RecruitingNAINTERVENTIONAL

The Impact of Paramedic Training in Simulation on the Experience of Patients Treated for Malignant Brain Tumors in Neurosurgery (IPSIMANON)

This study, called IPSIMANON, is looking at how to make the experience better for adults who have just discovered they might have a brain tumour. Researchers want to see if giving special training to hospital staff (paramedics, though in this context it means healthcare professionals who support patients) helps patients feel more satisfied with their hospital stay. The training focuses on how to sensitively inform and support patients when they receive this news. Participants will be asked to fill out a questionnaire about their satisfaction with their hospital care at the end of their stay. The study hopes to find out if this training makes a real difference in how patients experience this challenging time.

At a glance

Status

Recruiting

Phase

Sponsor

University Hospital, Brest

Enrolment target

250

Start

15 May 2025

Estimated completion

01 Mar 2026

Brain Tumor Adult

What is this study about?

Imagine you've just been told you might have a brain tumour – that's incredibly difficult news. This study, called IPSIMANON, wants to make sure that when patients receive such life-changing information, they feel as supported and cared for as possible by the hospital staff.

The researchers are focusing on how hospital staff in neurosurgery departments – these are the doctors and nurses who look after brain and nerve conditions – talk to and support patients when a possible brain tumour is first found. They're trying out a special training programme for these staff members. This training uses 'simulation', which is like a practice run, to help staff learn the best ways to communicate and look after patients during such a sensitive time.

The main aim of the study is to see if patients who are cared for by these specially trained staff members feel more satisfied with their hospital experience compared to patients who receive standard care. To find this out, patients will be asked to complete a questionnaire about their hospital stay. The researchers hope that by improving the way staff communicate, patients will feel better supported and more positive about their overall care during a very challenging period.

Key takeaways

This study wants to improve how hospitals support patients with new brain tumour diagnoses.
It tests if special communication training for staff makes a difference to patient satisfaction.
Participation involves filling out a simple questionnaire at the end of your hospital stay.
The study has a low risk, as it focuses on gathering your feedback.
Your input could help improve care for many future patients.
Your medical treatment will not be affected by your participation.

Who may be eligible?

This study is looking for adults aged 18 or older who are receiving care under a social security scheme. You would be considered if you have just been diagnosed with a brain tumour, whether it's the first time you've had cancer or if it's a new tumour that needs checking.

To be part of the study, your brain tumour must have been found while you were already in the Neurosurgery Department of the hospital, before tests confirm exactly what type of tumour it is. You would also need to be able to understand and sign a consent form, showing you agree to take part.

However, you wouldn't be able to join the study if you have a history of other cancers. Also, if you don't have family or friends to support you AND you're unable to understand information about your condition, then this study might not be suitable for you.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

Are you 18 years old or older?
Are you covered by a social security scheme?
Have you recently been diagnosed with a brain tumour while in hospital?
Are you able to understand and sign a consent form?
Do you not have a personal history of other cancers?
Do you have family or friends to support you, or are you able to understand information about your condition?

Answer every question to see your result.

What does participation involve?

If you decide to take part in this study, your involvement will be quite simple. You won't need to take any new medication or have any extra procedures. At the very end of your hospital stay, you will be asked to fill out a questionnaire. This questionnaire is called the EORTC IN-PATSAT32 and it asks about your satisfaction with the care you received during your time in hospital. There are no follow-up visits or long-term assessments required after you leave the hospital for the purpose of this study. The total duration of your participation would be limited to completing this questionnaire at the end of your hospital stay.

Potential risks and benefits

Participating in this study involves a very low risk, as it simply asks for your thoughts on your hospital experience through a questionnaire. There are no physical risks involved. The potential benefits are mostly for future patients; your feedback could help improve communication training for healthcare staff, leading to better and more comforting experiences for others receiving difficult news. You are free to withdraw from the study at any time without giving a reason, and this will not affect your medical care.

Locations (11)

CHU Brest
Verified postcode
Brest, France· Not yet recruiting
CHU Amiens
Verified postcode
Amiens, France· Not yet recruiting
CHU Angers
Verified postcode
Angers, France· Not yet recruiting
CHU Bordeaux
Verified postcode
Bordeaux, France· Not yet recruiting
APHM Nord
Verified postcode
Marseille, France· Not yet recruiting
CHU Nantes
Verified postcode
Nantes, France· Not yet recruiting
CHU Nice
Verified postcode
Nice, France· Not yet recruiting
CHU Rouen
Verified postcode
Rouen, France· Not yet recruiting
CHU Saint Etienne
Verified postcode
Saint-Etienne, France· Recruiting
CHU Strasbourg
Verified postcode
Strasbourg, France· Not yet recruiting
CHU Tours
Verified postcode
Tours, France· Not yet recruiting

Common questions

What is the main goal of this study?

It aims to see if special training for hospital staff helps patients feel more satisfied when they find out they have a brain tumour.

Who are the 'paramedics' in this study?

In this study's context, 'paramedics' refers to healthcare staff in neurosurgery departments who support and communicate with patients.

What will I have to do if I join?

You will be asked to fill out a questionnaire about your satisfaction with your hospital care at the end of your stay.

Will taking part change my medical treatment?

No, participating in this study will not change your medical treatment or care in any way.

Can I stop participating if I change my mind?

Yes, you can choose to stop participating at any time, and it will not affect your care.

How to find out more

Doriane Gautier

doriane.gautier@chu-brest.fr +33 229 020 174 Official trial record

Always speak to your GP or specialist before deciding to take part in a study.