Evaluation of Covid 19 Anxiety in Endometriosis Patients
Endometriosis Patients Covid 19 Anxiety
1 other identifier
observational
80
1 country
1
Brief Summary
It is aimed to measure the general anxiety and lifestyle information of endometriosis patients about covid 19 pandemic, to evaluate anxiety levels in this period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2020
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 5, 2020
CompletedStudy Start
First participant enrolled
April 5, 2020
CompletedFirst Posted
Study publicly available on registry
April 7, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
April 25, 2020
CompletedMay 20, 2020
May 1, 2020
15 days
April 5, 2020
May 18, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Covid 19 Anxiety levels in Endometriosis Patients
The Beck Anxiety Inventory (BAI); it measures the frequency of anxiety symptoms experienced by the patient. It consists of 21 questions in total. Each item gets an increasing score between 0-3. The total score ranges from 0 - 63. The following guidelines are recommended for the interpretation of scores: 0 -9, normal or no anxiety; 10 -18, mild to moderate anxiety; 19 -29, moderate to severe anxiety; and 30 - 63, severe anxiety.
20 days
Eligibility Criteria
Evaluation of endometriosis patients anxiety and lifestyle during the covid 19 pandemic
You may qualify if:
- endometriosis patients
- no psychiatric illness
- no antidepressant use
You may not qualify if:
- women who had not endometriosis
- no extra health conditions
- women younger than 18 and older than 45
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pinar Yalcin Bahat
Istanbul, İ̇stanbul, 34000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 20 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 5, 2020
First Posted
April 7, 2020
Study Start
April 5, 2020
Primary Completion
April 20, 2020
Study Completion
April 25, 2020
Last Updated
May 20, 2020
Record last verified: 2020-05