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Sleep and Pain Intervention for Chronic Insomnia Using Virtual Reality Pilot Study (iVR)

Primary Purpose

Insomnia Chronic, Pain, Chronic

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Virtual Reality Mediated Relaxation
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia Chronic focused on measuring Sleep, Pain, Virtual Reality

Eligibility Criteria

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

General inclusion criteria:

  1. 18+ years,
  2. able to read and understand English,
  3. pain and insomnia complaints for 6+ months,
  4. diagnosed with (4.1) insomnia based on the criteria below:

4.1) insomnia complaints for 6+ months that:

4.1a) occur despite adequate opportunity and circumstances for sleep, and

4.1b) consist of 1 or more of the following: difficulty falling asleep, staying asleep, waking up too early, nonrestorative sleep,

4.1c) daytime dysfunction (mood, cognitive, social, occupational) due to insomnia,

4.1d) screening ISI score ≥ 11

Exclusion criteria:

  1. unable to provide informed consent,
  2. unable to complete forms and implement treatment due to cognitive impairment (MMSE<26),
  3. sleep disorder other than insomnia (i.e., sleep apnea [apnea/hypopnea index, AHI>15], Periodic Limb Movement Disorder-PLMD [myoclonus arousals per hour > 15]),
  4. bipolar or seizure disorder (due to risk of sleep restriction treatment),
  5. other major psychopathology except depression or anxiety (e.g., suicidal ideation/intent, psychotic disorders),
  6. severe untreated psychiatric comorbidity,
  7. psychotropic or other medications (e.g., beta-blockers) that alter pain or sleep,
  8. participation in any nonpharmacological treatment (including CBT) for pain, sleep, fatigue or mood outside the current study

Sites / Locations

  • University of MissouriRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Virtual Reality Based Relaxation Therapy

Arm Description

This is a pilot trial with one treatment condition (VR mediation).

Outcomes

Primary Outcome Measures

Daily Electronic Sleep/Pain Diaries
Daily electronic dairies will record pain intensity and unpleasantness, sleep (latency, wake after onset, efficiency, quality), fatigue, sleep and pain medication consumption
Objective Daily Sleep Actiwatch-2 (Wake After Sleep Onset)
Objective wake after sleep onset
Objective Daily Sleep Actiwatch-2 (Sleep Onset Latency)
Objective sleep onset latency
Objective Daily Sleep Actiwatch-2 (Sleep Efficiency)
Objective sleep efficiency
Insomnia Severity Index
Insomnia severity measurement; min: 0 max:28; higher score means greater insomnia severity
Fatigue Severity Scale
Fatigue severity; min:10 max: 73; higher score means higher fatigue severity

Secondary Outcome Measures

Patient centered outcomes questionnaire
The Patient Centered Outcomes questionnaire assesses four domains (pain, fatigue, emotional distress, and interference with daily activities) relevant to chronic pain populations on a numerical rating scale ranging from 0-10; min: 0 max:200; 200; A greater score equates a worse outcome
Computerized Cognitive Assessments -WCST
Determine level of cognitive functioning
Computerized Cognitive Assessments - Stroop Task
Determine level of cognitive functioning
Computerized Cognitive Assessments - Sternberg tasks
Determine level of cognitive functioning
List learning-Rey Auditory Learning Test modified for visual presentation
Immediate and delayed recall memory
Beck Depression Inventory Second Edition
Depressive symptom assessment; min: 0 max: 63; Higher score means higher severity of depression
State Trait Anxiety Inventory
Assessment of Anxiety symptoms; mix: 0 max:60; higher score means higher anxiety
Cognitive Failures Questionnaire
Self-reported failures in perception, memory, and motor function; min:0 max: 100; higher score means greater cognitive failure

Full Information

First Posted
January 16, 2020
Last Updated
December 9, 2021
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT04253691
Brief Title
Sleep and Pain Intervention for Chronic Insomnia Using Virtual Reality Pilot Study
Acronym
iVR
Official Title
Sleep and Pain Intervention for Chronic Insomnia Using Virtual Reality Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
February 9, 2020 (Actual)
Primary Completion Date
January 2025 (Anticipated)
Study Completion Date
January 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri-Columbia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes

5. Study Description

Brief Summary
Sleep disturbances are common among chronic pain patients, with reports typically ranging from 50-70% of patients reporting sleep difficulties. It is well documented that, alongside a high comorbidity with chronic pain, chronic insomnia also has high comorbidity with, and is a risk factor for, developing an anxiety disorders. This clinical trial will examine the effects of virtual reality (VR) meditation environments on patients with pain- and insomnia-related anxiety. The purpose of this study is to examine the benefits of using VR meditation with patients with chronic pain and chronic sleep disturbance so that clinicians can more effectively treat core causes to symptoms and reduce counterproductive therapies. Research objectives include: To examine the clinical and health characteristics, including sleep, pain, fatigue, cognitive abilities, and cardiovascular health in patients with chronic pain. To examine changes in the primary clinical outcomes, including chronic pain, complaints of poor sleep, and fatigue. To examine changes in the secondary clinical outcomes, including mood, daytime functioning, cognitive functioning, and cardiovascular health. To examine the mechanistic variables, including arousal (heart rate variability, HRV) and CS (thermal response).
Detailed Description
Sleep disturbances are common among chronic pain patients, with reports typically ranging from 50-70% of patients reporting sleep difficulties. It is well documented that, alongside a high comorbidity with chronic pain, chronic insomnia also has high comorbidity with, and is a risk factor for, developing an anxiety disorders. Research has shown that Cognitive Behavioral Therapies (CBT) are efficacious in treating patient with comorbid insomnia and chronic pain (e.g., improvements in sleep parameters, normal sleep efficiency, reductions in pain severity. CBT addresses a number of factors involved in the maintenance of patient sleep and health issues, and a key piece of CBT for insomnia and pain is the reduction of worrisome thoughts, or anxiety related to sleep and pain issues. A common evidence-based strategy used for reducing anxiety and worry is the practice of relaxation. The aim of this study is to investigate the benefits of replacing treatment as usual (TAU) relaxation practices, with Virtual Reality (VR) mediation environments within CBT treatment. Virtual Reality Meditation for Anxiety There are few studies in the literature demonstrating a relationship between Virtual Reality (VR) - a computer generated environment that presents the user with a realistic three-dimensional space - and reductions in anxious symptomology. However, the results of those studies are very encouraging. In a case study, Tarrant and Cope treated 4 firefighters who had anxiety and anxiety-based disorders with a Positivity VR Experience. 3 of 4 treated patients exhibited increased left gamma symmetry, associated with approach behavior and increased mood, and 3 of 4 patients showed increases in State-Cheerfulness and Positive Affect. Tarrant and colleagues also conducted a pilot study, where they treated 14 patients who had moderate or higher levels of generalized anxiety with a 5-minute Mindfulness in Nature experience. Patients in the VR meditation group showed both global and regional decreases in Beta activity (i.e., decrease in frequencies associated with qualitatively anxious states and decreased self-reported State Anxiety. Overall, these results seem promising, as they provide preliminary evidence supporting that VR interventions may be a useful and effective tool for the treatment of elevated anxiety symptoms. In summary, this clinical trial will examine the effects of VR meditation environments on patients with pain- and insomnia-related anxiety. The proposed study design will yield important information about the efficacy of VR meditation practices. The purpose of this study is to examine the benefits of using VR meditation with patients with chronic pain and chronic sleep disturbance so that clinicians can more effectively treat core causes to symptoms and reduce counterproductive therapies. Ultimately, this research targets two important public health concerns, namely insomnia and chronic pain. Insomnia in the context of chronic pain has been relatively understudied. Thus, the results of the present study will provide unique insights into sleep and chronic pain and will advance knowledge in the fields of both sleep and pain. Although the results of this study will be specific to chronic pain patients, they will have broader implications for other medical populations likely to suffer from chronic pain and insomnia (i.e., cancer patients, older adults). The information gained has the potential to make a significant contribution to behavioral healthcare practices for a wide variety of disorders, not just insomnia and pain. Thus, this research has implications not only for future sleep and pain research but also for other types of treatment-related research. 2. Objectives To examine the clinical and health characteristics, including sleep, pain, fatigue, cognitive abilities, and cardiovascular health in patients with chronic pain. To examine changes in the primary clinical outcomes, including chronic pain, complaints of poor sleep, and fatigue. To examine changes in the secondary clinical outcomes, including mood, daytime functioning, cognitive functioning, and cardiovascular health. To examine the mechanistic variables, including arousal (heart rate variability, HRV) and CS (thermal response).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia Chronic, Pain, Chronic
Keywords
Sleep, Pain, Virtual Reality

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual Reality Based Relaxation Therapy
Arm Type
Experimental
Arm Description
This is a pilot trial with one treatment condition (VR mediation).
Intervention Type
Device
Intervention Name(s)
Virtual Reality Mediated Relaxation
Intervention Description
Participants will use a brief Virtual Reality relaxation protocol to improve their insomnia. Their workbook will contain a handout that outlines the details. Participants will be encouraged to refer to it at home if they forget any part of the procedure.
Primary Outcome Measure Information:
Title
Daily Electronic Sleep/Pain Diaries
Description
Daily electronic dairies will record pain intensity and unpleasantness, sleep (latency, wake after onset, efficiency, quality), fatigue, sleep and pain medication consumption
Time Frame
6 weeks
Title
Objective Daily Sleep Actiwatch-2 (Wake After Sleep Onset)
Description
Objective wake after sleep onset
Time Frame
6 weeks
Title
Objective Daily Sleep Actiwatch-2 (Sleep Onset Latency)
Description
Objective sleep onset latency
Time Frame
6 weeks
Title
Objective Daily Sleep Actiwatch-2 (Sleep Efficiency)
Description
Objective sleep efficiency
Time Frame
6 weeks
Title
Insomnia Severity Index
Description
Insomnia severity measurement; min: 0 max:28; higher score means greater insomnia severity
Time Frame
6 weeks
Title
Fatigue Severity Scale
Description
Fatigue severity; min:10 max: 73; higher score means higher fatigue severity
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Patient centered outcomes questionnaire
Description
The Patient Centered Outcomes questionnaire assesses four domains (pain, fatigue, emotional distress, and interference with daily activities) relevant to chronic pain populations on a numerical rating scale ranging from 0-10; min: 0 max:200; 200; A greater score equates a worse outcome
Time Frame
6 weeks
Title
Computerized Cognitive Assessments -WCST
Description
Determine level of cognitive functioning
Time Frame
6 weeks
Title
Computerized Cognitive Assessments - Stroop Task
Description
Determine level of cognitive functioning
Time Frame
6 weeks
Title
Computerized Cognitive Assessments - Sternberg tasks
Description
Determine level of cognitive functioning
Time Frame
6 weeks
Title
List learning-Rey Auditory Learning Test modified for visual presentation
Description
Immediate and delayed recall memory
Time Frame
6 weeks
Title
Beck Depression Inventory Second Edition
Description
Depressive symptom assessment; min: 0 max: 63; Higher score means higher severity of depression
Time Frame
6 weeks
Title
State Trait Anxiety Inventory
Description
Assessment of Anxiety symptoms; mix: 0 max:60; higher score means higher anxiety
Time Frame
6 weeks
Title
Cognitive Failures Questionnaire
Description
Self-reported failures in perception, memory, and motor function; min:0 max: 100; higher score means greater cognitive failure
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
General inclusion criteria: 18+ years, able to read and understand English, pain and insomnia complaints for 6+ months, diagnosed with (4.1) insomnia based on the criteria below: 4.1) insomnia complaints for 6+ months that: 4.1a) occur despite adequate opportunity and circumstances for sleep, and 4.1b) consist of 1 or more of the following: difficulty falling asleep, staying asleep, waking up too early, nonrestorative sleep, 4.1c) daytime dysfunction (mood, cognitive, social, occupational) due to insomnia, 4.1d) screening ISI score ≥ 11 Exclusion criteria: unable to provide informed consent, unable to complete forms and implement treatment due to cognitive impairment (MMSE<26), sleep disorder other than insomnia (i.e., sleep apnea [apnea/hypopnea index, AHI>15], Periodic Limb Movement Disorder-PLMD [myoclonus arousals per hour > 15]), bipolar or seizure disorder (due to risk of sleep restriction treatment), other major psychopathology except depression or anxiety (e.g., suicidal ideation/intent, psychotic disorders), severe untreated psychiatric comorbidity, psychotropic or other medications (e.g., beta-blockers) that alter pain or sleep, participation in any nonpharmacological treatment (including CBT) for pain, sleep, fatigue or mood outside the current study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christina S McCrae, PhD
Phone
573-882-0982
Email
mccraec@health.missouri.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Angelynn Simenson, MS
Email
aps455@health.missouri.edu
Facility Information:
Facility Name
University of Missouri
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Riley Stephens

12. IPD Sharing Statement

Citations:
PubMed Identifier
30087642
Citation
Tarrant J, Viczko J, Cope H. Virtual Reality for Anxiety Reduction Demonstrated by Quantitative EEG: A Pilot Study. Front Psychol. 2018 Jul 24;9:1280. doi: 10.3389/fpsyg.2018.01280. eCollection 2018.
Results Reference
background
Citation
Thompson, M., & Thompson, L. (2007). Neurofeedback for stress management. Principles and practice of stress management, 3, 249-287.
Results Reference
background
Citation
Tarrant, J., & Cope, H. (2018). Combining frontal gamma asymmetry neurofeedback with virtual reality: A proof-of-concept case study. NeuroRegulation, 5(2), 57-66. https://doi.org/10.15540/nr.5.2.57
Results Reference
background
Citation
Sutton, S. K., & Davidson, R. J. (1997). Prefrontal Brain Asymmetry: A Biological Substrate of the Behavioral Approach and Inhibition Systems. Psychological Science, 8(3), 204-210. https://doi.org/10.1111/j.1467-9280.1997.tb00413.x
Results Reference
background
Citation
Price, J., & Budzynski, T. (2009). Anxiety, EEG patterns, and neurofeedback. Introduction to quantitative EEG and neurofeedback: Advanced theory and applications, 453-470.
Results Reference
background

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Sleep and Pain Intervention for Chronic Insomnia Using Virtual Reality Pilot Study

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