Register new project at CIR

Before you register a new project make sure you have read and understood the road map for projects at CIR and the user agreement details.

Road map for projects at CIR
Road map for imaging projects at CIR Photo: N/A

Road map for projects at CIR

A great first step to your project is to go over the road map of a typical project at CIR. This will provide with a general timeline and some valid checkpoints to aim for.

User agreement details
Illustration of checklist before agreement Photo: N/A

User agreement details

Read through the user agreement details to learn what responsibilities come with running an imaging project at CIR.

Project name

CIR will also create and provide you with a unique project identifier used to track projects.

Brief project description

Will another researcher than the PI be managing the project at CIR?

Contact details for the project's Principal Investigator (PI)

Contact details for the researcher managing the project at CIR

Pre-clinical

Is this a pre-clinical project, involving imaging of animal models?

User agreement

Data access and sharing

It is the ultimate responsibility of the projects PI to ensure that only researchers that need access to the projects data have access and follow the KI guidelines for research documentation and data management. It is possible, but inappropriate, for any user with access to a project folder on SPICE to download, copy or distribute its content - this is outside the control of CIR.

Data storage

The Shared Platform for Imaging in the CIR Environment (SPICE) is offered as an analysis space for active projects, but is not backed-up long term storage. It is the responsibility of each projects PI to ensure data is backed-up and archived.

Human participants

It is the responsibility of the researcher in charge of scanning to confirm that the participant has a valid Swedish personal identity number (personnummer)

Authorship

The projects PI has the ultimate responsibility for keeping track of contributions made throughout the project in accordance with the authorship guidelines in the user agreement details.

Does the PI or managing researcher have a user account on the CIR server (SPICE)?

For example if they are connected to other projects at CIR.

Project start date (approx.)

Project end date (approx)

Ethical approval

Has ethical approval been awarded for the suggested project?

Ethical registry number/DNR

Upload ethical permit (pdf)


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Main purpose of data acquisition

Main study population of the project

What kind of clinical patient/diagnosis?

(Example: PD, AD, Epilepsy, MDD)

How many subjects do you plan to include?

Age range of participants (years)

From age:
To age:

Imaging modalities and core facilities planned for use in project

What size EEG array will you use?

Stimulation modalities used in experiment?

Auxiliary measurements during scanning?

What radioligand(s) will be used?

Researchers responsible for the different parts of the project

Responsible for setting up experiments and protocol

 

Responsible for performing pilot measurements

 

Responsible for data acquisition

 

Responsible for data analysis

 

Responsible for manuscript/publication

Project description

The information given in this form is correct, complete and will be updated if changes occur in the project.

Signature of PI or managing researcher

Digital signature in grey area below.