Evaluation of Depression and Sleep Disorders in Endometriosis Patients

NCT ID: NCT04009902

Last Updated: 2020-05-22

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

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-07-03

Study Completion Date

2020-05-03

Brief Summary

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The aim of this study was to compare the depression and sleep disturbances of operated endometriosis patients before and after the operation. The main objective here is to provide data on how patients' psychological states and sleep patterns are affected by the symptoms of endometriosis and how these effects can be corrected. In this way, it is aimed to determine whether the patients have psychological support needs and to give the planned treatment due to endometriosis in the early period. As a secondary goal, it is planned to keep the patients in follow-up with their improved sleep and psychological conditions, and to improve their adherence to treatment and quality of life.

Detailed Description

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Conditions

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Endometriosis Sleep Depression

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Beck Depression Scale and Pittsburgh Sleep Quality Index

postoperative depression and sleep disorders in patients with endometriosis will be evaluated

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 18-49 years of age with no known psychiatric disorder and
* Endometriosis patients with indications for operation

Exclusion Criteria

* Patients receiving only medical treatment without any indication for operation,
* those with a known psychiatric disease,
* patients with sleep disorders due to another reason,
* Patients over the age of 49, patients under the age of 18,
* Patients with malignancy,
* pregnant women
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Kanuni Sultan Suleyman Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Pınar Kadirogulları

Principal investigator, M.D, Department of Obstetrics and Gynecology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kanuni Sultan Süleyman Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Pınar Kadiroğulları

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2019.03.77

Identifier Type: -

Identifier Source: org_study_id

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