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Clinical Trials in Turkey / NCT07376408
Starting soon Observational

Spousal Support and Sexual Quality of Life in Postmenopausal Women

NCT07376408 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02
Last updated
2026-02-03

Condition(s) studied

PostmenopausalSupportSexuality

Investigational drug(s) / intervention(s)

No Intervention

No Intervention: This is an observational study. No intervention, treatment, or behavioral modification is applied. Data are collected using self-reported questionnaires only.

Study summary

Menopause is a natural transition period in women's lives characterized by concurrent hormonal, psychological, and relational changes. During the postmenopausal period, hormonal alterations are not limited to physical symptoms but also have significant effects on psychological well-being, interpersonal relationships, and particularly sexual quality of life. Common concerns during this period include decreased sexual desire, vaginal dryness, pelvic discomfort, and reduced sexual satisfaction, all of which may negatively affect overall quality of life. Sexual quality of life is influenced not only by biological factors but also by psychological and relational dimensions.

The quality of partner relationships and perceived partner support play an important role in women's adaptation to sexual changes during the postmenopausal period. However, partner support during menopause is often reported to be insufficient, which may adversely affect sexual well-being. Despite this, evidence examining the relationship between perceived partner support and sexual quality of life in postmenopausal women remains limited.

The aim of this study is to examine the effect of perceived partner support on sexual quality of life in postmenopausal women. Through this investigation, the explanatory role of partner support in postmenopausal sexual well-being is aimed.

Eligibility

Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Postmenopausal status, defined as at least 12 consecutive months of amenorrhea * Having a partner * Voluntary agreement to participate in the study and provision of written informed consent Exclusion Criteria: * Visual, cognitive, or other impairments that prevent completion of the study questionnaires * History of major gynecological surgery within the past 6 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Provincial Directorate of Health - Family Health Centers Istanbul Turkey (Türkiye)

More Istanbul University - Cerrahpasa trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07376408 on ClinicalTrials.gov ↗ ← All trials in Turkey