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Enhancing Exposure Therapy for Snake and Spider Phobias (Snake/Spider)

Primary Purpose

Specific Phobia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Exposure Therapy with Retrieval
Exposure Therapy with Compound Extinction
Exposure Therapy with Retrieval and Compound Extinction
Therapist-guided Exposure Therapy
Sponsored by
University of Texas at Austin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Specific Phobia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age 18 to 65.
  2. Speaks English fluently.
  3. A score of 70 or higher on the Fear of Snakes/Spiders Questionnaire.
  4. Demonstrates avoidance during behavioral approach tests (defined as inability to put palm flat on the bottom of a tank containing a snake/spider, and inability to touch a snake/spider with a bare finger).

Exclusion Criteria:

  1. Unstable dose of psychotropic medications during the 4 weeks prior to baseline assessment.
  2. Currently receiving exposure-based treatment for snake/spider phobia.
  3. Currently at risk for suicide.

Sites / Locations

  • University of Texas at Austin

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Active Comparator

Arm Label

Exposure with Retrieval

Exposure with Compounding

Exposure with Retrieval and Compounding

Therapist-Guided Exposure Therapy

Arm Description

Exposure Therapy with Retrieval

Exposure Therapy with Compound Extinction

Exposure Therapy with Retrieval and Compound Extinction

Therapist-guided Exposure Therapy

Outcomes

Primary Outcome Measures

Change in peak subjective fear (0 - 100), behavioral approach (0 - 4), and heart rate reactivity to a live snake/spider not used during treatment (generalization context) from pre-treatment to follow-up

Secondary Outcome Measures

Change in peak subjective fear (0 - 100), behavioral approach (0 - 4), and heart rate reactivity to a live snake/spider not used during treatment (generalization context) from pre-treatment to post-treatment.
Change in peak subjective fear (0 - 100), behavioral approach (1 - 8), and heart rate reactivity to a live snake/spider used during treatment (treatment context) from pre-treatment to follow-up
Change in peak subjective fear (0 - 100), behavioral approach (1 - 8), and heart rate reactivity to a live snake/spider used during treatment (treatment context) from pre-treatment to post-treatment
Change in Fear of Snakes/Spiders Questionnaire from pre-treatment to follow-up
Change in Snake/Spider Belief Questionnaire from pre-treatment to follow-up
Change in Agoraphobic Cognitions Questionnaire for Snake/Spider Phobia from pre-treatment to follow-up
Change in Self-Efficacy Questionnaire for Spider/Snake Phobia from pre-treatment to follow-up
Change in Armfield and Mattiske Disgust Questionnaire from pre-treatment to follow-up
Change in Lab for the Study of Anxiety Disorders Specific Phobia Diagnostic Questionnaire from pre-treatment to follow-up
change from pre-treatment in current phobic diagnostic status and in level of phobic-related distress and impairment

Full Information

First Posted
January 22, 2014
Last Updated
December 4, 2020
Sponsor
University of Texas at Austin
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT02160470
Brief Title
Enhancing Exposure Therapy for Snake and Spider Phobias
Acronym
Snake/Spider
Official Title
Enhancing Exposure Therapy for Snake and Spider Phobias With Fear Retrieval and Compound Extinction
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
August 2012 (Actual)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas at Austin
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study tests whether exposure therapy for fear of snakes or spiders is enhanced by the addition of a brief fear retrieval trial prior to treatment, and the use of compound extinction during treatment. The goal of the study is to determine whether these behavioral techniques enhance the efficacy of exposure therapy, one of the most empirically supported treatments for anxiety disorders.
Detailed Description
This study tests whether exposure therapy for fear of snakes or spiders is enhanced by the addition of a brief fear retrieval trial prior to treatment, and the use of compound extinction during treatment. The goal of the study is to determine whether these behavioral techniques enhance the efficacy of exposure therapy, one of the most empirically supported treatments for anxiety disorders. Individuals between the ages of 18-65 with elevated fear of spiders or fear of snakes are randomly assigned to one of four treatment conditions (1) standard exposure therapy, (2) exposure therapy with fear retrieval augmentation, (3) exposure therapy with compound extinction augmentation, and (4) exposure therapy with fear retrieval and compound extinction augmentations. All participants undergo an online prescreen and a face-to-face screening assessment to determine eligibility and baseline (pre-treatment) symptom severity. Participants additionally complete assessments directly after treatment (post-treatment), and approximately one week after treatment (follow-up). The pre-treatment assessment occurs 1-14 days prior to treatment, the post-treatment assessment occurs during the treatment visit as soon as the treatment procedure is complete, and the follow-up assessment occurs within a window of 6-14 days after the completion of treatment. Participants complete two behavioral approach tests (in the treatment context and in the generalization context) at pre-treatment, post-treatment, and follow-up. Participants complete a battery of self-report questionnaires at pre-treatment and follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Specific Phobia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exposure with Retrieval
Arm Type
Experimental
Arm Description
Exposure Therapy with Retrieval
Arm Title
Exposure with Compounding
Arm Type
Experimental
Arm Description
Exposure Therapy with Compound Extinction
Arm Title
Exposure with Retrieval and Compounding
Arm Type
Experimental
Arm Description
Exposure Therapy with Retrieval and Compound Extinction
Arm Title
Therapist-Guided Exposure Therapy
Arm Type
Active Comparator
Arm Description
Therapist-guided Exposure Therapy
Intervention Type
Behavioral
Intervention Name(s)
Exposure Therapy with Retrieval
Intervention Description
Participants will receive one-session exposure therapy (up to 92 minutes) for fear of spiders or fear of snakes. Thirty minutes prior to exposure therapy, participants will receive a fear retrieval trial, which is a brief exposure to the feared stimulus (snake or spider). Based on recent basic science research, the fear retrieval trial is expected to enhance the efficacy of exposure therapy.
Intervention Type
Behavioral
Intervention Name(s)
Exposure Therapy with Compound Extinction
Intervention Description
Participants will receive one-session exposure therapy (up to 92 minutes) for fear of spiders or fear of snakes. As a component of therapy, participants will receive compound extinction, which consists of exposure to two feared stimuli simultaneously (two spiders or two snakes). Based on recent basic science research, compound extinction is expected to enhance the efficacy of exposure therapy.
Intervention Type
Behavioral
Intervention Name(s)
Exposure Therapy with Retrieval and Compound Extinction
Intervention Description
Participants will receive one-session exposure therapy (up to 92 minutes) for fear of spiders or fear of snakes. Thirty minutes prior to exposure therapy, participants will receive a brief fear retrieval trial. As a component of therapy, participants will also receive compound extinction.
Intervention Type
Behavioral
Intervention Name(s)
Therapist-guided Exposure Therapy
Intervention Description
Participants will receive one-session exposure therapy (up to 92 minutes) for fear of spiders or fear of snakes.
Primary Outcome Measure Information:
Title
Change in peak subjective fear (0 - 100), behavioral approach (0 - 4), and heart rate reactivity to a live snake/spider not used during treatment (generalization context) from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Secondary Outcome Measure Information:
Title
Change in peak subjective fear (0 - 100), behavioral approach (0 - 4), and heart rate reactivity to a live snake/spider not used during treatment (generalization context) from pre-treatment to post-treatment.
Time Frame
pre-treatment (window of 1-14 days prior to treatment); post-treatment (directly after the treatment procedure is completed)
Title
Change in peak subjective fear (0 - 100), behavioral approach (1 - 8), and heart rate reactivity to a live snake/spider used during treatment (treatment context) from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in peak subjective fear (0 - 100), behavioral approach (1 - 8), and heart rate reactivity to a live snake/spider used during treatment (treatment context) from pre-treatment to post-treatment
Time Frame
pre-treatment (window of 1-14 days prior to treatment); post-treatment (directly after the treatment procedure is completed)
Title
Change in Fear of Snakes/Spiders Questionnaire from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in Snake/Spider Belief Questionnaire from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in Agoraphobic Cognitions Questionnaire for Snake/Spider Phobia from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in Self-Efficacy Questionnaire for Spider/Snake Phobia from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in Armfield and Mattiske Disgust Questionnaire from pre-treatment to follow-up
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)
Title
Change in Lab for the Study of Anxiety Disorders Specific Phobia Diagnostic Questionnaire from pre-treatment to follow-up
Description
change from pre-treatment in current phobic diagnostic status and in level of phobic-related distress and impairment
Time Frame
pre-treatment (window of 1-14 days prior to treatment); follow-up (window of 6-14 days after treatment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 to 65. Speaks English fluently. A score of 70 or higher on the Fear of Snakes/Spiders Questionnaire. Demonstrates avoidance during behavioral approach tests (defined as inability to put palm flat on the bottom of a tank containing a snake/spider, and inability to touch a snake/spider with a bare finger). Exclusion Criteria: Unstable dose of psychotropic medications during the 4 weeks prior to baseline assessment. Currently receiving exposure-based treatment for snake/spider phobia. Currently at risk for suicide.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J Telch, PhD
Organizational Affiliation
University of Texas at Austin
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas at Austin
City
Austin
State/Province
Texas
ZIP/Postal Code
78712
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
33096291
Citation
Lancaster CL, Monfils MH, Telch MJ. Augmenting exposure therapy with pre-extinction fear memory reactivation and deepened extinction: A randomized controlled trial. Behav Res Ther. 2020 Dec;135:103730. doi: 10.1016/j.brat.2020.103730. Epub 2020 Sep 19.
Results Reference
derived

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Enhancing Exposure Therapy for Snake and Spider Phobias

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