Date of filling in this questionnaire or last update: 10/07/2020
1. IDENTIFICATION & BASIC DESCRIPTION
Cohort name
  MRI workers and subjective symptoms
Country
 

  • Italy

Name
  Fabriziomaria Gobba
Institution
  Università degli studi di Modena e Reggio Emilia
Email
  fabriziomaria.gobba@unimore.it
Phone
  +390592055463
Do you want to add another Principal Investigator of the Cohort
 

  • Add another Principal Investigator of the cohort

Name
  Alberto Modenese
Institution
  Università degli studi di Modena e Reggio Emilia
Email
  alberto.modenese@unimore.it
Phone
  +390592055475
Name of committee
  Province of Modena (Italy)
Upload files
 

Contact Principal Investigator (name)
  Alberto Modenese
Data access policy (briefly describe)
  Full access to anonymous data on MRI operators form Italy and possible sensorial symptoms (e.g. vertigo)
Upload files
 

Participation in pooled analyses
 

  • The cohort is potentially interested in participating in pooled analyses of (European) occupational cohort studies (note pooled analyses also includes remote decentralized analyses that would not require any transfer of primary data as well as meta-analyses).

Main aim of cohort, please briefly describe the main objectives of the cohort
  Investigate occupational exposure of MRI operators to EMF and possible related subjective sensorial symptoms
Study design (please select as many as appropriate)
 

  • Prospective cohort
  • Retrospective cohort

Source population (please select as many as appropriate)
 

  • Industry / occupation-based

Comparators (please select as many as appropriate)
 

  • Internal study population

Inclusion criteria
  MRI operators, working age
Exclusion criteria
  Control group: same job category of exposed group, same hospital department, no MRI exposure
Enrollment
  Ongoing
Age range at entry (main cohort)
 

Minimum Maximum Mean
25 70 45

Men at enrollment
  131
Women at enrollment
  153
Children (<18 years) at enrollment
  0
Men at last follow-up
  0
Women at last follow-up
  0
Children (<18 years) at last follow-up
  0
Participation rate at enrollment (if known)
  70
2. OUTCOME FOLLOW-UP
Type of data for outcome follow-up (please select as many as appropriate)
 

  • Active (contact with participants)

Active (contact with participants) (specify)
 

  • Questionnaire to investigate exposure and symptoms

First follow-up period (provide year)
  to be defined
Last follow-up period (provide year)
  to be defined
Number of follow-ups after baseline (provide number)
  to be defined
3. OCCUPATIONAL EXPOSURES
Source of exposure data collected (please select as many as appropriate)
 

  • Questionnaire, Personal (Self-reporting or interview)
  • Job-employment records

Occupational history/time frame
  Lifetime
Occupational coding performed
  No
Methods for exposure assessment (please select as many as appropriate)
 

  • Expert assessment
  • Self-report

Main categories
 

  • Physical agents

Physical agents
 

  • Radiation

Physical agents | Radiation
 

  • Non-ionising