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RecruitingNCT07296822MRTightxietyUpdated Dec 22, 2025

Internet-Based Cognitive Behavioral Therapy for MRI-Related Anxiety

An interventional study of Intervention in Anxiety, Claustrophobia and Magnetic Resonance Imaging (MRI), sponsored by Johan Kihlberg. Recruiting at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-22.

Sponsored by Johan Kihlberg · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as recruiting.
  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Anxiety
  • Claustrophobia
  • Magnetic Resonance Imaging (MRI)

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03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's planned enrollment of 60 is below the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

This is the only study on the registry with Johan Kihlberg as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • self-perceived problems with doing MRI examinations

Exclusion criteria

Exclusion Criteria:

  • difficulty understanding written text
  • severe mental health problems
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • No intervention
    Controls

    Participants will receive the same iCBT intervention after completing the mock MR examination.

  • Experimental
    Intervention

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

    Behavioral: Intervention

Interventions

  • BehavioralIntervention

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

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What researchers measure

Primary outcomes

  1. MRI-related anxiety

    MRI-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.

    Time frame: Baseline and within two days of the mock MRI examination

Secondary outcomes

  1. Anxiety

    Anxiety 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.

    Time frame: Baseline and within two days of the mock MRI examination

  2. Claustrophobia

    Claustrophobia 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.

    Time frame: Baseline and within two days of the mock MRI examination

  3. Mental health

    Mental 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.

    Time frame: Baseline and within two days of the mock MRI examination

07

Study locations

1 of 1 sites recruiting
  • Linköping University
    Linköping, 58739, Sweden
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Collected data will be stored at Linköping University, which the entire research group has full access to. No unauthorized persons will have access to the data. This is a research project with a quantitative method where the results are reported in aggregated form. The data is reported completely anonymized and only at the group level.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07296822
Lead sponsor
Johan Kihlberg
Collaborators
Linkoeping University, Region Östergötland, Region Jönköping County, Landstinget i Kalmar Län
Responsible party
Johan Kihlberg (Associate Professor, Linkoeping University) — Sponsor-investigator
First posted
Dec 22, 2025
Start date
May 1, 2025
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Dec 22, 2025

Study contacts

Johan Kihlberg, PhD
Contact
johan.kihlberg@liu.se
+461038902
Tomas Bjerner, PhD
Contact
tomas.bjerner@liu.se

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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