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Clinical Trials/NCT04584879
NCT04584879
Completed
N/A

Transdiagnostic Treatment Personalization: Prioritizing Therapy Components to Capitalize on Strengths or Compensate for Weaknesses

Shannon E. Sauer-Zavala1 site in 1 country72 target enrollmentOctober 28, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anxiety Disorders
Sponsor
Shannon E. Sauer-Zavala
Enrollment
72
Locations
1
Primary Endpoint
Change in Clinical Severity
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The primary purpose of this study is to explore whether the efficiency of treatment for anxiety and depressive disorders can be increased using two discrete strategies: personalized skill ordering and 2) treatment discontinuation based on proximal indicators of improvements. The present study will specifically use treatment components drawn from an evidence-based psychological intervention, the Unified Protocol for the Transdiagnostic Treatment of Emotional Disorders (UP). This intervention has strong empirical support for patients presenting with anxiety, depressive, and related disorders and contains therapeutic skills that are common in psychological interventions (e.g., psychoeducation, mindfulness training, cognitive restructuring, countering emotional avoidance, increasing interoceptive tolerance). This study will determine if prioritizing the order of treatment modules to capitalize on patient strengths or compensate for weakensses increases treatmen efficacy. Additionally, it will also identify under what conditions briefer treatment modules may be appropriate.

Registry
clinicaltrials.gov
Start Date
October 28, 2019
End Date
September 15, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shannon E. Sauer-Zavala
Responsible Party
Sponsor Investigator
Principal Investigator

Shannon E. Sauer-Zavala

Assistant Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • diagnosis of at least one emotional disorder
  • fluent in English
  • medication stability

Exclusion Criteria

  • concurrent therapy
  • psychological condition that would be better addressed by alternative treatments
  • have received more than 5 sessions of cognitive behavioral therapy in the past 5 years

Outcomes

Primary Outcomes

Change in Clinical Severity

Time Frame: 12 weeks (baseline, week 6 and week 12)

Clinical severity will be measured using the Diagnostic Interview for Anxiety, Mood, and Obsessive Compulsive and Related Neuropsychiatric Disorders (DIAMOND) dimensional clinician ratings. Scores range from 1-7; higher scores indicate greater severity.

Change in Anxiety Symptoms

Time Frame: 12 weeks (baseline, week 1, week, 2, week, 3.....week 12)

Anxiety symptoms will be measured using the Overall Anxiety Severity and Interference Scale (OASIS). This is a self-report measure in which scores range from 0-20; higher scores indicate more severe anxiety symptoms.

Change in Depressive Symptoms

Time Frame: 12 weeks (baseline, week 1, week, 2, week, 3.....week 12)

Depressive symptoms will be measured using the Overall Depression Severity and Interference Scale (ODSIS). This is a self-report measure in which scores range from 0-20; higher scores indicate more severe anxiety symptoms.

Change in Aversive Reactions to Emotions

Time Frame: 12 weeks (baseline, week 1, week, 2, week, 3.....week 12)

Aversive reactions to emotions will be measured using the distress aversion subscale of the Multidimensional Experiential Avoidance Questionnaire (MEAQ). This is a self-report measure in which scores range from 13-78; higher scores indicate greater negative reactions to emotional experiences.

Study Sites (1)

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