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CAREN vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial (CARE4PTSD)

Primary Purpose

Stress Disorders, Post-Traumatic

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR)
Sponsored by
Uniformed Services University of the Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stress Disorders, Post-Traumatic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Service member, veteran, retiree, or DEERS-eligible dependent, male or female, at least 18 years or older
  • Diagnosis of PTSD, as confirmed by the CAPS-5
  • Able to ambulate with contact guard assistance or less, and walk unassisted on a treadmill, at a normal pace, for up to 90 minutes continuously

Exclusion Criteria:

  • History of epilepsy or a seizure disorder, other than febrile seizures that occurred during childhood and have not recurred since
  • History of a psychotic disorder, bipolar disorder, or active suicidal or homicidal ideation
  • Use of benzodiazepines on a regular basis within the previous 30 days

Sites / Locations

  • Uniformed Services UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

3MDR delivered via Augmented Reality Head Mounted Display

3MDR delivered in the Computer Assisted Rehabilitation Environment (CAREN)

Arm Description

All participants will complete 10-14 treatment sessions (three preparatory sessions, 6 to 10 3MDR therapy sessions, and one concluding session), led by a therapist who has completed training and/or is experienced in the conduct of this form of therapy.

All participants will complete 10-14 treatment sessions (three preparatory sessions, 6 to 10 3MDR therapy sessions, and one concluding session), led by a therapist who has completed training and/or is experienced in the conduct of this form of therapy.

Outcomes

Primary Outcome Measures

Clinician Administered PTSD scale for DSM5 (CAPS-5)
The primary outcome measure will be the Clinician Administered PTSD scale for DSM5 (CAPS-5), the gold standard measure for PTSD diagnosis, to assess PTSD symptom severity.
PTSD Checklist for DSM5 (PCL5)
The PTSD Checklist for DSM5 (PCL5), a well-validated 20-item self-report measure of PTSD symptom severity.

Secondary Outcome Measures

Patient Health Questionnaire Depression module (PHQ-9)
The Patient Health Questionnaire Depression module (PHQ-9) is a well-validated instrument for assessing depression symptom severity.
Insomnia Severity Index (ISI)
The Insomnia Severity Index (ISI) is a validated method with which to evaluate insomnia and sleep difficulties.
Neurobehavioral Symptom Inventory (NSI)
The Neurobehavioral Symptom Inventory (NSI) is a validated instrument for assessing postconcussive symptom severity.
Brief Resilience Scale (BRS)
The Brief Resilience Scale (BRS) is a validated instrument used to assess resilience.

Full Information

First Posted
August 11, 2021
Last Updated
February 14, 2022
Sponsor
Uniformed Services University of the Health Sciences
Collaborators
Center for Neuroscience and Regenerative Medicine, USUHS, Center for Rehabilitation Sciences Research, USUHS
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1. Study Identification

Unique Protocol Identification Number
NCT05244564
Brief Title
CAREN vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial
Acronym
CARE4PTSD
Official Title
CAREN Versus Augmented Reality: Expanding 3MDR Therapy for PTSD
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 20, 2021 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Uniformed Services University of the Health Sciences
Collaborators
Center for Neuroscience and Regenerative Medicine, USUHS, Center for Rehabilitation Sciences Research, USUHS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a prospective randomized controlled trial comparing two ways of delivering Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) therapy for posttraumatic stress disorder (PTSD). The study seeks 60 volunteers who have PTSD and are eligible for care in the Department of Defense healthcare system. There will be 10-14 therapy sessions that are 60-90 minutes long, about once a week, and symptoms will be assessed before and after the therapy as well as 3 and 6 months after completing therapy. 3MDR asks you to choose pictures and music that are integrated into a virtual reality environment. You will be walking on a treadmill throughout each therapy session, while the therapist stands next to the treadmill and asks you questions about the pictures you chose.
Detailed Description
Posttraumatic stress disorder (PTSD) frequently occurs after combat and other life-threatening or traumatic events. Currently available treatments for PTSD often have a brief, limited effect, or are not well-tolerated. Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) is a new and unique treatment for PTSD that has been commonly referred to as "walk and talk" therapy, because you walk on a treadmill as you work through your symptoms with a therapist. 3MDR also combines some features of virtual reality exposure therapy (VRET) and Eye Movement Desensitization and Reprocessing (EMDR), and has usually been conducted in the Computer Assisted Rehabilitation Environment (CAREN), a sophisticated virtual reality "cave". Previous clinical studies by us and others across several nations have proven the effectiveness of the 3MDR approach in treating symptoms of PTSD. However, the CAREN is large, expensive (~$1 million), and only available in a few places around the world. To try to make 3MDR available to more people, this study will compare how much PTSD symptoms change with 3MDR conducted by 1) walking on a regular treadmill while wearing goggles (known as augmented reality head-mounted display, or AR HMD) that allow you to see the treadmill and things around you in the real world, while also seeing pictures in a virtual world, with 2) walking inside the cave-like fully immersive virtual reality environment of the CAREN. There will be a total of 60 participants in the study, all at Uniformed Services University/Walter Reed National Military Medical Center. After completing the informed consent process, all participants will be evaluated to confirm that they meet criteria for PTSD. There will be two introductory sessions where you meet the therapist you will be working with, and they will help you choose music and pictures that will be used in your later sessions. These introductory sessions can be done in person or virtually. In the third session you will try walking on the treadmill with a sample picture, either in the CAREN or with the AR HMD, depending on which approach you are randomized to receive-you have an equal chance of either. Starting with the 4th session, you will be talking through the pictures you have chosen, with your therapist. You will spend about 10 minutes on each picture, and do 5 or 6 pictures each session, and will do this through session 9. After that, you will complete a brief questionnaire about your symptoms. If you still have significant symptoms, you will do another 2 sessions of talking through your pictures, then do another questionnaire, and again will do two more sessions if you still have symptoms. There is then one final wrap-up session, which can be done either in person or virtually, to discuss how you did with the therapy, and whether you might need any more therapy to help you if you have any symptoms left to address. Depending on how quickly your symptoms improve, you may do a total of 10, 12 or 14 therapy sessions in this study. After you have finished the therapy sessions, you will again be assessed to see how much your symptoms have improved, and you will do this again 3 and 6 months later.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress Disorders, Post-Traumatic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
All receive the 3MDR intervention, but are randomized to delivery in the CAREN vs via AR HMD
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
3MDR delivered via Augmented Reality Head Mounted Display
Arm Type
Experimental
Arm Description
All participants will complete 10-14 treatment sessions (three preparatory sessions, 6 to 10 3MDR therapy sessions, and one concluding session), led by a therapist who has completed training and/or is experienced in the conduct of this form of therapy.
Arm Title
3MDR delivered in the Computer Assisted Rehabilitation Environment (CAREN)
Arm Type
Active Comparator
Arm Description
All participants will complete 10-14 treatment sessions (three preparatory sessions, 6 to 10 3MDR therapy sessions, and one concluding session), led by a therapist who has completed training and/or is experienced in the conduct of this form of therapy.
Intervention Type
Other
Intervention Name(s)
Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR)
Intervention Description
"Walk and talk" therapy, walking on a treadmill while talking with a therapist about self-chosen pictures representative of one's trauma; 3MDR also includes some features of virtual reality exposure therapy (VRET) and Eye Movement Desensitization and Reprocessing (EMDR) therapy.
Primary Outcome Measure Information:
Title
Clinician Administered PTSD scale for DSM5 (CAPS-5)
Description
The primary outcome measure will be the Clinician Administered PTSD scale for DSM5 (CAPS-5), the gold standard measure for PTSD diagnosis, to assess PTSD symptom severity.
Time Frame
3 months
Title
PTSD Checklist for DSM5 (PCL5)
Description
The PTSD Checklist for DSM5 (PCL5), a well-validated 20-item self-report measure of PTSD symptom severity.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Patient Health Questionnaire Depression module (PHQ-9)
Description
The Patient Health Questionnaire Depression module (PHQ-9) is a well-validated instrument for assessing depression symptom severity.
Time Frame
3 months
Title
Insomnia Severity Index (ISI)
Description
The Insomnia Severity Index (ISI) is a validated method with which to evaluate insomnia and sleep difficulties.
Time Frame
3 months
Title
Neurobehavioral Symptom Inventory (NSI)
Description
The Neurobehavioral Symptom Inventory (NSI) is a validated instrument for assessing postconcussive symptom severity.
Time Frame
3 months
Title
Brief Resilience Scale (BRS)
Description
The Brief Resilience Scale (BRS) is a validated instrument used to assess resilience.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Service member, veteran, retiree, or DEERS-eligible dependent, male or female, at least 18 years or older Diagnosis of PTSD, as confirmed by the CAPS-5 Able to ambulate with contact guard assistance or less, and walk unassisted on a treadmill, at a normal pace, for up to 90 minutes continuously Exclusion Criteria: History of epilepsy or a seizure disorder, other than febrile seizures that occurred during childhood and have not recurred since History of a psychotic disorder, bipolar disorder, or active suicidal or homicidal ideation Use of benzodiazepines on a regular basis within the previous 30 days
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hannah Attalah, BA
Phone
301-412-8187
Email
care4ptsd@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Roy, MD, MPH
Phone
301-295-9601
Email
michael.roy@usuhs.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Roy, MD, MPH
Organizational Affiliation
Unformed Services University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Uniformed Services University
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20814
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hannah Atallah, BA
Phone
301-412-8187
Email
hannah.atallah.ctr@usuhs.edu

12. IPD Sharing Statement

Learn more about this trial

CAREN vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial

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