BEAST: Behavioral Economics Intervention to Increase Treatment Seeking in the National Guard

Sponsor
University of Southern Mississippi (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04098588
Collaborator
Military Suicide Research Consortium (Other)
112
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2
27.5
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Study Details

Study Description

Brief Summary

The study is a randomized controlled trial of a single-session behavioral economics (research combining the areas of economics, social psychology, and cognitive psychology) intervention (i.e., BEAST) is a"warrior-culture" consistent (i.e., focusing on positive soldier traits, solving practical problems), highly scalable, and extremely brief (10-minute) intervention to encourage treatment seeking among MS National Guard problems for various life stressors. Participants will be 112 National Guard members. It is hypothesized that BEAST will lead to more self-reported motivation to seek treatment and more actual treatment seeking behavior.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: BEAST
  • Behavioral: Descriptive Feedback
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Behavioral Economics Intervention to Increase Treatment Seeking in the National Guard
Actual Study Start Date :
Dec 15, 2019
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Mar 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: BEAST

There are 3 parts to BEAST. Part 1 involves the Behavioral Nudge technique using previously collected injunctive and descriptive norms from a National Guard sample. Soldiers will be given a customized feedback form that shows norms relevant to the target behavior they selected. The soldier will be given a chance to ask any follow-up questions. Part 2 of the intervention focuses on the principle of targeting others, considering how a change would impact those closest to them. Part 3 will utilize the Reciprocal Concessions procedure combined with the Reducing Barriers technique.

Behavioral: BEAST
See Arm Description

Active Comparator: Descriptive Feedback

This condition will involve a presentation of descriptive data based on the soldiers' tests scores and an opportunity to ask any follow-up questions. This process is a component of some behavioral change interventions (e.g., motivational interviewing); therefore this should be a more useful control condition (mirroring parts 1 and 2 of the active condition) versus a more passive or waitlist control condition. Participants in the control condition will also be given standard referral information to the USM Psychology Clinic (mirroring part 3 of the active condition).

Behavioral: Descriptive Feedback
See Arm Description

Outcome Measures

Primary Outcome Measures

  1. Psychosocial Treatments Interview-Revised [1 month post intervention]

    Measure changes in treatment seeking behavior

  2. University of Rhode Island Change Assessment [1 month post intervention]

    Measure motivation to change the target behavior

Secondary Outcome Measures

  1. Psychosocial Treatments Interview-Revised [3 month post intervention]

    Measure changes in treatment seeking behavior

  2. University of Rhode Island Change Assessment [3 month post intervention]

    Measure motivation to change the target behavior

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • National Guard active

  • 17 ACSS-FAD

Exclusion Criteria:
  • those determined by military or study personnel to be actively psychotic, manic, or who are imminently suicidal and in need of emergency services.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Southern Mississippi Hattiesburg Mississippi United States 39406-0002

Sponsors and Collaborators

  • University of Southern Mississippi
  • Military Suicide Research Consortium

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Southern Mississippi
ClinicalTrials.gov Identifier:
NCT04098588
Other Study ID Numbers:
  • W81XWH-16-2-0003
First Posted:
Sep 23, 2019
Last Update Posted:
May 10, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 10, 2021