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Stress Disorders, Post-TraumaticHBTMHNCT02295410

The Effects of Home-Based Telemental Health for Rural Veterans With PTSD

An observational study of Stress Disorders, Post-Traumatic, run by VA Pacific Islands Health Care System at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The intent of this study is to assess whether cognitive functioning improves as Post-Traumatic Stress Disorder (PTSD) symptoms decrease as a step toward developing an objective measure of PTSD improvement. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Stress Disorders, Post-Traumatic
What is being tested?
CPT
How many people
66 participants
Where
1 siteUnited States
Study dates
May 2013to Mar 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Up to 200 Veterans with PTSD who have been referred by their CBOC to the HBTMH PTSD clinic or a VA Clinic will be enrolled in this research study. This sample size is based on the number of treatment subjects intended to be treated by the HBTMH clinic, the VA clinic, and the estimated numbers of subjects who will be ineligible or choose not to participate in the HBTMH treatment. This number should be sufficient given past effect size differences between HBTMH treatment and TAU (Cohen's d effect size averaging about 1.0). It will also allow us to measure changes in psychological and cognitive functioning within treatment subjects over time.

Who may be able to join

  • Participants must have a referral to the HBTMH Clinic or VA clinic for PTSD treatment as well as:
  • ability to use a keyboard
  • the ability to demonstrate a thorough understanding of the study and willingness to participate
  • comfort using a tablet device and the Internet, or willingness to learn
  • have agreed to return the tablet and headset after the study (TAU and HBTMH-only)
  • adequate (or corrected) vision and hearing
  • ability to read and write at an 8th grade level or higher.

Who cannot join

  • clinical disqualification (current psychosis, active homicidal or suicidal intent or within the past six months)
  • significant cognitive impairment as determined by inability to sufficiently comprehend the study goals, risks and benefits.
  • To determine this, potential research participants will be asked to summarize the study as explained to them and as presented by the Study Fact Sheet/Consent Form as applicable.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • VA Pacific Island Health Care System

    Honolulu, Hawaii, 96819

Other trials in United States

About this study

The intent of this study is to assess whether cognitive functioning improves as Post-Traumatic Stress Disorder (PTSD) symptoms decrease as a step toward developing an objective measure of PTSD improvement. The study also evaluates the feasibility and effectiveness of home-based telemental health care (HBTMH) compared to usual care in the treatment of rural Veterans with posttraumatic stress disorder (PTSD). For this assessment-only study, the investigators plan to assess approximately 200 Veterans in total, of which 150 will be undergoing regular evidenced-based therapy (EBT) for PTSD, and 50 will be receiving other treatment as usual (TAU). The 150 veterans in the EBT group will be undergoing Cognitive Processing Therapy (CPT), Cognitive-Behavioral Couple Therapy (CBCT), Prolonged Exposure (PE), or Seeking Safety (SS) treatment for PTSD in clinic or via home-based telemental health (HBTMH). The study will also assess a comparison group of approximately 50 rural Veterans with PTSD diagnoses who are receiving treatment as usual (TAU) (neither EBT nor HBTMH). The HBTMH patients will be recruited from an Office of Rural Health (ORH) funded project to VA Pacific Island Health Care System (VAPIHCS), based at the National Center for PTSD (NCPTSD) and funded to offer 100 rural Veterans mental health treatment in their homes. This research protocol intends to assess rural veterans with PTSD who are being seen within this clinic versus those who have been referred for HBTMH yet who are ineligible for pragmatic purposes, with outcomes including feasibility, cost-effectiveness, and clinical effectiveness. The cognitive change will also be measured in patients with PTSD diagnoses receiving EBT PTSD treatment at VA clinics in the Pacific Islands.

Read the detailed description

The Office of Rural Health has funded the VA Pacific Islands Healthcare System (VAPIHCS) to provide HBTMH for rural veterans diagnosed by a mental health provider as having PTSD. VAPIHCS serves an area about the size of the continental United States. Outside of Honolulu, there are few mental health specialists to serve Veterans with PTSD and common comorbid disorders, such as traumatic brain injury (TBI), pain, insomnia, and substance abuse. Moreover, many such Veterans have difficulty following-up for services at Community-Based Outpatient Clinics (CBOCs) due to psychological or physical limitations, transportation, work schedule, or stigma.

Cost is another reason to develop a HBTMH approach. Seventy percent of those who complete a course of Evidence Based Therapy (EBT) significantly improve their symptoms, with most no longer carrying the diagnosis following such treatments (Bradley, Greene, Russ, Dutra, \& Westen, 2005). However those who lack access to EBTs, especially those with polytraumas, have a low chance of recovery (Elhers \& Clark, 2008; Lyons \& Keane, 1992). The lack of specialists in these regions means that the Veterans continue to suffer with PTSD and related disorders far longer than if specialized care were available. Sending experts to these areas is costly, and inefficient. The cost and difficulty for highly rural Veterans to travel for weekly appointments to a CBOC that lacks expertise in EBT for PTSD and treating Veterans with polytrauma has minimal value. Finally, the no-show rate for such Veterans can run well above 15%, whereas research with HBTMH has no-show rates of less than 4% (http://conference.avapl.org/pubs/2012%20Conference%20Presentations/HBTMH%20SOP_Shore_11-12-11%20copy.pdf)

To improve services for Veterans, the VA provides telehealth options at its CBOC locations in the Pacific Islands. Many patients live too far from the CBOC or prefer to receive mental health treatment in the comfort of their own homes. HBTMH technology, such as televideo sessions between a home-based patient and their mental healthcare provider, has been successfully implemented in the VA (e.g. throughout VISN 20 and VISN 7) and in the Department of Defense (DOD). VAPIHCS was funded by the ORH to provide evidence-based specialty treatment via HBTMH to rural Veterans with PTSD who would not otherwise have such treatment available to them. The clinical project is funded to provide up to 100 rural patients who were referred by their CBOC providers to this specialty clinic for HBTMH PTSD treatment. This VAPIHCS clinic provides evidence-based treatment to eligible veterans in their homes via televideo by clinicians currently based at the NCPTSD. Only ORH-funded VAPIHCS clinical staff will provide treatment to the PTSD patients who choose to and are eligible to receive the home-based telemental health. Veterans are eligible for this VAPIHCS-HBTMH clinic if they have been diagnosed with PTSD by a licensed mental health provider at a CBOC, or are referred by a CBOC (via clinical consult).

In order to initially evaluate the effectiveness of HBTMH, the current research study will evaluate veterans participating in the VAPIHCS-HBTMH clinic compared to Treatment as Usual (TAU - those who were referred to the clinic, however either refused to participate in this type of clinical care or were ineligible to be part of this clinic due to structural difficulties (no 4G in their area, can't type, lack of nearby emergency services, etc). Thus, this protocol is assessment only, and is separate from the treatment provided to the rural Veterans.

Currently, there are no standardized, objective assessments available for determining impairment and improvement of PTSD. The Defense Automated Neurobehavioral Assessment (DANA) is a clinical decision support tool developed for the Department of Defense (DoD) for field and clinic-based neurobehavioral functioning. This neurobehavioral assessment system was developed on the assumption that various risk factors (PTSD, Depression, Insomnia, anger, pain, etc.) lead to significantly slower and less accurate (throughput) performance on cognitive tests. The primary goal of DANA is to assist providers in determining level of functioning and to track recovery over time. An important purpose of this study is to collect longitudinal data from patients receiving EBT (both in clinics and through HBTMH) in order to assess whether cognitive functioning improves as PTSD symptoms decrease with treatment. This information will provide support for DANA's validity as an objective measure of PTSD impairment. The study also plans to determine the sensitivity and specificity of DANA neurocognitive measures in determining changes in cognitive functioning within PTSD patients engaged in EBT over time.

The proposed project aims to examine the effectiveness of an empirically based trauma-focused treatment intervention delivered via video conferencing to the home. This project aims to:

Objective 1: Examine the feasibility of HBTMH compared to treatment as usual.

Objective 2: Compare the effectiveness of HBTMH compared to treatment as usual.

Objective 3: Determine predictors of successful treatment outcomes (including treatment completion and clinically significant reduction in PTSD and related symptoms).

Objective 4: Determine the sensitivity and specificity of Defense Automated Neurobehavioral Assessment (DANA) neurocognitive measures in determining changes in psychological functioning within subjects over time.

Being tested
CPT
Keywords
Assessment, PTSD, Veterans
Medical subject headings
Stress Disorders, Post-Traumatic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CPTBehavioural

    Also called Cognitive Processing Therapy

Study groups in NCT02295410
Study groupRoleWhat they receive
Engaged in Home-Based CPTHome-Based Telemental Health-Patients undergoing Home-Based CPT for PTSD
Receives: Behavioral: CPT
ComparisonTreatment as Usual (TAU) Patients NOT receiving regular CPT or other evidence-based therapy for PTSD.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in PCL-M

    Posttraumatic Stress Disorder Checklist- Military (PCL-M) [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

Secondary outcomes (7)
  1. Change in Simple Reaction Time Throughput

    Computerized Neurocognitive Test of Reaction time speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  2. Change in Procedural Reaction Time Throughput

    Computerized Neurocognitive Test of Procedural Reaction time speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  3. Go-No Go Throughput

    Computerized Neurocognitive Test of IsFoe or IsNotFoe for speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  4. Change in Code Substitution (Learning and Recall) Throughput

    Computerized Neurocognitive Test of Code Substitution (Learning and Recall) for speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  5. Change in Spacial Processing Throughput

    Computerized Neurocognitive Test of Spacial Processing for speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  6. Change in Matching to Sample Throughput

    Computerized Neurocognitive Test of Matching to Sample for speed and accuracy. [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

  7. Change in PHQ-9

    Patient Health Questionnaire -9 for measuring depression [repeated measure]

    Measured: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Nov 2014 (estimated)
  2. Study startMay 2013
  3. Primary completionMar 2015
  4. Study completionMar 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
66 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02295410
Sponsor's protocol ID
2013-03/JLS 0007
Acronym
HBTMH
Status last verified
Mar 2016
First submitted
12 Nov 2014
Last updated
6 Nov 2017
Results posted
No
Data monitoring committee
No

Publications

  • Lathan C, Spira JL, Bleiberg J, Vice J, Tsao JW. Defense Automated Neurobehavioral Assessment (DANA)-psychometric properties of a new field-deployable neurocognitive assessment tool. Mil Med. 2013 Apr;178(4):365-71. doi: 10.7205/MILMED-D-12-00438.

    PubMed 23707818
  • Spira JL, Lathan CE, Bleiberg J, Tsao JW. The impact of multiple concussions on emotional distress, post-concussive symptoms, and neurocognitive functioning in active duty United States marines independent of combat exposure or emotional distress. J Neurotrauma. 2014 Nov 15;31(22):1823-34. doi: 10.1089/neu.2014.3363. Epub 2014 Oct 9.

    PubMed 25003552

Questions about this trial

What is this clinical trial studying?

An observational study of Stress Disorders, Post-Traumatic, run by VA Pacific Islands Health Care System at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Nov 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in PCL-M (time frame: approximately 0, 4 and 8 weeks depending on the number of CPT sessions completed.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02295410, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2017.

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