- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03354975
Experiential Training for Community Therapists
January 2, 2019 updated by: Temple University
Dissemination of Exposure-Based Treatment for Anxiety: Experiential Training for Community Therapists
The primary goal of this study is to evaluate the feasibility and acceptability of employing an experiential training approach that targets community mental health therapists' attitudes toward and use of exposure therapy.
In addition to assessing attitudes and use of exposure therapy, the study will evaluate the feasibility of recruitment, randomization, retention, and assessment processes, as well as the acceptability of the experiential training relative to training-as-usual.
To assess these outcomes, community therapists will be randomized to experiential training or training-as-usual.
A subset of therapists from each arm will also complete qualitative interviews to further assess acceptability of the training approaches.
The training-as-usual condition will include a traditional one-day workshop that focuses on principles of exposure and incorporates active learning strategies.
The experiential training will include a one-day workshop that teaches principles of exposure and has therapists themselves undergo a one-session phobia treatment for spiders.
Therapists in both training conditions will be asked to attend weekly consultation phone calls for a three-month period following the trainings.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
28
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
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Philadelphia, Pennsylvania, United States, 19122
- Temple University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participants will be aged 21 and older with degrees (masters or doctorate) in a mental health field. They must be working in a community mental health clinic, currently treating at least one client with anxiety, and planning to continue providing therapy to at least one client with anxiety for the duration of the study. Participants must be interested in participating in a training workshop and able to commit to the time requirements for study completion. They must also be willing to provide an email or mailing address to complete study-related surveys. Finally, they must be able to read and speak English.
Exclusion Criteria:
- Participants cannot have previously attended a full day (8+ hours) workshop on exposure-based treatments for anxiety.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experiential Training
|
Participants in the experiential training will be provided with information about using exposure therapy to treat patients with anxiety via lecture-style teaching.
Then, they will themselves undergo a one-session phobia treatment for spiders.
|
Active Comparator: Training-as-usual
|
The training-as-usual condition will incorporate passive and active learning components.
The first half of the training will include lecture-style teaching about using exposure therapy to treat patients with anxiety.
The second half of training will incorporate active learning components (e.g., role plays) to reinforce concepts discussed in the first half of training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline Therapist Beliefs about Exposure Scale (TBES) at 3-month follow-up
Time Frame: Pre-training; 3-month follow-up
|
The Therapist Beliefs about Exposure Scale is a 21-item self-report measure that assesses therapists' negative beliefs about exposure therapy.
Agreement with each item is rated on a 5-point scale ranging from 0 (disagree strongly) to 4 (agree strongly), yielding a total score ranging from 0 to 84.
Higher scores indicate more negative beliefs about exposure.
|
Pre-training; 3-month follow-up
|
Change from baseline Exposure Therapy Clinical Use Survey (ETCUS) at 3-month follow-up
Time Frame: Pre-training; 3-month follow-up
|
The ETCUS measures therapist-reported use of nine exposure therapy procedures, such as providing the rationale for exposure therapy, creating a hierarchy, and completing in-vivo exposures.
|
Pre-training; 3-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 23, 2018
Primary Completion (Actual)
July 24, 2018
Study Completion (Actual)
November 1, 2018
Study Registration Dates
First Submitted
November 13, 2017
First Submitted That Met QC Criteria
November 27, 2017
First Posted (Actual)
November 28, 2017
Study Record Updates
Last Update Posted (Actual)
January 3, 2019
Last Update Submitted That Met QC Criteria
January 2, 2019
Last Verified
January 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 260359
- F31MH112211 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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