Experiential Training for Community Therapists

• ClinicalTrials.gov Identifier: NCT03354975
• Recruitment Status: Completed
• First Posted: November 28, 2017
• Last Update Posted: January 3, 2019
• Sponsor: Temple University
• Collaborator: National Institute of Mental Health (NIMH)
• Information provided by (Responsible Party): Temple University

Study Description

Brief Summary:

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.

Condition or disease	Intervention/treatment	Phase
Anxiety	Behavioral: Experiential Training; Behavioral: Training-As-Usual	Not Applicable

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 28 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Health Services Research
• Official Title: Dissemination of Exposure-Based Treatment for Anxiety: Experiential Training for Community Therapists
• Actual Study Start Date: March 23, 2018
• Actual Primary Completion Date: July 24, 2018
• Actual Study Completion Date: November 1, 2018

Arms and Interventions

Arm	Intervention/treatment
Experimental: Experiential Training	Behavioral: 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	Behavioral: 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.

Outcome Measures

Primary Outcome Measures :

1. 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.
2. 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.

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

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.

Contacts and Locations

Locations

United States, Pennsylvania

Temple University

Philadelphia, Pennsylvania, United States, 19122

Sponsors and Collaborators

Temple University

National Institute of Mental Health (NIMH)

More Information

• Responsible Party: Temple University
• ClinicalTrials.gov Identifier: NCT03354975
• Other Study ID Numbers: 260359; F31MH112211 ( U.S. NIH Grant/Contract )
• First Posted: November 28, 2017
• Last Update Posted: January 3, 2019
• Last Verified: January 2019

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:

Anxiety Disorders; Mental Disorders