Efficacy of a Gamified Augmented Reality Exposure-based Application in Subjects With Fear of Spiders

Prof. Dominique de Quervain, MD60 enrolled

Overview

Investigation of the efficacy of a gamified augmented reality exposure app in individual with fear of spiders.

The study will be conducted as a randomized controlled between subject trial. The study consists of two visits and a home training for one group. 60 participants between 18 and 40 years with clinical or subclinical fear of spiders will take part in the study. All assessments of outcome will be conducted on one visit for each participant, including an in vivo BAT. The experimental group will participate in a home training with the app, spanning over two weeks (6x30-minutes sessions), whereas the control group will not receive any treatment (untreated comparison group). Six weeks after the first visit all participants undergo the assessments of outcome, including a second in vivo BAT. The BAT will take place 4 weeks after completion of the home training. This design allows a direct comparison and therefore an estimation of the efficacy of the gamified AR exposure therapy.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

SINGLE

Enrollment

Conditions

Fear of Spiders

Interventions

AR appOTHER

Participants will be exposed to nine different AR spider scenarios with a pre-defined length of 2 minutes for each level. Each level starts with a surface scan of the environment and the placement of the AR spider model(s) by tapping on the display. Through small text pop-ups the user is instructed to perform different tasks (e.g. looking at the spider model, approaching it, holding the hand under the model). They proceed to further levels according to a predefined exposure scheme based on SUDS for fear (scale 0=no fear to 10=maximum fear) and disgust (scale 0=no disgust to 10=maximum disgust) and the assurance of the task completed (yes/no). Users will repeat each level until their SUDS are 4 or below and have completed the task. Each exposure session is limited to approx. 30 minutes (controlled by the participants) irrespective of achieved level.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 40 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Fear of spiders * BAT score before exposure between 1-8 * Physically healthy * Fluent in German Exclusion Criteria: * BDI-II sumscore \>=20 and/or item 9 \>=1 * Concurrent psychotherapy or pharmacotherapy * Previous exposure-based therapy for spider phobia * Parallel participation in another study * Chronic medication intake (except oral contraceptives) * Medication intake before visits (less than 24h) * Alcohol intake before visits (less than 12 h) * Cannabis or other psychoactive substances (including benzodiazepines) intake before visits (less than 5 days) * For women: Current pregnancy

Locations (1)

University of Basel

Basel, Canton of Basel-City, Switzerland

Outcomes

Primary Outcomes

Subjective fear (SUDS) in the in vivo BAT

During the BAT participants will be placed in front of a closed room with a spider in it and will be asked to open the door and approach a living house spider measuring about 5 cm, which will be placed in a sealed transparent plastic container on a table at the far end of the room. The participant will be requested to approach the spider and if possible, to touch the container, to remove the lid, insert a hand, and try to pick up and hold the spider for at least 20 s. Pre-defined scores ranging from 0 = refuses to enter the test room to 12 = holds the spider for at least 20 s will be given when the BAT was completed after 3 minutes or terminated by the participant. SUDS for fear and disgust will be taken during the BAT on the same score as on day one, ranging from 0 = no fear to 10 = maximum fear.

Time frame: 6 weeks after day one (4 weeks after completion of home training)

Secondary Outcomes

Performance Behavioural Approach Test (BAT) in vivo

See primary outcome for a detailed description.

Time frame: 6 weeks after day one (4 weeks after completion of home training)

Subjective disgust (SUDS) in the in vivo BAT

See primary outcome for a detailed description.

Time frame: 6 weeks after day one (4 weeks after completion of home training)

Fear of spiders Questionnaire (FSQ)

The FSQ measures avoidance behavior as well as fear of harm and consists of 18 spider relevant situations. Participants evaluate their relationship to spiders on a 7-point Likert-type scale (0 = not at all true to 6 = absolutely true, range 0 - 108) (Szymanski and O'Donohue, 1995)

Time frame: 6 weeks after day one (4 weeks after completion of home training)

Spider Beliefs Questionnaire (SBQ)

The SBQ assesses specifically spider-related catastrophic cognitions that will be challenged within the exposure sessions and consists of 48 possible thoughts and beliefs in spider situations. Participants evaluate whether they are convinced these beliefs are true while being in a spider situation with a percentage (0 = not at all convinced to 100 = firmly convinced) (Arntz et al. 1993)

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.