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Does Adding a Tailored Cognitive Behavioral Therapy (CBT) Mobile Skills App Mediate Rates of Depression (CBT Mobile-V)

Primary Purpose

Depression

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CBT MobileWork-V plus CBT
CBT alone
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Depression, OEF/OIF, Mobile Apps, Cognitive Behavioral Therapy

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Veteran of OEF/OIF/OND deployments
  • Depressive severity of at least 10 on the PHQ-9 at screening (Patient may also have a DSM-5 56 diagnosis of unipolar Major Depression; PTSD; any anxiety disorder; substance/alcohol abuse; or adjustment disorder)
  • Ability to read at the eighth grade level and to provide informed consent
  • Patients may be taking antidepressants or antianxiety medications where dose has been stable for at least 4 weeks prior to screening evaluation
  • Must have an Android smartphone
  • Must be willing to be audio-taped for fidelity ratings

Exclusion Criteria:

  • Diagnoses of schizophrenia, schizo-affective, bipolar, or other psychotic disorder
  • Serious suicidal risk (Patient responds positively to PHQ-9 question #9) See B.3.4.1.
  • Severe PTSD (Score greater than 51 on PTSD Checklist for DSM-5)
  • Severe substance or alcohol dependence (meets DSM-5 criteria of severe)

Sites / Locations

  • Washington DC VA Medical Center, Washington, DC
  • Jesse Brown VA Medical Center, Chicago, IL
  • Rehabilitation R&D Service, Baltimore, MD
  • Minneapolis VA Health Care System, Minneapolis, MN
  • Coatesville VA Medical Center, Coatesville, PARecruiting
  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PARecruiting
  • VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PARecruiting
  • VA North Texas Health Care System Dallas VA Medical Center, Dallas, TXRecruiting
  • Clement J. Zablocki VA Medical Center, Milwaukee, WIRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CBT-D augmented with CBT MobileWork-V

CBT-D

Arm Description

Patients randomized to this condition will receive CBT-D as usual plus access to CBT MobileWork-V, a comprehensive tailored smartphone app for CBT skills practice for OEF/OIF Veterans.

Patients randomized to CBT-D will receive CBT-D as usual only.

Outcomes

Primary Outcome Measures

Skills of Cognitive Therapy (Patient Version) Change
8-item self-report (patient version) and therapist-rated instrument of a 5-point Likert-type scale ranging from (never) to 5 (always or when needed) assesses patients understanding and use of basic CBT skills.

Secondary Outcome Measures

Patient Health Questionnaire (PHQ-9) Change
9-item questionnaire scoring the DSM-IV criteria for depression as not at all (0) to nearly every day (3); scores of 1 to 4 indicate minimal symptoms while 20 indicates severe depression

Full Information

First Posted
June 20, 2019
Last Updated
September 13, 2023
Sponsor
VA Office of Research and Development
Collaborators
Corporal Michael J. Crescenz VA Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04002063
Brief Title
Does Adding a Tailored Cognitive Behavioral Therapy (CBT) Mobile Skills App Mediate Rates of Depression
Acronym
CBT Mobile-V
Official Title
Does Adding a Tailored Cognitive Behavioral Therapy (CBT) Mobile Skills App Mediate Higher Rates of Depression Recovery, Adjustment, and Quality of Life inOEF/OIF Veterans Compared to Standard CBT?
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 10, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
Corporal Michael J. Crescenz VA Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Depression is a common psychological disorder seen in 18.5% of Operation Enduring Freedom (OEF), Operation Iraqi Freedom (OIF), and Operation New Dawn (OND) Veterans. Improving the rate of depression recovery and remission is vital to enhance OEF/OIF/OND Veteran's ability to improve work and home adjustment and overall quality of life. OEF/OIF/OND Veterans have reported many barriers to following through with Cognitive therapy skills practice assignments, a key component of CBT therapy, the leading therapy for depression in the VA. Smartphone apps have been identified as a useful widely-used tool to improve the effectiveness of psychological treatments. The investigators propose a full-scale multi-site randomized clinical trial (RCT) to measure the efficacy of CBT-D enhanced with CBT MobileWork-V, a comprehensive CBT skill training smartphone app (the experimental arm) for improving CBT understanding and skill acquisition and depressive symptoms, in OEF/OIF Veterans with depression compared to standard CBT-D.
Detailed Description
Cognitive Behavioral Therapy (CBT) is the leading evidence-based psychotherapy for depression, which affects 18.5% of Operation Enduring Freedom (OEF), Operation Iraqi Freedom (OIF), and Operation New Dawn (OND) Veterans (hereafter referred to as OEF/OIF). Yet, OEF/OIF Veterans had only a 30% average reduction in mean depression scores from the initial to later phase of treatment. This was true despite the rigorous training and certification procedures for VA CBT-D. Improving the rate of depression recovery and remission is vital to enhance OEF/OIF Veteran's ability to improve work and home adjustment and overall quality of life. Broad access to all key ingredients of CBT, including skills practice (homework), is associated with improved and faster recovery from depression. OEF/OIF Veterans and patients with depression have reported many barriers (i.e., time, chaotic lifestyles, and low energy) to following through with their skills practice assignments. In the absence of targeted strategies/interventions to address the barriers that prevent CBT skills practice, OEF/OIF Veterans will remain unable to reap the full benefits/effects of CBT. With specific tailored interventions to address this gap in treatment, OEF/OIF Veterans will improve rates of recovery from depression, diminished home and work adjustment, and poor quality of life. Leveraging the technological savvy of this generation of Veterans to improve access to CBT skills practice is a logical tactic to address this gap in treatment. Smartphone apps have been identified as a useful widely-used tool to improve the effectiveness of psychological treatments. There is, however, a paucity of empirical studies on the use of mobile apps in the treatment of depressed OEF/OIF Veterans and in psychological treatment overall. The promising pilot results of a comprehensive tailored smartphone app for CBT skills practice for OEF/OIF Veterans ("CBT MobileWork-V"), provides initial evidence for a larger-scale randomized clinical trial (RCT) to measure the efficacy of CBT enhanced with CBTMobileWork-V (the experimental arm) for improving CBT understanding and skill acquisition and depressive symptoms, in OEF/OIF Veterans with depression compared to standard CBT-D. Specifically, over a 27-month period the study will randomize 268 eligible OEF/OIF Veterans with depressive symptoms, to either CBT augmented with the comprehensive CBT skill training smartphone app CBT MobileWork-V or standard CBT-D with traditional skills practice methods (i.e., paper and pencil). The Specific Aims of this study are: Primary Aim 1) To assess whether CBT-D augmented with CBT MobileWork-V (hereafter referred to as CBT-D+) promotes greater CBT understanding and skill acquisition compared to traditional CBT-D. Primary Aim 2a) To examine the short-term effect in depressive symptoms after 12 weeks of CBT-D+ versus standard CBT-D. Primary Aim 2b) To examine the long-term effect in depressive symptoms at 6 months post treatment of the CBT-D+ intervention versus traditional CBT-D.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
Depression, OEF/OIF, Mobile Apps, Cognitive Behavioral Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
a full-scale multi-site randomized clinical trial (RCT) to measure the efficacy of CBT-D enhanced with CBT MobileWork-V, a comprehensive CBT skill training smartphone app (the experimental arm) for improving CBT understanding and skill acquisition and depressive symptoms, in OEF/OIF Veterans with depression compared to standard CBT-D.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
268 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CBT-D augmented with CBT MobileWork-V
Arm Type
Experimental
Arm Description
Patients randomized to this condition will receive CBT-D as usual plus access to CBT MobileWork-V, a comprehensive tailored smartphone app for CBT skills practice for OEF/OIF Veterans.
Arm Title
CBT-D
Arm Type
Active Comparator
Arm Description
Patients randomized to CBT-D will receive CBT-D as usual only.
Intervention Type
Behavioral
Intervention Name(s)
CBT MobileWork-V plus CBT
Intervention Description
a smartphone app to assist with CBT homework skills practice plus CBT
Intervention Type
Behavioral
Intervention Name(s)
CBT alone
Other Intervention Name(s)
CBT-D
Intervention Description
CBT therapy individual
Primary Outcome Measure Information:
Title
Skills of Cognitive Therapy (Patient Version) Change
Description
8-item self-report (patient version) and therapist-rated instrument of a 5-point Likert-type scale ranging from (never) to 5 (always or when needed) assesses patients understanding and use of basic CBT skills.
Time Frame
baseline, week 12, and month 9
Secondary Outcome Measure Information:
Title
Patient Health Questionnaire (PHQ-9) Change
Description
9-item questionnaire scoring the DSM-IV criteria for depression as not at all (0) to nearly every day (3); scores of 1 to 4 indicate minimal symptoms while 20 indicates severe depression
Time Frame
baseline and weekly up to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Veteran of OEF/OIF/OND deployments Depressive severity of at least 10 on the PHQ-9 at screening (Patient may also have a DSM-5 56 diagnosis of unipolar Major Depression; PTSD; any anxiety disorder; substance/alcohol abuse; or adjustment disorder) Ability to read at the eighth grade level and to provide informed consent Patients may be taking antidepressants or antianxiety medications where dose has been stable for at least 4 weeks prior to screening evaluation Must have an Android smartphone Must be willing to be audio-taped for fidelity ratings Exclusion Criteria: Diagnoses of schizophrenia, schizo-affective, bipolar, or other psychotic disorder Serious suicidal risk (Patient responds positively to PHQ-9 question #9) See B.3.4.1. Severe PTSD (Score greater than 51 on PTSD Checklist for DSM-5) Severe substance or alcohol dependence (meets DSM-5 criteria of severe)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kathleen M Parks
Phone
(412) 360-2396
Email
Kathleen.Parks@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Elizabeth B Toth, BA
Phone
(412) 954-5382
Email
elizabeth.toth2@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judith Ann Callan, PhD RN
Organizational Affiliation
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington DC VA Medical Center, Washington, DC
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20422-0001
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie Rones
Phone
202-745-4338
Email
julie.rones@va.gov
Facility Name
Jesse Brown VA Medical Center, Chicago, IL
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ashley Taylor, PhD
Phone
312-569-5868
Email
ashley.taylor8@va.gov
Facility Name
Rehabilitation R&D Service, Baltimore, MD
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21202
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Boye, PhD
Phone
410-642-7170
Email
jennifer.boye@va.gov
Facility Name
Minneapolis VA Health Care System, Minneapolis, MN
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417-2309
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Snezana Uresovic, PhD
Phone
612-467-3897
Email
snezana.uresovic@va.gov
Facility Name
Coatesville VA Medical Center, Coatesville, PA
City
Coatesville
State/Province
Pennsylvania
ZIP/Postal Code
19320-2040
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carmella Tress, PhD
Phone
512-823-4666
Email
carmella.tress@va.gov
Facility Name
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4551
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kyong-Mi Chang, MD
Phone
215-823-5800
Ext
5893
Email
Kyong-Mi.Chang@va.gov
First Name & Middle Initial & Last Name & Degree
Lisa Dorman
Phone
2158235800
Ext
6024
Email
lisa.dorman@va.gov
Facility Name
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15240
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kathleen M Parks
Phone
(412) 360-2396
Email
Kathleen.Parks@va.gov
First Name & Middle Initial & Last Name & Degree
Judith Ann Callan, PhD RN
Facility Name
VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX
City
Dallas
State/Province
Texas
ZIP/Postal Code
75216-7167
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Justin Litvin, PhD
Phone
817-730-0106
Email
justin.litvin@va.gov
Facility Name
Clement J. Zablocki VA Medical Center, Milwaukee, WI
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53295-0001
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christina M Hove, PhD
Phone
414-384-2000
Email
mary.hove@va.gov

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Does Adding a Tailored Cognitive Behavioral Therapy (CBT) Mobile Skills App Mediate Rates of Depression

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