- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05968872
Assessing Knowledge & Attitude of Health Professionals Towards Anesthesia and the Anesthetist's Role.
Assessing Knowledge and Attitude of Health Professionals Towards Anesthesia and Anesthetist's Role in the Health Delivery System at Dessie Comprehensive Specialized Hospital, From May 1st to September 30th, 2022, G.C.
Study Overview
Detailed Description
Data were collected using self-administered, pretested questionnaires prepared in english and then translated into amharic. The Amharic version of the questionnaire was assessed for compatibility with the english version by a group of people who converted it back to english and compared the converted versions. The questionnaire consists of three parts. The first part was about socio-demographic characteristics; the second part was about participants' knowledge about anesthesia; and the third part was about professionals' attitudes towards anesthesia. After informing each participant about the purpose of the study and obtaining informed consent, data collection began. After the questionnaires were filled out by the participants, the two trained data collectors compiled and checked the data for any conflicts that may have occurred during the data collection.
The development and translation of the questionnaire was the most challenging task, and it was developed by both the anesthetists and anesthesiologists. The questionnaire was pre-tested on 25 randomly selected health professionals. After pre-testing, some questions were modified to make them more understandable.
Attitude-related questions were answered as strongly agree, agree, disagree, strongly disagree, and none. the investigators prepared a total of 15 knowledge-related questions, of them 10 were closed-ended and could be scored objectively.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Amhara
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Dessie, Amhara, Ethiopia, 801103
- Dessie comprehensive specilized hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All health professionals in Dessie comprehensive specialized hospital who are voluntary to participate in the study.
Exclusion Criteria:
- Group who are not voluntary,
- Anesthetists/anesthesiologists
- other institution medical staff worked as a contract at Dessie hospital
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To determine health professionals' knowledge on anesthesia service
Time Frame: from may 1 to septamber 30 2022
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The knowledge outcome was measured by dividing the correct answer to the total questions(15) as a percentage.
Percentage scores <50% are poor, 50%-75% moderate, and >75% good.
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from may 1 to septamber 30 2022
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To determine health professionals' attitude on anesthesia service
Time Frame: from may 1 to septamber 30 2022
|
The attitude was measured by the Likert scale as agree, strongly agree, disagree, strongly disagree, or none.
The likert scale is used to measure the percentage of positive or negative attitudes toward certain issues.
Agree and strongly agree are considered as relatively similar responses while disagree and strongly disagree as similar responses. .
Percentage scores <50% are poor, 50%-75% moderate, and >75% good.
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from may 1 to septamber 30 2022
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Woldemichael, Wollo Universty
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 6525
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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