Investigating temperament traits and menopause symptoms in women
The Relationship Between Temperament and Menopause Symptoms: A Cross-Sectional Study Using TEMPS-A and MRS Scales
This study looks at how different personality traits might affect the symptoms women experience during menopause.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | N/A to 55 Years |
| Sex | Female |
| Sponsor | Bagcilar Training and Research Hospital Government |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06972290 on ClinicalTrials.gov |
What this trial studies
This observational study examines the relationship between temperament traits and menopausal symptoms in women undergoing the menopausal transition. Participants are recruited from menopause outpatient clinics and complete validated questionnaires, including the TEMPS-A and Menopause Rating Scale (MRS). The study focuses on women classified in specific STRAW stages of menopause and adheres to ethical standards for data collection and storage. No interventions are applied, and the study strictly follows observational procedures.
Who should consider this trial
Good fit: Ideal candidates are women in the menopausal transition classified as STRAW stages -1, +1a, and +1b who can complete questionnaires.
Not a fit: Patients who have undergone hormone therapy in the past 6 months or have severe physical or psychological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of how personality traits influence menopausal symptoms, potentially leading to better management strategies.
How similar studies have performed: While studies on menopause symptoms exist, the specific focus on temperament traits in this context is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women classified as STRAW stages -1, +1a, and +1b (menopausal transition stages) * Ability to complete questionnaires and provide informed consent Exclusion Criteria: * History of hormone therapy during the past 6 months * 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)
Where this trial is running
Istanbul
- Bağcılar Training and Reserach Hospital — Istanbul, Turkey (Recruiting)
Study contacts
- Principal investigator: Cemile Ilhan, MD — Bagcilar Training and Research Hospital
- Study coordinator: Cemile Ilhan, MD
- Email: drcemileilhan@gmail.com
- Phone: +90 535 891 03 05
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.