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Clinical Trials/NCT05955898
NCT05955898
Completed
Not Applicable

The Development and Evaluation of a Single Session Intervention for Parent Distress Tolerance

University of Miami1 site in 1 country50 target enrollmentMay 17, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parents
Sponsor
University of Miami
Enrollment
50
Locations
1
Primary Endpoint
Change in Distress Tolerance Scale scores
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

The purpose of this study is to study different ways to help parents cope with strong emotions. The study team will be looking at how two different treatments help parents learn to manage strong emotions. These treatments are one session and are completed online, without a therapist, like an online training or class.

Registry
clinicaltrials.gov
Start Date
May 17, 2024
End Date
June 27, 2024
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jill May Ehrenreich

Professor, Associate Chair

University of Miami

Eligibility Criteria

Inclusion Criteria

  • Live in the United States.
  • Parent of a child aged 6-17 years old who has received at least one counseling or mental health treatment session from a provider in the last 6 months will be eligible to participate.
  • Parent is not currently receiving psychotherapy or counseling for a mental health concern (or received such in the past six months).
  • Parent reported poor distress tolerance (DT). Poor DT will be defined as a score of less than 54 on the Distress Tolerance Scale.
  • Due to language limitations of the primary researcher, parents will be eligible if they comfortably speak and read in English.
  • Parents must have a mobile device (e.g., laptop, tablet, smart phone, etc.) or desktop computer and internet access sufficient for the delivery of the study assessments and intervention online.

Exclusion Criteria

  • Failure to meet any of the inclusion criteria.

Outcomes

Primary Outcomes

Change in Distress Tolerance Scale scores

Time Frame: Baseline, up to three-week follow-up

The Distress Tolerance Scale is a 15-item self-report measure that measures the perceived capacity to tolerate distress from a multidimensional framework, including tolerance, appraisal, absorption, and regulation. Items are rated on a 1-5 Likert scale and then summed. Scores range from 15-75. Higher total scores indicate greater ability to tolerate distress.

Secondary Outcomes

  • Change in Overall Anxiety Severity and Impairment Scale (OASIS) scores(Baseline, up to three-week follow-up)
  • Change in Parental Acceptance and Action Questionnaire (PAAQ) scores(Baseline, up to three-week follow-up)
  • Change in Overall Depression Severity and Impairment Scale (ODSIS) scores(Baseline, up to three-week follow-up)

Study Sites (1)

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