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Adaptation of the STAIR-NT for First Responders

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Florida State University

Status

Begins enrollment in 3 months

Conditions

PTSD - Post Traumatic Stress Disorder
TBI-Traumatic Brain Injury

Treatments

Behavioral: Adapted STAIR-NT

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT07212140
STUDY00005143 (Other Identifier)
HT9425-24-1-0782 (Other Grant/Funding Number)

Details and patient eligibility

About

This study is a randomized controlled pilot examining the implementation of an adapted intervention, Skills Training in Affective and Interpersonal Regulation-Narrative Therapy (STAIR-NT), among a first responder population with a history of TBI and PTSD.

Full description

The primary objective of the study is to implement and evaluate the effectiveness of an evidence-based intervention, STAIR-NT, which will be adapted with Goal Management Training (GMT). A small-scale randomized control pilot will be conducted using the adapted intervention to examine implementation (i.e., feasibility, acceptability) and improvements in short-term PTSD, as well as secondary mental health outcomes (e.g., anxiety, and depression symptoms, substance misuse) among a first responder population with a history of TBI and PTSD.

Enrollment

80 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older
  • be a first responder within the state of Minnesota
  • have a history of a TBI
  • screen for PTSD.

Exclusion criteria

  • Does not meet inclusion criteria.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Adapted STAIR-NT Intervention
Experimental group
Description:
Participants in this arm will receive the adapted version of Skills Training in Affective and Interpersonal Regulation-Narrative Therapy (STAIR-NT).
Treatment:
Behavioral: Adapted STAIR-NT
Treatment as usual (TAU)
No Intervention group
Description:
Participants in this arm will receive treatment as usual.

Trial contacts and locations

1

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Central trial contact

Joseph Schwartz, PhD; Tanya Renn, PhD

Data sourced from clinicaltrials.gov

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