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Testing the Efficacy of a Mindfulness- and Acceptance-Based Smartphone App for PTSD: A Randomized Controlled Trial

Primary Purpose

Posttraumatic Stress Disorder

Status
Not yet recruiting
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Mindfulness/Acceptance-Based Smartphone App (MABSA) Intervention
Sponsored by
University of Nevada, Las Vegas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Posttraumatic Stress Disorder focused on measuring Posttraumatic Stress Disorder, mindfulness, acceptance, resilience

Eligibility Criteria

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

Inclusion Criteria:

  • (1) aged 18 years old or older, (2) currently registered as an undergraduate or graduate student, (3) has previous active military service from any U.S. military service branch, (4) has at least daily access to their own Apple iPhone (version 5 or later) or Android phone, and (5) have posttraumatic stress disorder (PTSD) symptoms (must have a score of 33 or above on the PTSD Checklist for DSM-5)

Exclusion Criteria:

  • (1) Those who have a score of 32 or below on the PTSD Checklist for DSM-5 and (2) Those who have a cognitive impairment such as dementia-related disorders.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Mindfulness/Acceptance-Based Smartphone App (MABSA) Intervention Group

    Wait-List Control Group

    Arm Description

    The intervention is 6 weeks in duration. Participants will be asked to listen daily to at least one audio-guided mindfulness meditation embedded in the app. They will also be asked to watch a weekly video lesson on mindfulness and acceptance and will be asked to write a reflection about the video. They will also receive weekly emotional and technical support during the duration of the intervention.

    The control group is a wait-list control group. Participants in the control group will be offered to use the app after 10 weeks of being in the study. The control group participants once they opted to use the app after 10 weeks will only have access to the app for 6 weeks.

    Outcomes

    Primary Outcome Measures

    PTSD
    Changes in posttraumatic stress disorder (PTSD) symptoms based on the PTSD Checklist for DSM-5 (PCL-5)
    Resilience
    Changes in resilience based on the Connor-Davidson Resilience Scale 25
    Mindfulness
    Changes in mindfulness based on the Mindfulness Attention and Awareness Scale
    Experiential Avoidance
    Changes in experiential avoidance based on the Acceptance and Action Questionnaire
    Rumination
    Changes in rumination based on the Rumination Scale

    Secondary Outcome Measures

    PTSD Recovery
    Daily measures of PTSD using the abbreviated PTSD Checklist for DSM-5
    Resilience Progression
    Daily measures of resilience using the abbreviate Connor-Davidson Resilience Scale 10

    Full Information

    First Posted
    April 22, 2021
    Last Updated
    December 9, 2021
    Sponsor
    University of Nevada, Las Vegas
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04861311
    Brief Title
    Testing the Efficacy of a Mindfulness- and Acceptance-Based Smartphone App for PTSD: A Randomized Controlled Trial
    Official Title
    Testing the Efficacy of a Mindfulness- and Acceptance-Based Smartphone App Intervention for College Student Veterans With Posttraumatic Stress Disorder (PTSD): A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 1, 2022 (Anticipated)
    Primary Completion Date
    June 30, 2022 (Anticipated)
    Study Completion Date
    June 30, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Nevada, Las Vegas

    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
    The purpose of the study is to test the feasibility and acceptability of a mindfulness- and acceptance-based smartphone app (MABSA) intervention for college student veterans with posttraumatic stress disorder (PTSD) symptoms. The study will use a randomized controlled trial design of two groups: intervention group of about 30 participants with PTSD and wait-list control group of about 30 participants. The duration of the MABSA intervention is 6 weeks. The following are the outcomes to be measured: resilience, PTSD, mindfulness, experiential avoidance, and rumination.
    Detailed Description
    The objective of the proposed study is to evaluate the feasibility of the Mindfulness/Acceptance-Based Smartphone App (MABSA) intervention in a randomized controlled trial (RCT) environment and to obtain generalized information (i.e., initial efficacy, recruitment, retention, adherence, satisfaction, and usability of the refined intervention). The expected results will provide the foundation for a prospective, fully powered, larger-scale RCT study. We previously developed the MABSA and pilot tested it in a single-arm study. Our central hypothesis is that the refined MABSA intervention would improve intervention satisfaction, app usability, and adherence and positively affect resilience, PTSD, mindfulness, experiential avoidance, and rumination. The specific aims of the proposed study are outlined below. AIM 1: To refine the previously developed MABSA intervention. The 6-week smartphone-delivered program will involve (1) daily audio-guided meditations on various mindfulness and acceptance exercises constructed based on the principles of acceptance and commitment therapy; (2) weekly support and feedback through phone calls and/or texting the intervention facilitators; and (3) ecological momentary assessment (daily monitoring of PTSD and resilience) to monitor the progression of treatment response (i.e., the trajectory of resilience and PTSD recovery). We will obtain qualitative feedback on program content and format through a pilot test of the prototype with a group of eligible college student veterans (N = 4). Upon revising the intervention based on participants' feedback, we will develop the intervention protocol manual for the RCT. AIM 2: To test the feasibility and acceptability of the refined MABSA intervention in a small-scale RCT for a prospective, fully powered, larger-scale RCT study. The small-scale RCT study will involve the following two groups of college student veterans: (1) the MABSA intervention group (N = 30) and the waitlist control group (N = 30). Upon collecting the data on recruitment, retention, adherence, intervention satisfaction, and app usability, we will determine the preliminary efficacy based on the following five outcomes: resilience, PTSD, mindfulness, experiential avoidance, and rumination. Qualitative feedback on the facilitators of and challenges to recruitment, retention, and adherence will be collected via exit interviews.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Posttraumatic Stress Disorder
    Keywords
    Posttraumatic Stress Disorder, mindfulness, acceptance, resilience

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Parallel Assignment
    Model Description
    Mindfulness/Acceptance-Based Smartphone App (MABSA) Intervention Group will use the smartphone app which comprises of audio-guided mindfulness meditations and video lessons. Participants are asked to listen to at least one guided meditation daily and watch one video lesson each week. Participants will also receive a weekly phone call for emotional and technical support. The wait-list control group will have the option to use the app-based intervention after 10 weeks of being in the control group.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    64 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Mindfulness/Acceptance-Based Smartphone App (MABSA) Intervention Group
    Arm Type
    Experimental
    Arm Description
    The intervention is 6 weeks in duration. Participants will be asked to listen daily to at least one audio-guided mindfulness meditation embedded in the app. They will also be asked to watch a weekly video lesson on mindfulness and acceptance and will be asked to write a reflection about the video. They will also receive weekly emotional and technical support during the duration of the intervention.
    Arm Title
    Wait-List Control Group
    Arm Type
    No Intervention
    Arm Description
    The control group is a wait-list control group. Participants in the control group will be offered to use the app after 10 weeks of being in the study. The control group participants once they opted to use the app after 10 weeks will only have access to the app for 6 weeks.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Mindfulness/Acceptance-Based Smartphone App (MABSA) Intervention
    Intervention Description
    The intervention is based on the principles of Acceptance and Commitment Therapy (ACT). Therefore, the intervention is an ACT-based smartphone app delivered for 6 weeks in which participants will be applying the mindfulness and acceptance exercises embedded in the app. The mindfulness and acceptance exercises are audio-guided mindfulness meditations and video lessons about ACT.
    Primary Outcome Measure Information:
    Title
    PTSD
    Description
    Changes in posttraumatic stress disorder (PTSD) symptoms based on the PTSD Checklist for DSM-5 (PCL-5)
    Time Frame
    We will measure PTSD at baseline, mid-intervention (Week 3), post-intervention (Week 6), and at one-month follow-up
    Title
    Resilience
    Description
    Changes in resilience based on the Connor-Davidson Resilience Scale 25
    Time Frame
    We will measure PTSD at baseline, mid-intervention (Week 3), post-intervention (Week 6), and at one-month follow-up
    Title
    Mindfulness
    Description
    Changes in mindfulness based on the Mindfulness Attention and Awareness Scale
    Time Frame
    We will measure PTSD at baseline, mid-intervention (Week 3), post-intervention (Week 6), and at one-month follow-up
    Title
    Experiential Avoidance
    Description
    Changes in experiential avoidance based on the Acceptance and Action Questionnaire
    Time Frame
    We will measure PTSD at baseline, mid-intervention (Week 3), post-intervention (Week 6), and at one-month follow-up
    Title
    Rumination
    Description
    Changes in rumination based on the Rumination Scale
    Time Frame
    We will measure PTSD at baseline, mid-intervention (Week 3), post-intervention (Week 6), and at one-month follow-up
    Secondary Outcome Measure Information:
    Title
    PTSD Recovery
    Description
    Daily measures of PTSD using the abbreviated PTSD Checklist for DSM-5
    Time Frame
    We will measure PTSD daily using the app (ecological momentary assessment)
    Title
    Resilience Progression
    Description
    Daily measures of resilience using the abbreviate Connor-Davidson Resilience Scale 10
    Time Frame
    We will measure resilience daily using the app (ecological momentary assessment)
    Other Pre-specified Outcome Measures:
    Title
    Intervention Satisfaction
    Description
    Satisfaction with the intervention particularly on the areas of: overall satisfaction, perceived helpfulness, comprehension, intentions to use, and perceived fit
    Time Frame
    We will measure intervention satisfaction at mid-intervention (Week 3) and post-intervention (Week 6)
    Title
    System Usability
    Description
    Perceived usability of the app using the System Usability Scale
    Time Frame
    We will measure perceived usability of the app at mid-intervention (Week 3) and post-intervention (Week 6)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: (1) aged 18 years old or older, (2) currently registered as an undergraduate or graduate student, (3) has previous active military service from any U.S. military service branch, (4) has at least daily access to their own Apple iPhone (version 5 or later) or Android phone, and (5) have posttraumatic stress disorder (PTSD) symptoms (must have a score of 33 or above on the PTSD Checklist for DSM-5) Exclusion Criteria: (1) Those who have a score of 32 or below on the PTSD Checklist for DSM-5 and (2) Those who have a cognitive impairment such as dementia-related disorders.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Andrew T Reyes, PhD
    Phone
    702-895-5094
    Email
    andrewthomas.reyes@unlv.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Andrew T Reyes, PhD
    Organizational Affiliation
    University of Nevada, Las Vegas
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    32248935
    Citation
    Reyes AT, Bhatta TR, Muthukumar V, Gangozo WJ. Testing the acceptability and initial efficacy of a smartphone-app mindfulness intervention for college student veterans with PTSD. Arch Psychiatr Nurs. 2020 Apr;34(2):58-66. doi: 10.1016/j.apnu.2020.02.004. Epub 2020 Feb 18.
    Results Reference
    background
    PubMed Identifier
    33280672
    Citation
    Reyes AT, Serafica R, Sojobi A. College student veterans' experience with a mindfulness- and acceptance-based mobile app intervention for PTSD: A qualitative study. Arch Psychiatr Nurs. 2020 Dec;34(6):497-506. doi: 10.1016/j.apnu.2020.09.005. Epub 2020 Sep 11.
    Results Reference
    background

    Learn more about this trial

    Testing the Efficacy of a Mindfulness- and Acceptance-Based Smartphone App for PTSD: A Randomized Controlled Trial

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