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Prediction of Claustrophobia During MR Imaging

Prediction of Claustrophobia During MR Imaging: An Observational 18-Months Single Center Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01367067
Acronym
CLAUSTRO II
Enrollment
8000
Registered
2011-06-06
Start date
2010-01-31
Completion date
2011-06-30
Last updated
2021-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Claustrophobia

Keywords

claustrophobia, magnetic resonance imaging, MRI, anxiety, anxious patients, phobic disorders, anxiety disorders, mental disorders

Brief summary

The objective of the study is to search for possible predictors for claustrophobia during magnetic resonance (MR) imaging. A claustrophobic event shall be defined by an incomplete examination, or a complete examination that requires coping actions by the staff. Coping actions may consist of the administration of sedatives, prism glasses, an MR imaging test run with the patient, a pause, the prone position, an escort in the scanner room, and supportive communication. The investigators hypothesize that there is a difference between patients with and without events in their scores on the Claustrophobia Questionnaire and several further psychometric questions. Other factors may also favour events like patient characteristics, examined region, duration of the examination and scanner type. Therefore, predictors could identify patients who are likely to experience claustrophobia during MR imaging so that they can receive the appropriate support by the staff to complete their examination. Thus a larger patient population could benefit from MR imaging.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Inpatients and outpatients referred to MR imaging with a clinical indication of any part of the body * Mentally and physically able to fill out a questionnaire * Sufficient German language skills

Exclusion criteria

* Age under 18 years * Patients from the Intensive Care Unit * Severe emergencies * Surgery during MR imaging * Participation in other studies * Fetal and prenatal examinations * Referral from medical jurisprudence

Design outcomes

Primary

MeasureTime frame
The mean score of the Claustrophobia Questionnaire for the prediction of a claustrophobic event during MR imagingUp to 5 min after the end of the MR

Secondary

MeasureTime frame
Identification of specific psychometric questions for the prediction of a claustrophobic event during MR imagingUp to 5 min after the end of the MR
Identification of influential factors for the prediction of a claustrophobic eventUp to 5 min after the end of the MR

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026