An online platform for self-management of sexual assault recovery

Un Meilleur Sommeil Pour Une Meilleure Résilience : Une Plateforme En Ligne Autogérée Pour Les Victimes D'agression Sexuelle

NA · Laval University · NCT05811897

This study is testing an online therapy program to see if it helps women who have experienced sexual assault manage symptoms like PTSD and depression on their own or with some help from a therapist.

Quick facts

PhaseNA
Study typeInterventional
Enrollment204 (estimated)
Ages18 Years and up
SexAll
SponsorLaval University (other)
Locations1 site (Québec, Quebec)
Trial IDNCT05811897 on ClinicalTrials.gov

What this trial studies

This project aims to evaluate the effectiveness of a self-managed online cognitive behavioral therapy (CBT) platform designed for women who have experienced sexual assault. Given the significant barriers to accessing traditional CBT, particularly for this vulnerable population, the study will explore whether an online approach can provide a safe and effective alternative for managing psychological symptoms such as PTSD, insomnia, and depression. Participants will engage with the platform either independently or with therapist assistance, allowing for flexibility in treatment. The study seeks to address the lack of empirical evidence supporting self-care approaches for sexual assault survivors.

Who should consider this trial

Good fit: Ideal candidates are women aged 18 and older who have experienced sexual assault after the age of 12 and exhibit symptoms of PTSD, depression, or insomnia.

Not a fit: Patients with bipolar or psychotic disorders, high suicidal risk, or those already receiving psychological intervention may not benefit from this study.

Why it matters

Potential benefit: If successful, this platform could provide accessible mental health support for women recovering from sexual assault, potentially improving their psychological well-being.

How similar studies have performed: While there is growing evidence supporting online CBT for anxiety and mood disorders, this specific approach for sexual assault survivors is relatively novel and untested.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Identify at least in part as a woman;
2. Be at least 18 years old;
3. Have experienced SA after the age of 12;
4. Read and speak French;
5. Have adequate Internet access; and f) Present with some post-traumatic stress symptoms (PCL-5 ≥ 10) AND at least mild depressive symptoms (PHQ-9 ≥ 5) AND/OR subclinical insomnia symptoms (ISI ≥ 8).

Exclusion Criteria :

1. Bipolar or psychotic disorder;
2. High suicidal risk, or any other condition requiring immediate intervention;
3. Already benefiting from a psychological intervention.

Where this trial is running

Québec, Quebec

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Post Traumatic Stress Disorder, Insomnia Disorder, Major Depressive Disorder, mental health, post-traumatic stress disorder, psychological distress, sleep

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.