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临床试验/NCT04584879
NCT04584879已完成不适用

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

Shannon E. Sauer-Zavala1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2019年10月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
72
试验地点
1
主要终点
Change in Clinical Severity

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

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

排除标准

  • •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

研究组 & 干预措施

Standard Group, Brief Intervention

Experimental

Participants in this group will receive 6 sessions of treatment in accordance with the standard, published Unified Protocol (UP) manual.

干预措施: Standard UP Treatment (Behavioral)

Standard Group, Full Intervention

Experimental

Participants in this group will receive 12 sessions of treatment in accordance with the standard, published Unified Protocol (UP) manual.

干预措施: Standard UP Treatment (Behavioral)

Capitalization Group, Brief Intervention

Experimental

Participants in this group will receive 6 sessions of treatment organized to prioritize skills that capitalize on patient strengths.

干预措施: Capitalization UP Treatment (Behavioral)

Capitalization Group, Full Intervention

Experimental

Participants in this group will receive 12 sessions of treatment organized to prioritize skills that capitalize on patient strengths.

干预措施: Capitalization UP Treatment (Behavioral)

Compensation Group, Brief Intervention

Experimental

Participants in this group will receive 6 sessions of treatment organized to prioritize skills that compensate for patient weaknesses.

干预措施: Compensation UP Treatment (Behavioral)

Compensation Group, Full Intervention

Experimental

Participants in this group will receive 12 sessions of treatment organized to prioritize skills that compensate for patient weaknesses.

干预措施: Compensation UP Treatment (Behavioral)

结局指标

主要结局

Change in Clinical Severity

时间窗: 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

时间窗: 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

时间窗: 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

时间窗: 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.

次要结局

未报告次要终点

研究者

发起方
Shannon E. Sauer-Zavala
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Shannon E. Sauer-Zavala

Assistant Professor

University of Kentucky

研究点 (1)

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