NCT05312099

Brief Summary

work completed but not yet published

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2019

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 14, 2019

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 17, 2019

Completed
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

February 16, 2021

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

December 3, 2021

Completed
4 months until next milestone

First Posted

Study publicly available on registry

April 5, 2022

Completed
Last Updated

April 5, 2022

Status Verified

March 1, 2022

Enrollment Period

3 months

First QC Date

December 3, 2021

Last Update Submit

March 28, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • The effect of menopause on sexual life and depression: a case-control study.

    Data completed in April 2019

    14.01.2019-16.02.2021

Study Arms (2)

Case group

Women who have entered early menopause (before the age of 40), have chronic systemic diseases (diabetes, heart disease, hypertension, thyroid, rheumatic disease, psychiatric disease history), and use psychiatric drugs were not included in the study.

Other: Case control

Control group

Women under the age of 45, over the age of 55 with chronic systemic diseases (diabetes, heart disease, hypertension, thyroid, rheumatic disease, psychiatric disease history) and using psychiatric drugs were not included in the study.

Other: Case control

Interventions

Case control study

Case groupControl group

Eligibility Criteria

Age45 Years - 65 Years
Sexfemale
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Çorum Hitit University Erol Olçok Training and Research Hospital Obstetrics and Gynecology Policlinic was composed of 200 married women between the ages of 45-65, 113 of them in the postmenopausal period and 87 of them did not go through menopause.

You may qualify if:

  • Case group: Women between the ages of 45-65, who are in the postmenopausal period, who are literate, who do not have communication difficulties / mental disabilities, and who volunteer to participate in the study were included.
  • Control Group: Women between the ages of 45-55, who were not menopausal, who were literate, who had no communication difficulties / mental disabilities and who volunteered to participate in the study were included.

You may not qualify if:

  • For case group: Women with premature menopause (before the age of 40), chronic systemic disease (diabetes, heart disease, hypertension, thyroid, rheumatic disease, psychiatric disease history) and using psychiatric drugs were not included in the study.
  • For control group: Women under the age of 45, over the age of 55 with chronic systemic diseases (diabetes, heart disease, hypertension, thyroid, rheumatic disease, psychiatric disease history) and using psychiatric drugs were not included in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hitit university

Çorum, Turkey (Türkiye)

Location

MeSH Terms

Conditions

DepressionSexual Dysfunction, Physiological

Interventions

Case-Control Studies

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorGenital DiseasesUrogenital Diseases

Intervention Hierarchy (Ancestors)

Epidemiologic StudiesEpidemiologic Study CharacteristicsEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Fatma Yıldırım

    Fatma

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research assistant

Study Record Dates

First Submitted

December 3, 2021

First Posted

April 5, 2022

Study Start

January 14, 2019

Primary Completion

April 17, 2019

Study Completion

February 16, 2021

Last Updated

April 5, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will not share

Locations