Intraosseous AccessNCT04918550
A Survey on the Cognition and Use of Intraosseous Access Among Medical Staff
An observational study of Intraosseous Access, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.
Trial summary
A Survey on the Cognition and Use of Intraosseous Access among Emergency Medical Staff, which is based on the platform of "WJX.CN", from January 5, 2018 to January 23, 2018, via local emergency-related academic organizations to emergency medical staff throughout the country. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Intraosseous Access
- What is being tested?
- no drug and device
- How many people
- 3,194 participants
- Where
- 1 siteChina
- Study dates
- 5 Jan 2018to 23 Jan 2018
- How long will I take part?
- 2 Weeks
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Medical staff of emergency medicine in china
Inclusion Criteria: 1) Emergency medical staff who have a Chinese medical practitioner certificate or a nurse practitioner certificate and are within the valid registration period; 2) Agree to participate in this study.
Exclusion Criteria: incomplete questionnaires.
Trial locations and contacts
1 site in 1 country.
China1 site
Department of Emergency Medicine, Second Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, 310000
About this study
Official title: A Survey on the Cognition and Use of Intraosseous Access Among Emergency Medical Staff
A Survey on the Cognition and Use of Intraosseous Access among Emergency Medical Staff, which is based on the platform of "WJX.CN", from January 5, 2018 to January 23, 2018, via local emergency-related academic organizations to emergency medical staff throughout the country. There are 3 sections in the questionnaire: the demographic information of the participants; cognition levels and clinical use of IO; barriers and attitudes towards clinical use of IO including willingness, confidence and training demand.
Read the detailed description
This research is a cross-sectional survey research, using the method of network survey, with domestic emergency medicine medical staff as the research object. Inclusion criteria: 1) Emergency medical staff who have a Chinese medical practitioner certificate or a nurse practitioner certificate and are within the valid registration period; 2) Agree to participate in this study. Exclusion criteria: incomplete questionnaires. The questionnaire was designed for the "Survey of Current Status of Marrow Cavity Pathway Cognition of Medical Staff in Emergency Department", including three parts: (1) general information of the survey object; (2) cognition and use status of IO; (3) clinical application of IO Attitude. Based on the "Questionnaire Star" platform, questionnaires are distributed through various emergency-related academic organizations. The front page of the questionnaire clearly marked the reminder of voluntary participation in the survey and related declarations, and it could be filled out after informed consent.
- Conditions
- Intraosseous Access
- Being tested
- no drug and device
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
no drug and deviceOther
there is no intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Cognition levels and clinical use of IO
Cognitive level is divided into: never heard of, heard of, equipped, used
Measured: two weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jun 2021
- Study start5 Jan 2018
- Primary completion23 Jan 2018
- Study completion23 Jan 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Intraosseous AccessStudies of the same condition, open and under way.
- More trials run by Second Affiliated Hospital, Zhejiang University, School of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 3,194 participants (actual)
- Target duration
- 2 Weeks
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04918550
- Sponsor's protocol ID
- 2021-0396
- Status last verified
- Jun 2021
- First submitted
- 2 Jun 2021
- Last updated
- 9 Jun 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: no share
Study at a glance
From the registry record, last updated by the sponsor on 9 Jun 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Survey on the Cognition and Use of Intraosseous Access Among Emergency Medical Staff
- ClinicalTrials.gov ID
- NCT04918550
- Acronym / sponsor ID
- 2021-0396
- Conditions
- Intraosseous Access
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 3,194 participants (actual)
- Lead sponsor
- Second Affiliated Hospital, Zhejiang University, School of MedicineUniversity, hospital or other
- Study start
- 5 Jan 2018 (actual)
- Primary completion
- 23 Jan 2018 (actual)
- Study completion
- 23 Jan 2018 (actual)
- First posted
- 9 Jun 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A Survey on the Cognition and Use of Intraosseous Access among Emergency Medical Staff, which is based on the platform of "WJX.CN", from January 5, 2018 to January 23, 2018, via local emergency-related academic organizations to emergency medical staff throughout the country. There are 3 sections in the questionnaire: the demographic information of the participants; cognition levels and clinical use of IO; barriers and attitudes towards clinical use of IO including willingness, confidence and training demand.
Detailed description
This research is a cross-sectional survey research, using the method of network survey, with domestic emergency medicine medical staff as the research object. Inclusion criteria: 1) Emergency medical staff who have a Chinese medical practitioner certificate or a nurse practitioner certificate and are within the valid registration period; 2) Agree to participate in this study. Exclusion criteria: incomplete questionnaires. The questionnaire was designed for the "Survey of Current Status of Marrow Cavity Pathway Cognition of Medical Staff in Emergency Department", including three parts: (1) general information of the survey object; (2) cognition and use status of IO; (3) clinical application of IO Attitude. Based on the "Questionnaire Star" platform, questionnaires are distributed through various emergency-related academic organizations. The front page of the questionnaire clearly marked the reminder of voluntary participation in the survey and related declarations, and it could be filled out after informed consent.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Target follow-up
- 2 Weeks
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Medical staff of emergency medicine in china
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| no drug and devicethere is no intervention | Other | – |
Primary outcome
Cognition levels and clinical use of IO
Time frame: two weeks
Cognitive level is divided into: never heard of, heard of, equipped, used
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Jun 2021.
- Individual participant dataSharing planned: No. no share
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Intraosseous Access, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.
The full registered description is in the About this study section and the official record.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 9 Jun 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cognition levels and clinical use of IO (time frame: two weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jun 2021.