Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06570603

Targeting Components of Distress Tolerance

Led by University of Arkansas, Fayetteville · Updated on 2025-07-10

240

Participants Needed

1

Research Sites

130 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn which aspects of distress intolerance (i.e., difficulties withstanding upsetting emotional states) are the most important for improving effective emotion regulation and associated mental health symptoms. The main questions it aims to answer are: How are willingness to feel upset and self-efficacy for withstanding distress associated with different emotion regulation strategies used in daily life? Does targeting willingness to feel upset and/or self-efficacy for withstanding distress help people use more effective emotion regulation strategies in daily life when they feel upset? Are improvements in emotion regulation strategies in daily life associated with fewer symptoms of mental health problems over time? Participants will: Answer questions about their moods, willingness to feel upset, self-efficacy for withstanding distress and emotion regulation strategies for three weeks using a cell phone app Undergo a willingness, self-efficacy, combined or psychoeducational control intervention in the lab Be prompted to use the intervention skill via the cell phone app during the second week, after the intervention Complete weekly reports of mental health symptoms

CONDITIONS

Official Title

Targeting Components of Distress Tolerance

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Fluent in English
  • Uses Android or iPhone smartphone
  • Depression Anxiety and Stress Scale (DASS-21) scores of 42 and higher
  • Distress Intolerance Index (DII) scores of 3 or higher
Not Eligible

You will not qualify if you...

  • Work or School that does not allow consistent access to phone (or is unsafe)
  • No internet access for completing follow-up surveys

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Arkansas - Fayetteville

Fayetteville, Arkansas, United States, 72701

Actively Recruiting

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Research Team

J

Jennifer C Veilleux, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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