Turkey; an Epidemiological Study
June 30, 2022 updated by: Elif Cansu Gundogdu, Dr. Lutfi Kirdar Kartal Training and Research Hospital
Üreme çağındaki kadınlarda menstrüel Iyilik Halinin değerlendirilmesi Saha Anket çalışması/Evaluation of Menstrual Well-being in Women of Reproductive Age, Field Survey Study
Women with endometriosis in our country and around the world face various difficulties during their menstrual periods in reproductive age.
While some of these difficulties are caused by the environment, some of them are due to the insufficient development of personal consciousness.
In our study, we aim to reveal the perspective of individuals and society on the menstrual period.
Our primary aim in our study is to understand what kind of problems are experienced in different regions of our country during the menstrual period for women and how they are spent.
Secondly, the effect of this period on women's quality of life will be examined.
Study Overview
Status
Completed
Conditions
Detailed Description
Our research will be conducted between January 1, 2022, and February 1, 2022, in 7 different regions of our country, by asking questions to women of reproductive age from different groups.
Each participant will be asked to answer the survey questions and the results will be analyzed.
The survey will be done face to face.
The questionnaire contains questions about women's socio-demographic data, their perspectives on their menstrual period, their information about endometriosis, and their perspectives on pads and birth control pills.
Menstruating women of reproductive age between the ages of 18- 45 will be included in this study.
As a result of the study, the problems experienced by women of reproductive age in different regions will be evaluated.
Study Type
Observational
Enrollment (Actual)
1829
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Istanbul, Turkey
- Kartal Dr. Lutfi Kirdar Research and Training Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Menstruating women of reproductive age between the ages of 18- 45 will be included in this study.
Description
Inclusion Criteria:
- Menstruating women of reproductive age between the ages of 18- 45 will be included in this study.
Exclusion Criteria:
- Women with a history of hematological disease, cardiovascular disease, malignancy, advanced renal failure, active infection, diabetes mellitus, and pregnant women will not be included in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disparities in menstrual hygiene and well-being between 7 regions of Turkey in women of reproductive age with a questionnaire
Time Frame: 1 month
|
In this study, the effect of the menstrual period on the quality of life of 1829 women living in seven different geographical regions of our country will be examined through a questionnaire.
The goal of this study is to evaluate the menstrual well-being of women living in different regions of our country.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Ahmet Kale, Prof.Dr., Kartal Dr. Lutfi Kirdar Research and Training Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2022
Primary Completion (Actual)
February 1, 2022
Study Completion (Actual)
February 1, 2022
Study Registration Dates
First Submitted
January 12, 2022
First Submitted That Met QC Criteria
June 30, 2022
First Posted (Actual)
July 5, 2022
Study Record Updates
Last Update Posted (Actual)
July 5, 2022
Last Update Submitted That Met QC Criteria
June 30, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/514/216/15
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
not decided yet.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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