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N/A N=29

Using Mobile Technology to Address the Trauma Mental Health Treatment Gap

Post Traumatic Stress Disorder

Enrolled (actual)
29
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: Aim 1: Evaluation of Educational Materials — 3; 2; 4; 2 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Aim 2: BounceBack Now (BBN) for Trauma Informed Care Deployment (Behavioral); Aim 1 Participant Focus Groups (Behavioral); Aim 1 BHP Focus Groups (Behavioral); Aim 2: BHP, Provider, Staff and Admin Focus Groups (Behavioral); Aim 2 : Participant Focus Group (Behavioral)
Age
Adult, Older Adult · 19+ yrs
Sex
All
Sponsor
University of Nebraska
Primary completion
Mar 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Aim 1: Evaluation of Educational Materials
3; 2; 4; 2; 3; 2
PRIMARY
Aim 2: Feasibility
4; 10; 2; 7; 2; 8
PRIMARY
Aim 2: Acceptability: App Use
6
PRIMARY
Aim 2:Usability
113.8
PRIMARY
Aim 2: Patient Burden
4.17

Summary

BounceBack Now (BBN) is a self-help, trauma-focused mental health mobile application (app) with automated assessment with treatment guidance and in-app evidence-based treatment support for depression, post-traumatic stress disorder (PTSD), sleep difficulties, and anxiety. BBN contains many of the necessary components to promote self-management of these conditions. Investigators will evaluate the app's feasibility and acceptability among under served participants (e.g., African Americans and participants with lower socioeconomic status) with trauma histories in an integrated primary care (IPC) setting. There are two specific aims: 1) to develop educational materials for patients and behavioral health providers for BBN in IPC, and 2) to conduct a pilot trial of BBN for participants with trauma histories in an IPC setting. For Aim 1, focus groups with behavioral health providers and participants will be conducted to obtain feedback about BBN and training materials. For Aim 2, a feasibility study with 15 participants will be conducted to identify and address any procedural issues and to refine the protocol before conducting the full-scale study.

Eligibility Criteria

Inclusion Criteria

Behavioral Health Providers:

  • 19 years and older

Participants:

  • 19 years and older
  • Newly referred to a behavioral health provider at the Fontanelle or Midtown Clinic
  • Own a smart phone

Exclusion Criteria

Behavioral Health Providers:

  • 18 years and younger

Participants:

  • 18 years and younger
  • Referred to a behavioral health provider in the past year
  • Does not own a smart phone
  • Score 2 points or lower on the Adverse Childhood Experience screening
  • High suicidality based on a clinical assessment by the behavioral health provider
  • Having neurocognitive conditions either assessed by a primary care provider or diagnostic code for neurocognitive condition found in the patient note or Electronic Health Record (EHR)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05374408). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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