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Completed

NCT Number: NCT04009902

Evaluation of Depression and Sleep Disorders in Endometriosis Patients

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.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Kanuni Sultan Süleyman Training and Research Hospital, Istanbul, Turkey (Türkiye)

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Beck Depression Scale and Pittsburgh Sleep Quality Index

Behavioral

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

Primary outcomes

  1. Beck Depression Scale

    Time frame: 1 week

    postoperative depression in endometriosis patients will be evaluated. Consists of 21 questions scored between 0-3.

    HIGH SCORE SHOWS TO HIGH DEPRESSION. (0-63 POINTS)

  2. Pittsburgh Sleep Quality Index

    Time frame: 1 week

    postoperative sleep disorders of endometriosis patients will be evaluated. Consists of 9 questions scored between 0-3.

    HIGH SCORE SHOWS BAD SLEEP QUALITY. (0-27 POINTS)

Sponsors and collaborators

Lead sponsor

Kanuni Sultan Suleyman Training and Research Hospital

Other

Registry information

Official study title

Evaluation of Depression and Sleep Disorders in Endometriosis Patients Preoperatively and Postoperatively

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jul 5, 2019
Registry last updated
May 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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