Implementing an online emotion regulation program for traumatic brain injury

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial evaluates the effectiveness of an online emotion regulation intervention for individuals with traumatic brain injury (TBI) by comparing two training strategies for clinicians: Standard Training and Extended Training. The study aims to determine which training method better equips clinicians to deliver the Online EmReg intervention effectively. It employs a randomized design to assess both the implementation strategy and the clinical outcomes for patients receiving treatment. Clinician-administered assessments will measure patient improvements in emotion regulation.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Licensed psychologist, social worker, or mental health counselor.
* Training and experience in CBT, the framework for EmReg.
* Experience working with people with TBI.
* Experience providing group treatment.
* A computer and internet to conduct group treatment via telehealth.
* Actively treating ≥3 patients with TBI who are appropriate for EmReg (have emotion regulation difficulties based on clinician assessment).
* Amenable to study tasks (e.g., completion of training, consultation, performance based role-play, data collection).
* Not previously trained in EmReg.
* Proficient in English.

Exclusion Criteria:

* Not willing to conduct group treatment via telehealth.
* Non-English speaking.

Where it's running

• Icahn School of Medicine at Mount Sinai
  New York, New York, United States Recruiting

Study contacts

• Principal investigator: Maria Kajankova, PhD — Icahn School of Medicine at Mount Sinai
• Study coordinator: Emily Blunt, BA
• Email: emily.blunt@mountsinai.org
• Phone: 212-241-0818

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.