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Behavioral Intervention
Online EmReg Training for Emotion Regulation
N/A
Recruiting
Led By Maria Kajankova, PhD
Research Sponsored by Icahn School of Medicine at Mount Sinai
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 15 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to find the best way to train clinicians to use an online program that helps people manage their emotions. It compares a brief training with a more comprehensive training that includes additional support. The goal is to see which method helps clinicians deliver the program more effectively.
Who is the study for?
This trial is for licensed psychologists, social workers, or mental health counselors with CBT training and experience treating people with TBI. They must be able to provide group treatment online, have at least 3 patients suitable for EmReg based on emotion regulation difficulties, and commit to study tasks. Those already trained in EmReg or unwilling to do telehealth are excluded.
What is being tested?
The trial tests two ways of training clinicians: Standard Training (a workshop) versus Extended Training (workshop plus bi-weekly consultations). The goal is to find the best method for teaching Online EmReg implementation and measure patient improvement using clinician-administered DERS.
What are the potential side effects?
Since this trial focuses on training methods rather than medical interventions, traditional side effects aren't applicable. However, participants may experience stress or time constraints due to study commitments like training sessions and data collection.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 15 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 15 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Performance Evaluation (via Role Plays)
Provider Self-Efficacy Scale Score
Secondary study objectives
Acceptability of Intervention Measure (AIM)
Difficulties in Emotion Regulation Scale (DERS)
Feasibility of Intervention Measure (FIM) Scale
+6 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Extended TrainingExperimental Treatment2 Interventions
Participants assigned to this arm will complete the same 3-hour training workshop on the intervention as Arm #1. After completing the training, participants will also be asked to implement the intervention into their routine clinical practice. However, participants in this group will be asked to attend bi-weekly consultation sessions with members of the study team for 3 months following training.
Group II: Standard TrainingActive Control1 Intervention
Participants assigned to this arm will complete a 3-hour training workshop on the intervention. After completing the training, participants will be asked to implement the intervention into their routine clinical practice.
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
Common treatments for Traumatic Brain Injury (TBI) include cognitive-behavioral therapy (CBT) and other emotion regulation interventions. These treatments work by helping patients develop strategies to manage cognitive and emotional challenges resulting from TBI.
CBT, for example, focuses on changing negative thought patterns and behaviors, which can improve emotional regulation and reduce symptoms of anxiety and depression. This is crucial for TBI patients as emotional dysregulation can significantly impact their quality of life and hinder recovery.
Training clinicians to effectively deliver these interventions, as studied in the Online EmReg trial, ensures that patients receive consistent and effective care, ultimately aiding in their rehabilitation and improving long-term outcomes.
Treatment for posttraumatic stress disorder in patients with a history of traumatic brain injury: A systematic review.Critical appraisal of systematic reviews of executive function treatments in TBI.
Treatment for posttraumatic stress disorder in patients with a history of traumatic brain injury: A systematic review.Critical appraisal of systematic reviews of executive function treatments in TBI.
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Who is running the clinical trial?
Icahn School of Medicine at Mount SinaiLead Sponsor
903 Previous Clinical Trials
541,717 Total Patients Enrolled
Maria Kajankova, PhDPrincipal InvestigatorIcahn School of Medicine at Mount Sinai
2 Previous Clinical Trials
902 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am trained and experienced in Cognitive Behavioral Therapy.I am currently treating 3 or more patients with brain injuries who have trouble managing emotions.I am not willing to participate in group treatments online.
Research Study Groups:
This trial has the following groups:- Group 1: Standard Training
- Group 2: Extended Training
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.
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