PreoperativeNCT00864695
Role of Anesthesiologist-Patient Relationship
An observational study of Preoperative and Anesthesia, run by UPECLIN HC FM Botucatu Unesp at 1 site in Brazil.
Trial summary
Descriptive analytic survey of 1137 and 518 patients aged 16 years or more before and after anesthesia exposure, respectively to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist. Read more about this study
- Who is it for?
- Ages 16 years and olderHealthy volunteers can take part
- Conditions the study is for
- Preoperative, Anesthesia, Postoperative
- What is being tested?
- Supportive care
- How many people
- 1,137 participants
- Where
- 1 siteBrazil
- Study dates
- May 2007to May 2008
- 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 16 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: This descriptive-analytic study was based on opinions and information provided before and after anesthesia by individuals who were hospitalized in the Botucatu Medical School Hospital to undergo surgery under anesthesia. A questionnaire was used to determine patient characteristics and perception of anesthesia/anesthesiologist, as well as fears and concerns related to anesthesia.
Who may be able to join
- conscious surgical patients
- 16 years or more
- Portuguese-speaking patients
Who cannot join
- patients with altered states of consciousness or expression/comprehension impairment
- patients who did not undergo anesthesia/surgery (cancelled or postponed)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Role of Anesthesiologist-Patient Relationship in Changing Postoperative Perception of Patients Admitted to a Teaching Hospital
Descriptive analytic survey of 1137 and 518 patients aged 16 years or more before and after anesthesia exposure, respectively to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist. The aim of this study was to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist.
Period: may/2007 to may/2008
Read the detailed description
A questionnaire was used to determine patient characteristics and perception of anesthesia/anesthesiologist, as well as fears and concerns related to anesthesia. This descriptive-analytic study was based on opinions and information provided before and after anesthesia by individuals who were hospitalized in the Botucatu Medical School (BMS) Hospital to undergo surgery under anesthesia administered by the Anesthesiology Service of BMS Department of Anesthesiology. A questionnaire including structured questions aimed at determining patient characteristics (age, gender, race, marital status, education level, birthplace, provenance, surgical service of origin, occupation, history of anesthesia exposure) and perceptions of anesthesiologists/anesthesia, as well as open-ended questions that allowed respondents to add free comments, recorded as spoken, about their concerns before and after anesthesia. The post-anesthesia interview also included questions regarding the administration of pre-anesthetic drugs, recall of the anesthesiologist in the operating room, satisfaction with the care provided by the anesthesiologist.
- Conditions
- Preoperative, Anesthesia, Postoperative
- Being tested
- Supportive care
- Keywords
- Anesthesia, Ethics, Trends, Manpower, Perioperative care
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Supportive careOther
Also called Questionnaire
protocol designed to evaluate one or more interventions where the primary intent is to maximize comfort, minimize side effects or mitigate against a decline in the subject's health or function. In general, supportive care interventions are not intended to cure a disease.
| Study group | Role | What they receive |
|---|---|---|
| Surgical patients | Individuals who were hospitalized in the Botucatu Medical School Hospital to undergo surgery under anesthesia administered by the Anesthesiology Service of BMS Department of Anesthesiology. Receives: Other: Supportive care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Role of anesthesiologist-patient relationship in changing postoperative perception of patients admitted to a teaching hospital
Measured: one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Mar 2009 (estimated)
- Study startMay 2007
- Primary completionMay 2008
- Study completionMay 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PreoperativeStudies 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
- Prospective
- Enrolment
- 1,137 participants (actual)
Sponsor and investigators
- Lead sponsor
- UPECLIN HC FM Botucatu Unesp
- Sponsor type
- University, hospital or other
- Collaborators
- Faculdade de Medicina de Botucatu, UNESP, Botucatu, Brasil, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
- Investigators
- Fernanda Leite, Principal investigator, College Study of Medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00864695
- Sponsor's protocol ID
- upeclin/HC/FMB-Unesp-21
- Status last verified
- Mar 2009
- First submitted
- 18 Mar 2009
- Last updated
- 19 Mar 2009
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 19 Mar 2009. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Role of Anesthesiologist-Patient Relationship in Changing Postoperative Perception of Patients Admitted to a Teaching Hospital
- ClinicalTrials.gov ID
- NCT00864695
- Acronym / sponsor ID
- upeclin/HC/FMB-Unesp-21
- Conditions
- Preoperative, Anesthesia, Postoperative
- Keywords
- Anesthesia, Ethics, Trends, Manpower, Perioperative care
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,137 participants (actual)
- Lead sponsor
- UPECLIN HC FM Botucatu UnespUniversity, hospital or other
- Collaborators
- Faculdade de Medicina de Botucatu, UNESP, Botucatu, Brasil, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
- Study start
- May 2007
- Primary completion
- May 2008 (actual)
- Study completion
- May 2008 (actual)
- First posted
- 19 Mar 2009 (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.
Descriptive analytic survey of 1137 and 518 patients aged 16 years or more before and after anesthesia exposure, respectively to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist. The aim of this study was to assess the anesthesiologist-patient relationship role on patient postoperative perception of the binominal anesthesia-anesthesiologist.
Period: may/2007 to may/2008
Detailed description
A questionnaire was used to determine patient characteristics and perception of anesthesia/anesthesiologist, as well as fears and concerns related to anesthesia. This descriptive-analytic study was based on opinions and information provided before and after anesthesia by individuals who were hospitalized in the Botucatu Medical School (BMS) Hospital to undergo surgery under anesthesia administered by the Anesthesiology Service of BMS Department of Anesthesiology. A questionnaire including structured questions aimed at determining patient characteristics (age, gender, race, marital status, education level, birthplace, provenance, surgical service of origin, occupation, history of anesthesia exposure) and perceptions of anesthesiologists/anesthesia, as well as open-ended questions that allowed respondents to add free comments, recorded as spoken, about their concerns before and after anesthesia. The post-anesthesia interview also included questions regarding the administration of pre-anesthetic drugs, recall of the anesthesiologist in the operating room, satisfaction with the care provided by the anesthesiologist.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Surgical patients | – | Other: Supportive careIndividuals who were hospitalized in the Botucatu Medical School Hospital to undergo surgery under anesthesia administered by the Anesthesiology Service of BMS Department of Anesthesiology. |
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- This descriptive-analytic study was based on opinions and information provided before and after anesthesia by individuals who were hospitalized in the Botucatu Medical School Hospital to undergo surgery under anesthesia. A questionnaire was used to determine patient characteristics and perception of anesthesia/anesthesiologist, as well as fears and concerns related to anesthesia.
Key inclusion criteria (3 listed)
- conscious surgical patients
- 16 years or more
- Portuguese-speaking patients
Key exclusion criteria (2 listed)
- patients with altered states of consciousness or expression/comprehension impairment
- patients who did not undergo anesthesia/surgery (cancelled or postponed)
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 |
|---|---|---|
| Supportive careAlso: Questionnaireprotocol designed to evaluate one or more interventions where the primary intent is to maximize comfort, minimize side effects or mitigate against a decline in the subject's health or function. In general, supportive care interventions are not intended to cure a disease. | Other | Surgical patients |
Primary outcome
Role of anesthesiologist-patient relationship in changing postoperative perception of patients admitted to a teaching hospital
Time frame: one 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 19 Mar 2009.
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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.
Fernanda Leite principal investigator
College Study of Medicine
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 Preoperative and Anesthesia, run by UPECLIN HC FM Botucatu Unesp at 1 site in Brazil.
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 2 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 19 Mar 2009. 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 Brazil. 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?
Role of anesthesiologist-patient relationship in changing postoperative perception of patients admitted to a teaching hospital (time frame: one year). 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 19 Mar 2009.