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CBT-I for Psychosis: Guidelines, Preliminary Efficacy, and Functional Outcomes (CBT-I)

Primary Purpose

Insomnia, Psychosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive Behavioral Therapy-Insomnia
Health and Wellness
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 Insomnia focused on measuring Schizophrenia and Disorders with Psychotic Feature, Mental Disorders, Insomnia Disorder

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnostic and Statistical Manual of Disorders, 5th edition (DSM 5) diagnosis of schizophrenic disorders (295.0-295.9), affective psychoses (296.0-296.1, 296.4-296.8), or major depression with psychotic features (296.24, 296.34).
  2. Self-reported symptoms of insomnia via an Insomnia Severity Index (ISI) score of 15 or greater.
  3. Age between 18 and 80 as determined by medical record review.
  4. Participation in outpatient mental health services at a designated study site.
  5. Sufficient clinical stability to participate as deemed by a treatment provider.
  6. Capacity to sign Informed Consent.

Exclusion Criteria:

  1. Current problematic drug or alcohol use that impacts functioning and study engagement, as deemed by a treatment provider.
  2. Currently in CBT-I treatment, determined by medical records.
  3. Positive screen for sleep apnea via a portable sleep apnea screening device or a prior diagnosis of sleep apnea in medical records.

Sites / Locations

  • Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Cognitive Behavioral Therapy-Insomnia

Health and Wellness

Arm Description

CBT-I addresses cognitive, arousal and behavioral factors related to sleep difficulties. Sessions combine assessment, conceptualization, psychoeducation, behavioral strategies and cognitive therapy, using a consistent structure including review of participants' sleep log and adherence to behavioral guidelines, modification of time in bed, cognitive therapy, and relaxation techniques. CBT-I also incorporates psychoeducation about biological and psychological elements that regulate sleep. Other strategies include stimulus control (i.e., getting out of bed when not sleepy) to extinguish the conditioned arousal common in insomnia, and relaxation techniques to reduce arousal associated with the bed, bedroom, or bedtime.

Health and Wellness is a general self-management curriculum focused on providing education and support for managing physical and emotional well-being. Each session follows a basic structure including review of previous session material, new educational information and discussion on several topics over the course of single or multiple sessions. Each session will focus on the impact of the topic on overall health and wellness, identifying benefits and challenges to improving or maintaining health in that area, and strategies that clients may find helpful to address challenges in that area. Example topics include physical activity/exercise, nutrition/healthy eating, managing medications and side effects, and addictive behaviors (e.g., substance use, gambling, eating).

Outcomes

Primary Outcome Measures

Insomnia Severity Index (ISI)
ISI score; scored on a scale of 0 to 28, with higher scores indicating worse insomnia severity.

Secondary Outcome Measures

Insomnia Severity Index (ISI)
ISI score; scored on a scale of 0 to 28, with higher scores indicating worse insomnia severity.
Veterans RAND 36-Item Health Survey Mental Component Score
Veterans RAND 36-Item Health Survey score Mental Component Score; Possible scores range from 0 to 100, with higher scores indicating greater mental quality of life.
Veterans RAND 36-Item Health Survey Mental Component Score
Veterans RAND 36-Item Health Survey Mental Component Score; Possible scores range from 0 to 100, with higher scores indicating greater mental health quality of life.
World Health Organization Disability Assessment Schedule (WHO-DAS), Participation in Society Subscale
WHO-DAS score; scores range from 0 to 100 where 100 is full disability.
World Health Organization Disability Assessment Schedule (WHO-DAS), Participation in Society Subscale
WHO-DAS score; scores range from 0 to 100 where 100 is full disability.

Full Information

First Posted
August 26, 2015
Last Updated
February 15, 2023
Sponsor
VA Office of Research and Development
Collaborators
VA Maryland Health Care System
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1. Study Identification

Unique Protocol Identification Number
NCT02535923
Brief Title
CBT-I for Psychosis: Guidelines, Preliminary Efficacy, and Functional Outcomes
Acronym
CBT-I
Official Title
CBT-I for Psychosis: Guidelines, Preliminary Efficacy, and Functional Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
April 20, 2021 (Actual)
Study Completion Date
April 20, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
VA Maryland Health Care System

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
No

5. Study Description

Brief Summary
The goal of this project is to develop guidelines for the clinical tailoring of Cognitive Behavioral Therapy for Insomnia (CBT-I) for Veterans with psychotic disorders and insomnia, and to test the acceptability, feasibility, and preliminary efficacy of CBT-I for improving sleep-related functional outcomes in this population.
Detailed Description
The goal of this project is to develop guidelines for the clinical tailoring of Cognitive Behavioral Therapy for Insomnia (CBT-I) for Veterans with psychotic disorders and insomnia, and to test the acceptability, feasibility, and preliminary efficacy of CBT-I for improving sleep-related functional outcomes in this population. Specific Aim 1: Develop empirically-derived guidelines for the clinical tailoring of CBT-I materials and procedures for Veterans with psychotic disorders through an iterative process with input from Veteran clients, CBT-I experts and providers, as well as those with expertise in psychotic disorders. Specific Aim 2: Establish the acceptability of CBT-I for Veterans with psychotic disorders and insomnia when delivered using guidelines developed in Specific Aim 1 in order to make further refinements to the guidelines in a preliminary trial with 6 Veterans with psychosis and insomnia. Specific Aim 3: Conduct a randomized controlled trial (n=60) to test the feasibility and preliminary efficacy of CBT-I in producing positive changes at post-treatment and 3-month follow-up on the outcomes of insomnia symptoms, sleep quality, and functioning.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia, Psychosis
Keywords
Schizophrenia and Disorders with Psychotic Feature, Mental Disorders, Insomnia Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Behavioral Therapy-Insomnia
Arm Type
Experimental
Arm Description
CBT-I addresses cognitive, arousal and behavioral factors related to sleep difficulties. Sessions combine assessment, conceptualization, psychoeducation, behavioral strategies and cognitive therapy, using a consistent structure including review of participants' sleep log and adherence to behavioral guidelines, modification of time in bed, cognitive therapy, and relaxation techniques. CBT-I also incorporates psychoeducation about biological and psychological elements that regulate sleep. Other strategies include stimulus control (i.e., getting out of bed when not sleepy) to extinguish the conditioned arousal common in insomnia, and relaxation techniques to reduce arousal associated with the bed, bedroom, or bedtime.
Arm Title
Health and Wellness
Arm Type
Active Comparator
Arm Description
Health and Wellness is a general self-management curriculum focused on providing education and support for managing physical and emotional well-being. Each session follows a basic structure including review of previous session material, new educational information and discussion on several topics over the course of single or multiple sessions. Each session will focus on the impact of the topic on overall health and wellness, identifying benefits and challenges to improving or maintaining health in that area, and strategies that clients may find helpful to address challenges in that area. Example topics include physical activity/exercise, nutrition/healthy eating, managing medications and side effects, and addictive behaviors (e.g., substance use, gambling, eating).
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral Therapy-Insomnia
Intervention Description
CBT-I addresses cognitive, arousal and behavioral factors related to sleep difficulties. Sessions combine assessment, conceptualization, psychoeducation, behavioral strategies and cognitive therapy, using a consistent structure including review of participants' sleep log and adherence to behavioral guidelines, modification of time in bed, cognitive therapy, and relaxation techniques. CBT-I also incorporates psychoeducation about biological and psychological elements that regulate sleep. Other strategies include stimulus control (i.e., getting out of bed when not sleepy) to extinguish the conditioned arousal common in insomnia, and relaxation techniques to reduce arousal associated with the bed, bedroom, or bedtime.
Intervention Type
Behavioral
Intervention Name(s)
Health and Wellness
Intervention Description
Health and Wellness is a general self-management curriculum focused on providing education and support for managing physical and emotional well-being. Each session follows a basic structure including review of previous session material, new educational information and discussion on several topics over the course of single or multiple sessions. Each session will focus on the impact of the topic on overall health and wellness, identifying benefits and challenges to improving or maintaining health in that area, and strategies that clients may find helpful to address challenges in that area. Example topics include physical activity/exercise, nutrition/healthy eating, managing medications and side effects, and addictive behaviors (e.g., substance use, gambling, eating).
Primary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
ISI score; scored on a scale of 0 to 28, with higher scores indicating worse insomnia severity.
Time Frame
Participants will be assessed following completion of the study intervention, an expected average of 10 weeks.
Secondary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
ISI score; scored on a scale of 0 to 28, with higher scores indicating worse insomnia severity.
Time Frame
Participants will be assessed a second time following completion of the study intervention, an expected average of 22 weeks.
Title
Veterans RAND 36-Item Health Survey Mental Component Score
Description
Veterans RAND 36-Item Health Survey score Mental Component Score; Possible scores range from 0 to 100, with higher scores indicating greater mental quality of life.
Time Frame
Participants will be assessed following completion of the study intervention, an expected average of 10 weeks.
Title
Veterans RAND 36-Item Health Survey Mental Component Score
Description
Veterans RAND 36-Item Health Survey Mental Component Score; Possible scores range from 0 to 100, with higher scores indicating greater mental health quality of life.
Time Frame
Participants will be assessed a second time following completion of the study intervention, an expected average of 22 weeks.
Title
World Health Organization Disability Assessment Schedule (WHO-DAS), Participation in Society Subscale
Description
WHO-DAS score; scores range from 0 to 100 where 100 is full disability.
Time Frame
Participants will be assessed following completion of the study intervention, an expected average of 10 weeks.
Title
World Health Organization Disability Assessment Schedule (WHO-DAS), Participation in Society Subscale
Description
WHO-DAS score; scores range from 0 to 100 where 100 is full disability.
Time Frame
Participants will be assessed a second time following completion of study intervention, an estimated average of 22 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnostic and Statistical Manual of Disorders, 5th edition (DSM 5) diagnosis of schizophrenic disorders (295.0-295.9), affective psychoses (296.0-296.1, 296.4-296.8), or major depression with psychotic features (296.24, 296.34). Self-reported symptoms of insomnia via an Insomnia Severity Index (ISI) score of 15 or greater. Age between 18 and 80 as determined by medical record review. Participation in outpatient mental health services at a designated study site. Sufficient clinical stability to participate as deemed by a treatment provider. Capacity to sign Informed Consent. Exclusion Criteria: Current problematic drug or alcohol use that impacts functioning and study engagement, as deemed by a treatment provider. Currently in CBT-I treatment, determined by medical records. Positive screen for sleep apnea via a portable sleep apnea screening device or a prior diagnosis of sleep apnea in medical records.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth A. Klingaman, PhD
Organizational Affiliation
Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18840034
Citation
Cohrs S. Sleep disturbances in patients with schizophrenia : impact and effect of antipsychotics. CNS Drugs. 2008;22(11):939-62. doi: 10.2165/00023210-200822110-00004.
Results Reference
background
PubMed Identifier
24005883
Citation
Bramoweth AD, Germain A. Deployment-related insomnia in military personnel and veterans. Curr Psychiatry Rep. 2013 Oct;15(10):401. doi: 10.1007/s11920-013-0401-4.
Results Reference
background
PubMed Identifier
26279058
Citation
Klingaman EA, Palmer-Bacon J, Bennett ME, Rowland LM. Sleep Disorders Among People With Schizophrenia: Emerging Research. Curr Psychiatry Rep. 2015 Oct;17(10):79. doi: 10.1007/s11920-015-0616-7.
Results Reference
background
PubMed Identifier
23423416
Citation
Buysse DJ. Insomnia. JAMA. 2013 Feb 20;309(7):706-16. doi: 10.1001/jama.2013.193.
Results Reference
background
PubMed Identifier
16448292
Citation
Irwin MR, Cole JC, Nicassio PM. Comparative meta-analysis of behavioral interventions for insomnia and their efficacy in middle-aged adults and in older adults 55+ years of age. Health Psychol. 2006 Jan;25(1):3-14. doi: 10.1037/0278-6133.25.1.3.
Results Reference
background
PubMed Identifier
21367359
Citation
Myers E, Startup H, Freeman D. Cognitive behavioural treatment of insomnia in individuals with persistent persecutory delusions: a pilot trial. J Behav Ther Exp Psychiatry. 2011 Sep;42(3):330-6. doi: 10.1016/j.jbtep.2011.02.004. Epub 2011 Mar 2.
Results Reference
background
PubMed Identifier
14982330
Citation
Dopke CA, Lehner RK, Wells AM. Cognitive-behavioral group therapy for insomnia in individuals with serious mental illnesses: a preliminary evaluation. Psychiatr Rehabil J. 2004 Winter;27(3):235-42. doi: 10.2975/27.2004.235.242.
Results Reference
background

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CBT-I for Psychosis: Guidelines, Preliminary Efficacy, and Functional Outcomes

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