Assessing Social Learning and Course Delivery Timing in Internet-delivered Cognitive Behaviour Therapy for Public Safety Personnel
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Tunneled Delivery, Personalized Delivery, Standard Resources, Enhanced Social Learning Resources.
- Who it may be relevant to
- Registry conditions: Depression, Anxiety, Stress Disorders, Post-Traumatic. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Randomized Factorial Trial of Internet-delivered Cognitive Behaviour Therapy for Public Safety Personnel: Examining the Impact of Content Delivery Method
Overview
This study is a randomized factorial trial designed to evaluate unguided (i.e., purely self-help), transdiagnostic internet delivered cognitive behaviour therapy tailored for public safety personnel with tunneled of personalized course delivery and with or without the incorporation of social learning resources.
Detailed description
Background---- Public Safety Personnel (PSP) are at an increased risk of developing mental disorders. PSP also face many barriers to accessing mental health services (e.g., stigma, location, time). The PSP Wellbeing Course is a transdiagnostic internet-delivered cognitive behaviour therapy (ICBT) course that has been specifically tailored to PSP. The effectiveness of the therapist-guided course and a self-guided course have both been supported. Consistent with the larger literature on self-guided ICBT, engagement with and outcomes of the self-guided PSP Wellbeing Course could be strengthened. Persuasive design describes using technology to influence human behaviour. The current study is designed to assess the impact of different timing options (i.e., tunneled vs. personalized) and increased social learning (i.e., standard versus enhanced social learning) on user experience, adherence, and outcomes in ICBT.
Methods--- Participants will be recruited via posts on the PSPNET social media platforms (i.e., Twitter and Facebook) and emails distributed by PSP organizations. Members of the PSPNET team will also reach out to contacts within PSP organizations to ask them to tell their colleagues about the proposed research. All interested participants will be directed to the study website (www.pspnet.ca) to complete an online screening questionnaire. As part of this questionnaire, they will be presented with a consent form explaining the screening. After consent is given, clients will be assessed for eligibility using an online screening questionnaire. The online screening questionnaire captures demographic information (e.g., sex, ethnicity, location), information about depression and other mental health issues, and background information (e.g., medical history, mental health history, symptoms).
After completing the questionnaires, participant responses will be reviewed by PSP staff for eligibility. Clients who are eligible will be randomized into one of four conditions. Participants who do not meet criteria, but are over the age of 18, will not be randomized and will instead be enrolled into the "treatment-as-usual" version of the course, which consists of a tunneled delivery and standard resources. Ineligible participants' data will not be included in analyses. Individuals under the age of 18 will not be eligible for any services.The two factors in the trial are:
Factor 1: Tunneled course delivery or personalized course delivery
Factor 2: Standard or enhanced social learning resources.
As this is a factorial trial with two factors, each client will be randomized to one of four conditions:
Condition 1: Tunneled Delivery and Standard Resources Condition 2: Tunneled Delivery and Enhanced Social Learning Resources Condition 3: Personalized Delivery and Standard Resources Condition 4: Personalized Delivery and Enhanced Social Learning Resources
Randomization will occur within 2 business-days of completion of the screening questionnaires.
All participants will receive the Self-Guided PSP Wellbeing Course, a transdiagnostic internet intervention. The program is an adaptation of a previous Australian course, the Wellbeing Course. The course involved 5 lessons that are typically completed over an 8 week period, though participants will have access to the course materials for up to 26 weeks. The content is focused on cognitive behavior therapy and relapse prevention. Materials are presented in a didactic (i.e., text-based with visual images) and case-enhanced learning format (i.e., educational stories demonstrate the application of skills). All participants are presented with worksheets at the end of each lesson that contain exercises that facilitate skill acquisition. Participants will be sent automatic emails reminding them to stay engaged with the lessons and to complete questionnaires. Participants will complete questionnaires at screening, 4 weeks, 8 weeks (post-treatment), and 20 weeks (post-treatment).
Interventions
- Behavioral Tunneled Delivery
Participants will be offered a pre-determined pathway to completing the 8-week course - Behavioral Personalized Delivery
Participants will be able to complete course modules at their own pace and in the order that most interests them. - Behavioral Standard Resources
Participants will receive the resources as typically included in the Self-Guided PSP Wellbeing Course. - Behavioral Enhanced Social Learning Resources
Participants will receive additional intervention content. - Behavioral Transdiagnostic Self-Guided ICBT
An ICBT course that is completed without the guidance of a therapist.
Primary outcome measures
- Generalized Anxiety Disorder 7-item (GAD-7) [Time frame: Screening, 4 weeks, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- Patient Health Questionnaire-9 (PHQ-9) [Time frame: Screening, 4 weeks, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- PTSD Checklist for the DSM-5 (PCL-5) [Time frame: Screening, 4 weeks, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- Engagement [Time frame: From date of enrollment to 26 weeks (post-treatment)]
Secondary outcome measures (6)
- Work and Social Adjustment Scale (WSAS) [Time frame: Screening, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- Brief Resilience Scale (BRS) [Time frame: Screening, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- Healthcare Use Questionnaire [Time frame: Screening, 8 weeks (post-treatment), and 20 weeks (post-treatment)]
- Case Story Questionnaire [Time frame: 8-weeks (post-treatment)]
- Treatment Satisfaction Questionnaire [Time frame: 8-weeks (post-treatment)]
- Digital Behavior Change Interventions Engagement Scale (DCBI) [Time frame: 8-weeks (post-treatment)]
Eligibility criteria
Inclusion criteria
- At least 18 years of age
- Current or former public safety personnel (or public safety personnel trainee)
- Residing in Canada at time of enrollment
- Has regular access to the internet
- Confirms intent to participate in study
Exclusion criteria
- Not 18 years of age or older
- Not a current or former public safety personnel (or public safety personnel trainee)
- Not residing in Canada at time of enrollment
- Does not have regular access to the internet
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Factorial
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Canada · 1 center
- Department of Psychology, University of Regina — Regina
Identifiers
NCT: NCT06298279 · 2023-436