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Combined CBT and DBT Skills Group for High-Risk Psychosis
N/A
Recruiting
Led By Leslie Horton, PhD
Research Sponsored by University of Pittsburgh
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
13-18 years of age
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 4 months vs up to 7 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a new group therapy combining CBT and DBT for teens at high risk of psychosis. The therapy includes regular sessions to help manage stress, think more flexibly, and improve social skills. The goal is to see if this approach can improve mental health and functioning in these young people.
Who is the study for?
This trial is for adolescents and young adults aged 13-18 who are at clinical high-risk (CHR) for psychosis. Participants must be receiving services from the HOPE team at the University of Pittsburgh and meet specific criteria indicating a risk for developing a psychotic disorder, such as having certain symptoms or family history.
What is being tested?
The study tests an integrated skills group that combines cognitive behavioral therapy (CBT) and dialectical behavioral therapy (DBT). It's designed to help those at CHR manage their symptoms. The feasibility and outcomes of this weekly group will be evaluated over approximately 6-7 months.
What are the potential side effects?
Since this intervention involves psychological therapies rather than medications, traditional side effects are not expected. However, participants may experience emotional discomfort or distress while discussing personal issues during sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 13 and 18 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 4 months vs up to 7 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 4 months vs up to 7 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Attendance
Attrition
Change from 4 months in Satisfaction with Therapy and Therapist Scale at up to 7 months
+10 moreSecondary study objectives
Change from baseline Child and Adolescent Mindfulness Measure at up to 4 months
Change from baseline Child and Adolescent Mindfulness Measure at up to 7 months
Change from baseline Overcontrol/uncontrol word pairs at up to 4 months
+50 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Skills GroupExperimental Treatment1 Intervention
There will be one condition which is the group and participants will complete feasibility and outcome measures at baseline (within 1 month), at midpoint (3-4 months after baseline), and at the end of the group (6-7 months after baseline).
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cognitive Behavioral Therapy (CBT) and Dialectical Behavior Therapy (DBT) are common treatments for mental health that work by addressing negative thought patterns and behaviors. CBT helps patients identify and change these patterns to improve emotional regulation and reduce symptoms.
DBT, an adaptation of CBT, adds mindfulness and stress tolerance techniques to manage intense emotions and reduce self-destructive behaviors. These therapies are crucial for mental health patients, especially those at high risk for psychosis, as they provide practical skills for coping with distress, improving emotional regulation, and enhancing interpersonal effectiveness.
Acute and one-year outcome of a randomised controlled trial of brief cognitive therapy for major depressive disorder in primary care.Problem-Focused Psychodynamic Psychotherapies.A randomised trial of dialectical behaviour therapy and the conversational model for the treatment of borderline personality disorder with recent suicidal and/or non-suicidal self-injury: An effectiveness study in an Australian public mental health service.
Acute and one-year outcome of a randomised controlled trial of brief cognitive therapy for major depressive disorder in primary care.Problem-Focused Psychodynamic Psychotherapies.A randomised trial of dialectical behaviour therapy and the conversational model for the treatment of borderline personality disorder with recent suicidal and/or non-suicidal self-injury: An effectiveness study in an Australian public mental health service.
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Who is running the clinical trial?
University of PittsburghLead Sponsor
1,787 Previous Clinical Trials
16,359,323 Total Patients Enrolled
2 Trials studying Mental Health
1,469 Patients Enrolled for Mental Health
Substance Abuse and Mental Health Services Administration (SAMHSA)FED
30 Previous Clinical Trials
23,236 Total Patients Enrolled
Leslie Horton, PhDPrincipal InvestigatorUniversity of Pittsburgh
1 Previous Clinical Trials
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am at high risk for developing a psychotic disorder.I am between 13 and 18 years old.My child is at risk for developing psychosis.
Research Study Groups:
This trial has the following groups:- Group 1: Skills Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Mental Health Patient Testimony for trial: Trial Name: NCT05398120 — N/A
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