Sexual Functions and Marital Adjustment for Spouses in Menopause

NCT ID: NCT05338645

Last Updated: 2022-04-21

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

127 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-09-14

Study Completion Date

2019-05-18

Brief Summary

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Objective: This study was conducted as a cross-sectional descriptive study in order to determine the effect of menopause on the SFs and marital adjustment of the spouses.

Detailed Description

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Objective: This study was conducted as a cross-sectional descriptive study in order to determine the effect of menopause on the SFs and marital adjustment of the spouses.

Materials and Methods: The sample of the study consisted of a total of 254 people, 127 of whom were postmenopausal women and their spouses. The data were collected with The Descriptive Information Form (DIF), The Female Sexual Function Scale (FSFS) and the Arizona Sexual Experiences Scale (ASES), The Marital Adjustment Scale (MAS). T test was used for two-group comparison of parametric data, Mann Whitney U test was used for two-group comparison of non-parametric data, and Kruskal Wallis Test was used for non-parametric data comparison of more than two groups. In addition, the relationship between the mean scores of FSFS, ASES and MAS was evaluated with Spearman's rho Correlation analysis.

Conditions

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Menopause

Study Design

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Observational Model Type

FAMILY_BASED

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* The sample of the study consisted of women aged between 45-65,
* who were aged between 45-65,
* had at least 1 year of menopause,
* had no communication barriers,
* volunteered to participate in the research, -lived in the same house with their spouses, -
* had sexual activity in the last four weeks,
* selected using the simple random sampling method.

Exclusion Criteria

* have diabetes,
* have hypertension,
* have depression
Minimum Eligible Age

45 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hitit University

OTHER

Sponsor Role lead

Responsible Party

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Fatma Yildirim

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fatma Yıldırım

Role: PRINCIPAL_INVESTIGATOR

Hitit University

Locations

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Fatma Yıldırım

Çorum, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2017-38

Identifier Type: -

Identifier Source: org_study_id

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