Training Objectives AchievementNCT02205957
Training Quality in Anaesthesia and Intensive Care: Tunisian Residents Feed Back
An observational study of Training Objectives Achievement, run by University Hospital, Mahdia at 1 site in Tunisia.
Trial summary
Opinion survey to assess the level of satisfaction and the expectations of the residents in anesthesiology and intensive care in Tunisia ( North Africa) Read more about this study
- Who is it for?
- Ages 30 to 40 years
- Conditions the study is for
- Training Objectives Achievement
- How many people
- 160 participants
- Where
- 1 siteTunisia
- Study dates
- Jul 2014to Sep 2014
- 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 30 to 40 years
- All sexes
- No healthy volunteers
- Adult
Study population: Residents in anesthesiology and intensive care
Who may be able to join
- Tunisian nationality
- Resident in anesthesiology and intensive care
- training period : 6 months to four year
Who cannot join
- training done outside tunisia
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Training Quality in Anesthesia and Intensive Care : Tunisians Residents' Feed Back
Opinion survey to assess the level of satisfaction and the expectations of the residents in anesthesiology and intensive care in Tunisia ( North Africa)
Read the detailed description
The first national anonymous survey to assess the theoretical and practical training quality in anesthesia and intensive care and the improvements propositions.
- Conditions
- Training Objectives Achievement
- Keywords
- anesthesiology and intensive care, quality, training
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Training quality | Tunisian residents in anesthesiology and intensive care |
What is being measured
The primary outcome is the main question the study is designed to answer.
the approval of theoretical and practical teaching
A standardized questionnaire assessing the theoretical and practical training was distributed to the 1th,2th,3th and 4th-year anesthesiology residents
Measured: up to four year of training
Secondary outcomes (1)
Improvement propositions
residents can chose from different propositions and give other propositions if not listed in the questionnaire
Measured: up to 4th year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2014 (estimated)
- Study startJul 2014
- Primary completionAug 2014
- Study completionSep 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Training Objectives AchievementStudies of the same condition, open and under way.
- 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
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 160 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital, Mahdia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Majdoub Ali MD, University Hospital, Mahdia
- Investigators
- Kolsi Abdessalem, MD, Study director, Mahdia UNiversity Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02205957
- Sponsor's protocol ID
- Mah2014S1
- Status last verified
- Jan 2016
- First submitted
- 26 Jul 2014
- Last updated
- 14 Jan 2016
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 14 Jan 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Training Quality in Anesthesia and Intensive Care : Tunisians Residents' Feed Back
- ClinicalTrials.gov ID
- NCT02205957
- Acronym / sponsor ID
- Mah2014S1
- Conditions
- Training Objectives Achievement
- Keywords
- anesthesiology and intensive care, quality, training
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 160 participants (actual)
- Lead sponsor
- University Hospital, MahdiaUniversity, hospital or other
- Study start
- Jul 2014
- Primary completion
- Aug 2014 (actual)
- Study completion
- Sep 2014 (actual)
- First posted
- 1 Aug 2014 (estimated)
- 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.
Opinion survey to assess the level of satisfaction and the expectations of the residents in anesthesiology and intensive care in Tunisia ( North Africa)
Detailed description
The first national anonymous survey to assess the theoretical and practical training quality in anesthesia and intensive care and the improvements propositions.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Training quality | – | –Tunisian residents in anesthesiology and intensive care |
Who may qualify
- Ages
- 30 to 40 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- Residents in anesthesiology and intensive care
Key inclusion criteria (3 listed)
- Tunisian nationality
- Resident in anesthesiology and intensive care
- training period : 6 months to four year
Key exclusion criteria (1 listed)
- training done outside tunisia
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
the approval of theoretical and practical teaching
Time frame: up to four year of training
A standardized questionnaire assessing the theoretical and practical training was distributed to the 1th,2th,3th and 4th-year anesthesiology residents
1 secondary outcome
Improvement propositions
Time frame: up to 4th year
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 14 Jan 2016.
Related trials for Training Objectives Achievement
Not yet recruiting
Effects of Lokomat-Robot Assisted Gait Training on Gross Motor Function in Children and Young Adults With Cerebral Palsy
Cerebral Palsy
Not yet recruitingObservational study
Retrospective Study of Intensive Therapy Pathways in Children With Cerebral Palsy (P'TI-PARCOURS)
Cerebral Palsy, Hemiplegia
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.
Kolsi Abdessalem, MD study director
Mahdia UNiversity Hospital
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 Training Objectives Achievement, run by University Hospital, Mahdia at 1 site in Tunisia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Jan 2016. 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 Tunisia. 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?
the approval of theoretical and practical teaching (time frame: up to four year of training). 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 14 Jan 2016.