- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05100875
Social Skills and Emotion Regulation Training "SSERT" for Trauma in Psychosis (SSERT)
August 26, 2024 updated by: Martin Lepage, Douglas Mental Health University Institute
Social Skills and Emotion Regulation Training "SSERT" for Trauma in Psychosis: A Pilot Feasibility and Acceptability Study
This study will investigate if the SSERT (Social Skills and Emotion Regulation Training) intervention is feasible and acceptable in individual with psychotic disorder and a history of trauma.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Many individuals with psychotic disorders experience poor functional outcomes such as lower quality of life, lower levels of education, and lower life expectancy.
Comorbid mental disorders, such as posttraumatic stress disorder and related posttraumatic stress symptoms tend to aggravate psychotic symptoms and, as a result, worsen functional outcomes.
Further, emotion regulation and interpersonal functioning are generally impaired in individuals with psychotic disorders and histories of childhood trauma, and preliminary evidence suggests that these impairments may mediate the relationship between childhood trauma and psychotic symptom severity.
Despite the high levels of trauma observed in psychotic populations, the last decade has seen only a modest increase in the number of trials examining the efficacy of trauma interventions in this population.
Further, given the initial distress, destabilization, and increased vulnerability that may occur when first engaging in trauma-focused intervention, it has been argued that in those with psychotic disorders, stabilizing/grounding interventions may be a necessary fist step prior to engagement in trauma therapy.
This study will thus assess whether the Social Skills and Emotion Regulation Training (SSERT) for Trauma in Psychosis is feasible and acceptable to offer as a preparatory intervention, and will examine its preliminary effect on emotion regulation, interpersonal functioning, and other functional outcomes.
SSERT proposes a single-arm baseline with post-intervention design.
We will recruit 20 participants with a psychotic disorder, a history of trauma, and an impairment in interpersonal functioning and/or emotion regulation.
The intervention will consist of nine weekly hour-long individual sessions and one final 90-minute session.
The feasibility of SSERT will be assessed by examining the profile or safety of the study (including whether there are any adverse events reported), the participant flow (missed sessions, attrition rates, retention/completion rates), and through both standardized and qualitative items assessing therapist feedback.
The acceptability of SSERT will be assessed subjectively, specifically though participant responses on therapy satisfaction, therapeutic alliance, and motivation for therapy questionnaires.
Qualitative analyses will identify common themes and assess participant comments.
We expect that SSERT will be both feasible and acceptable to administer to this population.
Any expectations regarding the intervention's effect in improving emotion regulation, interpersonal functioning, and other functional outcomes is exploratory.
Overall, SSERT may help people with psychotic disorders to better understand how the experience and effect of trauma impacts their relationships and emotion management.
The intervention may also help to improve functional outcomes and relationship quality by teaching emotion regulation and grounding strategies, and through learning to become more engaged and flexible in relationships.
Study Type
Interventional
Enrollment (Actual)
19
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Quebec
-
Verdun, Quebec, Canada, H4H 1R3
- Douglas Research Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- (1) diagnosis of a schizophrenia spectrum or other psychotic disorder including affective psychosis;
- (2) trauma history meeting Diagnostic and Statistical Manual of Mental Disorders (DSM-5) PTSD criterion A;
- (3) at least a mild impairment in either emotional regulation or interpersonal functioning, identified using predetermined cut-offs of ≤ 2 on the Emotion Regulation Skills Questionnaire or ≥ 1 on the Inventory or Interpersonal Problems-32 ;
- (4) at least 18 years of age;
- (5) clinically stable/taking a stable dose of antipsychotic medication;
- (6) French or English-speaking; and
- (7) with no major physical illness.
Exclusion Criteria:
- (1) history of a medical or neurological condition that can affect cognition, which will be verified via participant self-report;
- (2) current severe substance use disorder; and
- (3) an IQ score below 70, estimated using the Wechsler Abbreviated Scale of Intelligence - Two subtest version (vocabulary, matrix reasoning)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention SSERT
The SSERT intervention will take place over 10 weekly individual intervention sessions of 60 minutes.
SSERT for trauma history in psychosis will draw inspiration from the Skills Training in Affective and Interpersonal Regulation intervention as well as other CBT and DBT-based interventions for emotion regulation and social skills functioning.
Therapists will be provided with a semi-structured manual that can be implemented flexibly to consider participant needs.
|
The SSERT intervention will broadly consist of the following 10 modules: (1) Introducing the Participant to Treatment; (2-3) Emotional Awareness and Recognition; (4-5) Emotion Regulation and Understanding Emotions in the Context of Psychotic Experiences; (6) Living an Emotionally Engaged Life; (7) Understanding Relationship Patterns in the Context of Psychosis; (8) Changing Undesirable Relationship Patterns; (9) Learning to have agency in Relationships; and (10) Flexibility in Relationships and Transitioning to Trauma-Focused Therapy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participant completion rate
Time Frame: 10 weeks of the intervention
|
Feasibility, percentage of participants to complete at least 50% of sessions
|
10 weeks of the intervention
|
|
Adverse events
Time Frame: 10 weeks of the intervention
|
Feasibility, number of recorded adverse events directly associated with the trial
|
10 weeks of the intervention
|
|
SSERT Feasibility Questionnaire-Therapist
Time Frame: Completion time 10 minutes
|
Feasibility, self-report questionnaire completed by the therapist
|
Completion time 10 minutes
|
|
Working Alliance Inventory-Short Revised
Time Frame: Completion time 5 minutes
|
Acceptability, self-report questionnaire
|
Completion time 5 minutes
|
|
Client Motivation for Therapy Scale
Time Frame: Completion time 5 minutes
|
Acceptability, self-report questionnaire
|
Completion time 5 minutes
|
|
Client Satisfaction Questionnaire
Time Frame: Completion time 5 minutes
|
Acceptability/satisfaction, self-report questionnaire
|
Completion time 5 minutes
|
|
The Satisfaction with Therapy Questionnaire
Time Frame: Completion time 5 minutes
|
Acceptability/satisfaction, self-report questionnaire
|
Completion time 5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emotion Regulation Skills Questionnaire
Time Frame: Completion time 5 minutes
|
Emotion regulation, self-report questionnaire
|
Completion time 5 minutes
|
|
Inventory of Interpersonal Problems- 32
Time Frame: Completion time 5 minutes
|
Interpersonal functioning, self-report questionnaire
|
Completion time 5 minutes
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The PTSD Checklist for DSM-5
Time Frame: Completion time 10 minutes
|
Posttraumatic stress symptoms, self-report questionnaire
|
Completion time 10 minutes
|
|
The Dissociative Experiences Scale II
Time Frame: Completion time 10 minutes
|
Dissociative symptoms, self-report questionnaire
|
Completion time 10 minutes
|
|
Positive and Negative Syndrome Scale-6 (PANSS-6)
Time Frame: Evaluation time 20 minutes
|
Psychotic symptoms, observer-rated measure
|
Evaluation time 20 minutes
|
|
Psychotic Symptoms Rating Scales, distress dimension
Time Frame: Evaluation time 10 minutes
|
Distress associated with psychotic symptoms, observer-rated measure
|
Evaluation time 10 minutes
|
|
Beck Cognitive Insight Scale
Time Frame: Completion time 5 minutes
|
Metacognition, self-report questionnaire
|
Completion time 5 minutes
|
|
Overall Anxiety and Severity Impairment Scale
Time Frame: Completion time 5 minutes
|
Anxiety, self-report questionnaire
|
Completion time 5 minutes
|
|
Patient Health Questionnaire-9
Time Frame: Completion time 5 minutes
|
Depression, self-report questionnaire
|
Completion time 5 minutes
|
|
Brief COPE scale
Time Frame: Completion time 5 minutes
|
Coping, self-report questionnaire
|
Completion time 5 minutes
|
|
Abbreviated- Quality of Life Enjoyment and Satisfaction Questionnaire
Time Frame: Completion time 5 minutes
|
Quality of life, self-report questionnaire
|
Completion time 5 minutes
|
|
Self-Esteem Rating Scale- Short Form
Time Frame: Completion time 5 minutes
|
Self-esteem, self-report questionnaire
|
Completion time 5 minutes
|
|
The Warwick-Edinburgh Mental Well-being Scale
Time Frame: Completion time 5 minutes
|
Wellbeing, self-report questionnaire
|
Completion time 5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2021
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
March 31, 2024
Study Registration Dates
First Submitted
July 26, 2021
First Submitted That Met QC Criteria
October 20, 2021
First Posted (Actual)
October 29, 2021
Study Record Updates
Last Update Posted (Actual)
August 27, 2024
Last Update Submitted That Met QC Criteria
August 26, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SSERT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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