Emotion Regulation Training Via Telehealth During the COVID-19 Pandemic
Purpose
This study is an open trial designed specifically to address the need for evidence-based treatment delivered via telehealth to individuals that are currently struggling with mental health issues during the COVID-19 pandemic, with the overarching goal of helping residents of New York adversely impacted by the pandemic to effectively manage their anxiety, stress, and depression during this unprecedented time in human history.
Conditions
- Distress, Emotional
- Emotional Dysfunction
- Anxiety
- Depression
Eligibility
- Eligible Ages
- Between 18 Years and 65 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Aged 18-65 years during the time of participation - Endorses distress and worry/rumination exacerbated by the COVID-19 pandemic - Access to a mobile device (e.g., smartphone, personal computer, laptop, tablet) connected to the Internet
Exclusion Criteria
- Active suicidal intent - Current substance dependence disorder (within the past year) - Current or past psychotic disorder, Bipolar-I disorder, or dementia - Primary DSM-5 diagnosis of borderline or narcissistic personality disorder - Currently receiving any other form of psychosocial treatment
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Intervention Model Description
- All participants will receive a 9-session version of Emotion Regulation Training delivered semi-weekly via synchronous telehealth using videoconferencing software and an asynchronous Internet-based Online platform to supplement the content covered in each session.
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Emotion Regulation Training via Telehealth |
All participants will receive 9 sessions of Emotion Regulation Training delivered via telehealth. These individualized therapy sessions are 1-hour in length and occur semi-weekly over the course of four weeks. |
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Recruiting Locations
More Details
- NCT ID
- NCT04615416
- Status
- Active, not recruiting
- Sponsor
- Teachers College, Columbia University
Detailed Description
The present study is evaluating whether this ERT treatment program delivered via telehealth demonstrates efficacy in: 1) reducing symptoms of psychological distress (e.g., anxiety, depression, worry, rumination); 2) improving outcomes specific to the ERT mechanism-based model (e.g., attentional control, decentering, reappraisal); 3) improving quality of life and functioning, for adults aged 18-65 years old.