Back to resultsCounseling of Pregnant Women During Corona
Primary Purpose
Respiratory Tract Infections
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Women receiving extra remembering by healthcare
Sponsored by
About this trial
This is an interventional supportive care trial for Respiratory Tract Infections
Eligibility Criteria
Inclusion Criteria:
- pregnant women
Exclusion Criteria:
- non pregnant women
Sites / Locations
- Algazeerah and Kasralainy hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
patients receiving remembering
patients not receiving extra remembering
Arm Description
Outcomes
Primary Outcome Measures
The number of pregnant women who know the exact symptoms of the disease
The number of pregnant women who have awareness about the disease
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04317365
Brief Title
Counseling of Pregnant Women During Corona
Official Title
Effect of Counseling Between Pregnant Women During Corona Infection
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
March 24, 2020 (Actual)
Primary Completion Date
April 26, 2020 (Actual)
Study Completion Date
May 25, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Aljazeera Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Corona virus is known as covid 19 And is transmitted through droplet infection
Detailed Description
Symptoms of Corona include cough Fever and dyspnea
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Tract Infections
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
patients receiving remembering
Arm Type
Active Comparator
Arm Title
patients not receiving extra remembering
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Women receiving extra remembering by healthcare
Intervention Description
Women receiving extra remembering by healthcare in covid infection
Primary Outcome Measure Information:
Title
The number of pregnant women who know the exact symptoms of the disease
Description
The number of pregnant women who have awareness about the disease
Time Frame
Within one month
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant women
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
43 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
pregnant women
Exclusion Criteria:
non pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mahmoud Alalfy
Organizational Affiliation
Algezeera hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Algazeerah and Kasralainy hospital
City
Giza
Country
Egypt
12. IPD Sharing Statement
Learn more about this trial
Counseling of Pregnant Women During Corona
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