How effective is a preparatory video in reducing fear and anxiety among patients undergoing magnetic resonance imaging?

ISRCTN ISRCTN15794750
DOI https://doi.org/10.1186/ISRCTN15794750
Sponsor King Khalid University
Funder Deanship of Scientific Research, King Khalid University
Submission date
21/07/2026
Registration date
27/07/2026
Last edited
24/07/2026
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Moawia Gameraddin
Scientific, Public, Principal investigator

King Mohammed Bin Abdulaziz
Alrabawa
Al-Madinah
42353
Saudi Arabia

Phone +966 (0)534821130
Email gameraldinm@gmail.com

Study information

Primary study designInterventional
AllocationRandomized controlled trial
MaskingBlinded (masking used)
ControlActive
AssignmentParallel
PurposeHealth services research
Scientific titleEffectiveness of video-based preparation in reducing anxiety and improving outcomes in mri: a prospective experimental study
Study objectives Primary objective:
To evaluate the effectiveness of a video-based educational preparation in reducing anxiety among adult patients undergoing magnetic resonance imaging (MRI) compared with standard verbal preparation

Secondary objectives:
1. To compare patient cooperation during MRI between the intervention and control groups
2. To assess patient movement during MRI scanning
3. To evaluate the need for repeat MRI examinations due to patient movement
4. To assess patients' understanding of the MRI procedure and the clarity of the preparation provided
5. To evaluate patients' perceptions of the educational video, including its helpfulness, effect on confidence, and understanding of the MRI examination
Ethics approval(s)

1. Approved 26/02/2026, The Research Ethics Committee at King Khalid University (HAPO-06-B-001) (King Khalid University, Abha, 61421, Saudi Arabia; 0172417484; ecm@kku.edu.sa), ref: KKU-60-2026-1

2. Approved 26/02/2026, The Research Ethics Committee at King Khalid University (HAPO-06-B-001) (King Khalid University , Abha, Aseer, Kingdom of Saudi Arabia., Abha, 61421, Saudi Arabia; 0172417484.; ecm@kku.edu.sa), ref: KKU-60-2026-1

Health condition(s) or problem(s) studiedMagnetic resonance imaging (MRI)-related anxiety in adult patients undergoing MRI examinations
InterventionIntervention arm 1 (experimental group):
Video-based educational preparation before MRI:
Participants received a standardized educational video immediately before undergoing magnetic resonance imaging (MRI). The video explained the MRI procedure, scanner environment, examination duration, expected acoustic noise, patient positioning, contraindications, and the importance of remaining still throughout the examination. Following the video, participants proceeded with the MRI examination and completed the study questionnaires, as follows:

Experimental group:
Participants viewed a standardized educational video immediately before the MRI. The video explained the MRI procedure, expected noise, examination duration, patient positioning, contraindications, and the importance of remaining still during image acquisition. Following the intervention, participants underwent MRI and completed study questionnaires.

Control group:
Participants received routine verbal preparation according to standard clinical practice before MRI without viewing the educational video. They subsequently underwent MRI and completed the same study assessments.

Method of randomization:
Participants were randomly allocated to either the intervention or control group using a computer-generated allocation sequence. Allocation concealment was ensured using sequentially numbered, sealed, opaque envelopes, which were opened only after participant enrolment.
Intervention typeBehavioural
Primary outcome measure(s)
  1. MRI-related anxiety measured using Visual Analogue Scale (VAS) at immediately before and immediately after MRI examination
Key secondary outcome measure(s)
Completion date02/04/2026

Eligibility

Participant type(s)
Age groupAdult
Lower age limit20 Years
Upper age limit60 Years
SexAll
Target sample size at registration251
Total final enrolment231
Key inclusion criteria1. Adults aged 20 years or older
2. Patients scheduled to undergo a magnetic resonance imaging examination at the study site
3. Able to understand the study information and the educational video
4. Able and willing to provide informed consent
5. Able to complete the study questionnaire before and/or after the MRI examination
Key exclusion criteria1. Patients younger than 20 years or older than 60 years (if these were the predefined age limits)
2. Patients unable to provide informed consent
3. Patients with cognitive impairment or communication difficulties that prevented understanding of the educational video or completion of the questionnaire
4. Patients requiring emergency MRI examinations where there was insufficient time to receive the preparatory intervention
5. Patients who declined participation in the study
6. Patients unable to complete the study questionnaire
Date of first enrolment18/03/2026
Date of final enrolment27/03/2026

Locations

Countries of recruitment

  • Saudi Arabia

Study participating centres

Results and Publications

Individual participant data (IPD) Intention to shareNo

Editorial Notes

21/07/2026: Study's existence confirmed by the Research Ethics Committee at King Khalid University.