A Protocol for a Virtual Reality Exposure Therapy for Fear of Flying.

Sponsor
University of Barcelona (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05939986
Collaborator
(none)
84
1
3
5
16.8

Study Details

Study Description

Brief Summary

This study aims to assess whether adding vibrotactile stimulation to visual and auditory stimulation increases the efficacy of VRET for FoF treatment. Eighty-four participants (18-65 years old) will be assigned to one of three intervention arms, namely the VRET with multimodal feedback (visual, auditory, and vibrotactile; VRET-M), the VRET with bimodal feedback (visual and auditory; VRET-B), or the imagery exposure treatment (IET) without sensory feedback. FoF-related symptoms (primary outcomes) will be measured administering the Fear of Flying Questionnaire-II (QPV-II), the Fear of Flying Scale (FFS), and the Visual Analogic Scale (VAS-A) before and after eight sessions of treatment, and at six- and 12-month follow-ups. Anxiety and the sense of presence experienced during exposure sessions (secondary outcome measures: VAS-A and VAS-P) will also be assessed. It is expected that participants in the VRET-M group will report a further reduction of FoF-related symptomatology after the treatment and at follow-ups compared to participants in the VRET-B and IET groups. Likewise, participants in the VRET-M group are expected to show higher sense of presence levels during exposure sessions in comparison to participants in the VRET-B and IET groups. It is expected that the IET group will report the lowest level of sense of presence and the poorest outcome after treatment and at follow-ups.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Virtual reality-based exposure treatment with multimodal feedback (VRET-M)
  • Behavioral: Virtual reality-based exposure treatment with bimodal feedback (VRET-B)
  • Behavioral: Imagery exposure treatment (IET)
N/A

Detailed Description

Participants who meet the inclusion criteria will be invited to participate in the initial treatment session. They will be also required to purchase a flight ticket during the six months after the end of the treatment. Participants will be treated weekly for eight individual sessions. While the first two sessions involve preparation and training, exposure will be conducted between the third and eighth session. The exposure sessions' structure and content will be the same in all conditions. Nevertheless, the VRET-M group will experience vibrotactile cues, while the VRET-B group will not. Furthermore, the IET group will experience its own subjective imagined environment without any external stimulation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
84 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be assigned to one of three intervention arms, namely the VRET with multimodal feedback (visual, auditory, and vibrotactile; VRET-M), the VRET with bimodal feedback (visual and auditory; VRET-B), or the imagery exposure treatment (IET).Participants will be assigned to one of three intervention arms, namely the VRET with multimodal feedback (visual, auditory, and vibrotactile; VRET-M), the VRET with bimodal feedback (visual and auditory; VRET-B), or the imagery exposure treatment (IET).
Masking:
None (Open Label)
Masking Description:
Not-blinded study protocol.
Primary Purpose:
Treatment
Official Title:
Virtual Reality Exposure Therapy for Fear of Flying: Protocol for a Randomized Controlled Trial
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Oct 15, 2023
Anticipated Study Completion Date :
Jan 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Multimodal Virtual Reality Exposure Treatment (VRET-M)

VRET with multimodal feedback including visual, auditory and vibrotactile cues.

Behavioral: Virtual reality-based exposure treatment with bimodal feedback (VRET-B)
The VRET-B group will experience visual and auditive cues in the exposure sessions.

Behavioral: Imagery exposure treatment (IET)
The IET group will experience its own subjective imagined environment without any external stimulation.

Active Comparator: Bimodal Virtual Reality Exposure Treatment (VRET-B)

VRET with bimodal feedback including visual and auditory cues.

Behavioral: Virtual reality-based exposure treatment with multimodal feedback (VRET-M)
The VRET-M group will experience visual, auditive and vibrotactile cues in the exposure sessions.

Behavioral: Imagery exposure treatment (IET)
The IET group will experience its own subjective imagined environment without any external stimulation.

Active Comparator: Imagery Exposure Treatment (IET)

Imagery exposure treatment without sensory cues.

Behavioral: Virtual reality-based exposure treatment with multimodal feedback (VRET-M)
The VRET-M group will experience visual, auditive and vibrotactile cues in the exposure sessions.

Behavioral: Virtual reality-based exposure treatment with bimodal feedback (VRET-B)
The VRET-B group will experience visual and auditive cues in the exposure sessions.

Outcome Measures

Primary Outcome Measures

  1. Fear of Flying (FoF). Administering the Fear of Flying Questionnaire-II (QPV-II) and the Fear of Flying Scale (FFS). [Before the exposure treatment.]

    To what extend I feel fear about flying by plane? The QPV-II is rated from on a 10-point scale (0 = absence of anxiety, 10 = extreme anxiety) with scores ranging from 0 to 300. The FFS is rated on a 5-point scale (0 = not at all, 4 = very much), with scores ranging from 0 to 84.

  2. Fear of Flying (FoF). Administering the Fear of Flying Questionnaire-II (QPV-II) and the Fear of Flying Scale (FFS). [After eight sessions of treatment during eight weeks.]

    To what extend I feel fear about flying by plane? The QPV-II is rated from on a 10-point scale (0 = absence of anxiety, 10 = extreme anxiety) with scores ranging from 0 to 300. The FFS is rated on a 5-point scale (0 = not at all, 4 = very much), with scores ranging from 0 to 84.

  3. Fear of Flying (FoF). Administering the Fear of Flying Questionnaire-II (QPV-II) and the Fear of Flying Scale (FFS). [At 6 months follow-up after treatment termination.]

    To what extend I feel fear about flying by plane? The QPV-II is rated from on a 10-point scale (0 = absence of anxiety, 10 = extreme anxiety) with scores ranging from 0 to 300. The FFS is rated on a 5-point scale (0 = not at all, 4 = very much), with scores ranging from 0 to 84.

  4. Fear of Flying (FoF). Administering the Fear of Flying Questionnaire-II (QPV-II) and the Fear of Flying Scale (FFS). [At 12 months follow-up after treatment termination.]

    To what extend I feel fear about flying by plane? The QPV-II is rated from on a 10-point scale (0 = absence of anxiety, 10 = extreme anxiety) with scores ranging from 0 to 300. The FFS is rated on a 5-point scale (0 = not at all, 4 = very much), with scores ranging from 0 to 84.

  5. Anxiety. Administering a Visual Analogue Scale (VAS-A). [Before the exposure treatment.]

    To what extend I feel anxious about flying by plane? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  6. Anxiety. Administering a Visual Analogue Scale (VAS-A). [After eight sessions of treatment during eight weeks.]

    To what extend I feel anxious about flying by plane? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  7. Anxiety. Administering a Visual Analogue Scale (VAS-A). [At 6 months follow-up after treatment termination.]

    To what extend I feel anxious about flying by plane? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  8. Anxiety. Administering a Visual Analogue Scale (VAS-A). [At 12 months follow-up after treatment termination.]

    To what extend I feel anxious about flying by plane? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

Secondary Outcome Measures

  1. Anxiety. Administering a Visual Analogue Scale (VAS-A). [Before each exposure session.]

    To what extend I feel anxious now? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  2. Anxiety. Administering a Visual Analogue Scale (VAS-A). [Every 2 minutes during each exposure session of 60 minutes.]

    To what extend I feel anxious now? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  3. Anxiety. Administering a Visual Analogue Scale (VAS-A). [After eight sessions of treatment during eight weeks.]

    To what extend I feel anxious now? measured from 0 (absence of anxiety) to 10 (extreme anxiety).

  4. Sense of Presence. Administering the Visual Analogue Scale (VAS-P). [Every 2 minutes during each exposure session of 60 minutes.]

    To what extend I feel present now? measured from 0 (absence of sense of presence) to 10 (extreme sense of presence).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects who meet the Diagnostic and Statistical Manual of Mental Disorders (DSM-5, American Psychiatric Association, APA, 2013) criteria for FoF.
Exclusion Criteria:
  • Individuals with a diagnosis of panic disorder, obsessive-compulsive disorder, or psychotic disorder who have received psychotherapy for their FoF, have been taking prescribed medication for their FoF, or have experienced cardiorespiratory disease or an epilepsy attack will be excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Psychology. Universitat de Barcelona Barcelona Spain 08035

Sponsors and Collaborators

  • University of Barcelona

Investigators

  • Study Director: José MR Gutiérrez Maldonado, PhD, Senior PhD Supervisor

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
José María Ribé Viñes, Principal Investigator, University of Barcelona
ClinicalTrials.gov Identifier:
NCT05939986
Other Study ID Numbers:
  • 2926863
First Posted:
Jul 11, 2023
Last Update Posted:
Jul 11, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by José María Ribé Viñes, Principal Investigator, University of Barcelona

Study Results

No Results Posted as of Jul 11, 2023