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Internet-Based Cognitive Behavioral Therapy for MRI-Related Anxiety

A Randomized Controlled Trial of Internet-Based Cognitive Behavioral Therapy for MRI-Related Anxiety

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07296822
Acronym
MRTightxiety
Enrollment
60
Registered
2025-12-22
Start date
2025-05-01
Completion date
2026-12-31
Last updated
2025-12-22

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

Conditions

Anxiety, Claustrophobia, Magnetic Resonance Imaging (MRI)

Brief summary

The aim of the study is to investigate whether internet-based cognitive behavioural therapy (iCBT) can help patients who have difficulty undergoing magnetic resonance imaging (MRI). The main question to be answered is \- Can patients undergo MRI with less anxiety using iCBT? The patients will undergo a four-week treatment that includes information about MRI, anxiety management, relaxation and retention. The end goal is to simulate an MRI scan in a mock scanner where participants can report their anxiety. Half of the participants will be randomized to receive the treatment before (intervention group) the simulated MRI scan and half will receive the treatment after the simulated MRI scan (control group). Up to 60 patients will be included plus some pilot patients.

Interventions

BEHAVIORALIntervention

Participants will receive the internet-based cognitive behavioral therapy (iCBT) intervention prior to undergoing the mock MR examination.

Sponsors

Linkoeping University
CollaboratorOTHER_GOV
Region Östergötland
CollaboratorOTHER
Region Jönköping County
CollaboratorOTHER_GOV
Landstinget i Kalmar Län
CollaboratorOTHER
Johan Kihlberg
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The patients will undergo a four-week treatment that includes information about MRI, anxiety management, relaxation and retention. The end goal is to simulate an MRI scan in a mock scanner where participants can report their anxiety. Half of the participants will be randomized to receive the treatment before (intervention group) the simulated MRI scan and half will receive the treatment after the simulated MRI scan (control group).

Eligibility

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

Inclusion criteria

* self-perceived problems with doing MRI examinations

Exclusion criteria

* difficulty understanding written text * severe mental health problems

Design outcomes

Primary

MeasureTime frameDescription
MRI-related anxietyBaseline and within two days of the mock MRI examinationMRI-related anxiety using the Magnetic Resonance Imaging Anxiety Questionnaire (MRI-AQ) measured before and after the mock MRI examination. Higher value means increased symptoms. Can give between 15-60 points.

Secondary

MeasureTime frameDescription
AnxietyBaseline and within two days of the mock MRI examinationAnxiety using Generalized Anxiety Disorder Seven Item Scale (GAD-7) measured before and after the mock MRI examination. Higher value means increased symptoms. Can give between 0-27 points.
ClaustrophobiaBaseline and within two days of the mock MRI examinationClaustrophobia using a Swedish validated translation of The Claustrophobia Questionnaire (CLQ) measured before and after the mock MRI examination. Higher value means increased symptoms. Can give between 0-48 points.
Mental healthBaseline and within two days of the mock MRI examinationMental health using the Patient Health Questionnaire-9 (PHQ-9) measured before and after the mock MRI examination. Higher value means increased symptoms. Can give between 0-27 points.

Countries

Sweden

Contacts

Primary ContactJohan Kihlberg, PhD
johan.kihlberg@liu.se+461038902
Backup ContactTomas Bjerner, PhD
tomas.bjerner@liu.se

Outcome results

None listed

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