Spousal Support and Sexual Quality of Life in Postmenopausal Women

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorIstanbul University - Cerrahpasa

About this trial

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 criteria

Qualifiers

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

Disqualifiers

Visual, cognitive, or other impairments that prevent completion of the study questionnaires

History of major gynecological surgery within the past 6 months

Trial design

Treatments tested in this trial

  • No Intervention

Treatment groups

84 Participants
are divided into 1 treatment group

Sponsors and collaborators

Istanbul University - Cerrahpasa

Lead sponsor

Acibadem University

Sponsor institution