Patient SatisfactionNCT05765799
Evaluation of Patient Information in Interventional Radiology.
An observational study of Patient Satisfaction, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.
Trial summary
Interventional radiology is developing. Patient information modalities are also evolving, in particular information videos. The aim of this work is therefore the evaluation of patient information in interventional radiology Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Patient Satisfaction
- What is being tested?
- Questionary
- How many people
- 100 participants
- Where
- 1 siteFrance
- Study dates
- 1 Dec 2021to Jan 2025
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Any patient who receives a consultation before an interventional procedure will be included.
Who may be able to join
- Any patient who receives a consultation before an interventional procedure.
Who cannot join
- None
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
Chu Saint-Etienne
Saint-Etienne
Sylvain Grange, MD
Rémi Grange, MD
About this study
Interventional radiology is developing. Patient information modalities are also evolving, in particular information videos.
The aim of this work is therefore the evaluation of patient information in interventional radiology
- Conditions
- Patient Satisfaction
- Being tested
- Questionary
- Keywords
- interventional radiology, Information, videos
- Medical subject headings
- Patient Satisfaction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
QuestionaryOther
Questionary will be administrated to evaluated the information for patients on interventional radiology (dedicated consultation, information posters, explanatory video, information form, etc.).
| Study group | Role | What they receive |
|---|---|---|
| Patient who receives a consultation before an interventional procedure | Any patient who receives a consultation before an interventional procedure will be included. Questionary will be administrated. Receives: Other: Questionary |
What is being measured
The primary outcome is the main question the study is designed to answer.
To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist
Analysis results of questionary.
Measured: Year : 2
To evaluate Effectiveness of each patient information tool by Consultation with another doctor who explained the procedure
Analysis results of questionary.
Measured: Year : 2
To evaluate Effectiveness of each patient information tool by Explanatory videos
Analysis results of questionary.
Measured: Year : 2
To evaluate Effectiveness of each patient information tool by Patient information sheet
Analysis results of questionary.
Measured: Year : 2
To evaluate Effectiveness of each patient information tool by Posters in the consultation room
Analysis results of questionary.
Measured: Year : 2
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Mar 2023
- Study start1 Dec 2021
- Primary completionJan 2025 (estimated)
- Study completionJan 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patient SatisfactionStudies of the same condition, open and under way.
- More trials run by Centre Hospitalier Universitaire de Saint EtienneThe 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Sylvain GRANGE, MD, Principal investigator, Centre Hospitalier Universitaire de Saint Etienne
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05765799
- Sponsor's protocol ID
- IRBN1482021/CHUSTE
- Status last verified
- Apr 2024
- First submitted
- 27 Feb 2023
- Last updated
- 11 Apr 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Patient Information in Interventional Radiology.
- ClinicalTrials.gov ID
- NCT05765799
- Acronym / sponsor ID
- IRBN1482021/CHUSTE
- Conditions
- Patient Satisfaction
- Keywords
- interventional radiology, Information, videos
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Centre Hospitalier Universitaire de Saint EtienneUniversity, hospital or other
- Study start
- 1 Dec 2021 (actual)
- Primary completion
- Jan 2025 (estimated)
- Study completion
- Jan 2025 (estimated)
- First posted
- 13 Mar 2023 (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.
Interventional radiology is developing. Patient information modalities are also evolving, in particular information videos.
The aim of this work is therefore the evaluation of patient information in interventional radiology
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patient who receives a consultation before an interventional procedure | – | Other: QuestionaryAny patient who receives a consultation before an interventional procedure will be included. Questionary will be administrated. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Any patient who receives a consultation before an interventional procedure will be included.
Key inclusion criteria (1 listed)
- Any patient who receives a consultation before an interventional procedure.
Key exclusion criteria (1 listed)
- None
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 |
|---|---|---|
| QuestionaryQuestionary will be administrated to evaluated the information for patients on interventional radiology (dedicated consultation, information posters, explanatory video, information form, etc.). | Other | Patient who receives a consultation before an interventional procedure |
Primary outcome
To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist
Time frame: Year : 2
Analysis results of questionary.
To evaluate Effectiveness of each patient information tool by Consultation with another doctor who explained the procedure
Time frame: Year : 2
Analysis results of questionary.
To evaluate Effectiveness of each patient information tool by Explanatory videos
Time frame: Year : 2
Analysis results of questionary.
To evaluate Effectiveness of each patient information tool by Patient information sheet
Time frame: Year : 2
Analysis results of questionary.
To evaluate Effectiveness of each patient information tool by Posters in the consultation room
Time frame: Year : 2
Analysis results of questionary.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Apr 2024.
- Individual participant dataSharing planned: No
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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.
Sylvain GRANGE, MD principal investigator
Centre Hospitalier Universitaire de Saint Etienne
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 Patient Satisfaction, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.
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 1 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: status not confirmed, as of the sponsor's last update on 11 Apr 2024. 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 France. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Sylvain GRANGE, MD ((0)477127827 ext. +33, Sylvain.Grange@chu-st-etienne.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To evaluate effectiveness of each patient information tool by Consultation with the interventional radiologist (time frame: Year : 2). The study lists 5 primary outcomes in all. 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 11 Apr 2024.