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Grant: Project Grant

Université du Québec à Montréal

$325,124.00

Assessing the Effectiveness of Virtual Reality Exposure Therapy for Sexual Aversion Disorder: A Multisite Randomized Controlled Trial

FY 2024-25

Summary
BACKGROUND: Sexual Aversion Disorder (SAD) affects 1 in 10 adults and is characterized by fear, disgust, and avoidance of sexual contexts. The most effective treatment for SAD is exposure-based sex therapy, which involves graded and repeated exposure to fear- and disgust-eliciting sexual situations. Yet, access to such treatments remains limited in Canada, leaving many without adequate care. One-session Virtual Reality Exposure Therapy (VRET) is a time-efficient treatment that immerses individuals in digital scenarios mimicking real-life situations, offering a promising approach for SAD patients to safely confront and process feared sexual contexts. Our team developed and pilot-tested a one-session VRET for SAD, demonstrating its potential as an effective, acceptable, and safe treatment. PRIMARY AIM: To assess the effectiveness of one-session VRET for SAD in reducing (1) sexual fear, (2) sexual disgust, and (3) sexual avoidance. RESEARCH PLAN: This clinical trial will randomly assign 208 adults with SAD to either a group that will receive one-session VRET (EXP) or a waitlist control group (CTL). VRET effectiveness will be assessed by comparing participants' SAD symptoms at baseline (T1) with their levels at one week (T2), three months (T3), and six months (T4) post-treatment, and by measuring symptom differences between the EXP and CTL groups. VRET includes interventionist-guided exposure to 15 VR scenarios that progressively increase in sexual explicitness. OUTCOMES: EXP and CTL groups will complete validated measures of sexual fear, disgust, and avoidance at T1, T2, T3, and T4, with the CTL group being offered VRET after completing T3. IMPLICATIONS: If effective, this VRET will provide an innovative, time-efficient, and scalable treatment for Canadians with SAD, facilitating its clinical implementation through diverse knowledge mobilization efforts, clinical partnerships, and open-access availability of the VRET application.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
522131
Name
Lafortune David
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Psychosocial, Sociocultural & Behavioural Determinants of Health
Projecttitle
Assessing the Effectiveness of Virtual Reality Exposure Therapy for Sexual Aversion Disorder: A Multisite Randomized Controlled Trial
Programtype2
Operating Grants
Orgnameinp2
Université du Québec à Montréal
Cihramount2
$325,124
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Exposure Therapy; Randomized Controlled Trial; Sex Therapy; Sexual Aversion Disorder; Sexual Dysfunctions; Treatment Effectiveness; Virtual Reality
Abstract
BACKGROUND: Sexual Aversion Disorder (SAD) affects 1 in 10 adults and is characterized by fear, disgust, and avoidance of sexual contexts. The most effective treatment for SAD is exposure-based sex therapy, which involves graded and repeated exposure to fear- and disgust-eliciting sexual situations. Yet, access to such treatments remains limited in Canada, leaving many without adequate care. One-session Virtual Reality Exposure Therapy (VRET) is a time-efficient treatment that immerses individuals in digital scenarios mimicking real-life situations, offering a promising approach for SAD patients to safely confront and process feared sexual contexts. Our team developed and pilot-tested a one-session VRET for SAD, demonstrating its potential as an effective, acceptable, and safe treatment. PRIMARY AIM: To assess the effectiveness of one-session VRET for SAD in reducing (1) sexual fear, (2) sexual disgust, and (3) sexual avoidance. RESEARCH PLAN: This clinical trial will randomly assign 208 adults with SAD to either a group that will receive one-session VRET (EXP) or a waitlist control group (CTL). VRET effectiveness will be assessed by comparing participants' SAD symptoms at baseline (T1) with their levels at one week (T2), three months (T3), and six months (T4) post-treatment, and by measuring symptom differences between the EXP and CTL groups. VRET includes interventionist-guided exposure to 15 VR scenarios that progressively increase in sexual explicitness. OUTCOMES: EXP and CTL groups will complete validated measures of sexual fear, disgust, and avoidance at T1, T2, T3, and T4, with the CTL group being offered VRET after completing T3. IMPLICATIONS: If effective, this VRET will provide an innovative, time-efficient, and scalable treatment for Canadians with SAD, facilitating its clinical implementation through diverse knowledge mobilization efforts, clinical partnerships, and open-access availability of the VRET application.
Competitiondate
202503
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Lafortune, David; Brotto, Lori Anne
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $325,124~ $0~
Université du Québec à Montréal - $325,124 Grant (202… | Canada Spends