Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
105 participants
OBSERVATIONAL
2024-01-01
2025-05-30
Brief Summary
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Detailed Description
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Data are collected through the administration of the validated Temperament Evaluation of Memphis, Pisa, Paris and San Diego Autoquestionnaire (TEMPS-A) and the Menopause Rating Scale (MRS).
Participants voluntarily complete the questionnaires after providing informed consent. All responses are anonymized and securely stored.
Quality assurance measures include verification of data entry, use of validated scales, and compliance with ethical standards approved by the Istanbul Medipol University Non-Interventional Clinical Research Ethics Committee.
No interventions are applied; the study strictly follows observational registry procedures.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* Ability to complete questionnaires and provide informed consent
Exclusion Criteria
* History of surgical menopause (bilateral oophorectomy)
* Presence of severe physical disorders (e.g., malignancy, severe cardiovascular diseases)
* Presence of severe psychological disorders (e.g., major depressive disorder, psychosis)
55 Years
FEMALE
Yes
Sponsors
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Bagcilar Training and Research Hospital
OTHER_GOV
Responsible Party
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Cemile ilhan
Principal Investigator, Obstetrics and Gynecology Specialist
Principal Investigators
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Cemile Ilhan, MD
Role: PRINCIPAL_INVESTIGATOR
Bagcilar Training and Research Hospital
Locations
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Bağcılar Training and Reserach Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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777/28.09.23
Identifier Type: -
Identifier Source: org_study_id
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