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A Randomized Controlled Trial of Brief Interventions for Coping with Distress
This study is being done to compare the effectiveness of three different skills trainings to cope with distress. These three trainings are: 1) an attention skills training, 2) an attention and reflective thought skills training, and 3) a health and wellness education training.
Adults living in New York City between the ages of 18-65 and experiencing elevated levels of worry, rumination, and/or self-criticism may be eligible to participate. After being informed about the study and potential risks, participants giving written informed consent will complete an online screening visit to determine full study eligibility. Eligible participant will then be randomized to complete 6-weeks of one of three self-directed, online skills training about coping with distress. The present study is evaluating whether these skills trainings demonstrate efficacy in: 1) improving outcomes specific to an emotion regulation model of emotional distress (e.g., attentional control, decentering, reappraisal); 2) reducing symptoms of psychological distress (e.g., anxiety, depression, worry, rumination). Primary assessment points will take place before and after the skills training, and will include self-report measures, brief surveys during daily life, as well as computer tasks and measures of brain and body activity (e.g., EEG).
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Teachers College, Columbia University
New York, New York, United States
Start Date
May 12, 2023
Primary Completion Date
December 1, 2025
Completion Date
December 1, 2025
Last Updated
November 21, 2024
180
ESTIMATED participants
Online, Self-Directed Attention Skills Training with Coaching Support
BEHAVIORAL
Online, Self-Directed Attention & Reflective Thought Skills Training with Coaching Support
BEHAVIORAL
Online, Self-Directed Health & Wellness Education Training with Coaching Support
BEHAVIORAL
Lead Sponsor
Teachers College, Columbia University
NCT07478393
NCT07456631
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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