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Clinical Trials/NCT03056963
NCT03056963
Completed
Not Applicable

Guided Imagery Training and Self-Referential Processing

University of Texas at Austin1 site in 1 country86 target enrollmentMarch 17, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
University of Texas at Austin
Enrollment
86
Locations
1
Primary Endpoint
Change in response on the Self-Referent Encoding Task (SRET)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to examine the efficacy of a guided imagery paradigm for reducing negative ways of thinking about the self. There will be at least 60 participants enrolled at the University of Texas at Austin. Participants will be randomly selected to receive one of two types of trainings, each over the course of two weeks. Participants will undergo the training exercises at home. The training exercises will help them to think differently about themselves.

Participants will be able to determine if they are eligible, and then participate, by filling out a screening questionnaire online.

Detailed Description

This study uses a randomized controlled trial to compare two types of guided imagery. One intervention is an active intervention; the other is intended to be inert. These interventions were developed based on extensive research indicating the efficacy of using imagery in depression, and a perceived lack of treatments targeting biased self-referential processing. This protocol aims to develop a novel intervention which can be used on its own or as an adjunct to existing treatments. Common treatments for Major Depressive Disorder (MDD) are diffuse; this paradigm instead aims to specifically target negative self-schema, a part of the cognitive model of MDD. This study focuses on participants with elevated depressive symptoms.

Registry
clinicaltrials.gov
Start Date
March 17, 2017
End Date
June 19, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • willing and able to provide informed consent
  • elevated depressive symptoms -- i.e., a score above a 13 on the Center for Epidemiologic Studies Depression Scale (CESD)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in response on the Self-Referent Encoding Task (SRET)

Time Frame: Participants will complete the SRET at baseline, after one week, and after two weeks. Change will be assessed primarily as SRET at two weeks MINUS SRET at baseline.

The SRET is a task that asks participants to categorize words as self-referential or not. Its outcomes are focused on behavioral response and reaction time. We have shown that it has good test-retest reliability over the course of one week.

Secondary Outcomes

  • Depressive Symptomatology(Participants will complete measures of depressive symptoms at baseline, after one week, and after two weeks.)

Study Sites (1)

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