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Completed

NCT Number: NCT02658669

Cognitive-Behavioral Therapy for Veterans With TBI

Many Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn era Veterans have suffered a mild traumatic brain injury (mTBI), and now cope with multiple post-injury symptoms, including sleep disturbances (especially insomnia). Chronic insomnia in mTBI patients has the potential to exacerbate other symptoms, delay recovery, and negatively affect many of the cognitive, psychological, and neuromuscular sequelae of mTBI, thereby decreasing quality of life. Although Cognitive-Behavioral Therapy for Insomnia (CBT-I) has been shown to be an effective evidence-based treatment for insomnia, there are no published randomized controlled trials evaluating the potential strengths and/or limitations of CBT-I in post-mTBI patients. Therefore, assessing CBT-I in the context of mTBI holds promise to provide substantial benefits in terms of improved rehabilitation outcomes in Veterans who have suffered mTBI.

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Key information

About this study

This VA Rehabilitation Research and Development Career Development Award (CDA-2) proposal is designed to significantly advance the application of Behavioral Sleep Medicine practices in the treatment of Veterans seen in the VA Healthcare System, especially those recovering from traumatic brain injury (TBI). TBI has been deemed the "signature wound" of the Iraq and Afghanistan Wars, occurring in about 19.5% of Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn (OEF/OIF/OND) service members. For many Veterans, mild traumatic brain injury (mTBI) can be associated with persistent post-concussive symptoms, especially sleep disturbances. Sleep disturbances are among the most frequent complaints following mTBI, with studies suggesting that over 93% of Veterans who experienced brain injuries develop chronic sleep problems. Of the sleep disturbances diagnosed in this patient population the most common is insomnia, observed in over 50% of patients. Chronic and untreated insomnia is known to be associated with and/or increase risk for psychiatric problems, suicidal ideation, and unhealthy lifestyles (e.g., alcohol/drug abuse), lead to poorer physical health, disruption in major social and occupational responsibilities, and decreased quality of life, and may generally contribute to the persistence of post-concussive symptoms beyond the expected period of recovery. As such, treatment of sleep disturbance represents an essential component of Veteran care, one which may be particularly beneficial for Veterans with history of mTBI who commonly present to the clinic with complex multi-symptom concerns.

To address this important clinical issue, the proposed randomized clinical trial (RCT) will attempt to assess the efficacy of Cognitive-Behavioral Therapy for Insomnia (CBT-I) versus a Sleep Education control in Veterans with insomnia and a history of mTBI. CBT-I is recommended by the American Academy of Sleep Medicine for treatment of chronic insomnia and has also been adopted by the VA within an Evidence Based Practice roll-out program. Despite the acceptance of CBT-I as a first line treatment for sleep disturbance, there are no published RCTs evaluating CBT-I in mTBI patient populations. Therefore, this proposed investigation will address this gap in the literature by assessing the efficacy of CBT-I in Veterans with history of head injury.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • OEF/OIF/OND Veteran ages 18-55.
  • Documented history of mild TBI (documented in the medical record and where possible from the VA TBI second-level evaluation)
  • Loss of consciousness 30 minutes
  • Post-traumatic amnesia 1 day
  • At least 3 months post-TBI.
  • A diagnosis of insomnia classified as:
  • Diagnostic and Statistical Manual of Mental Disorders-5 (DSM 5) criteria that include: trouble falling asleep, staying asleep, waking too early, and/or non-restorative sleep with accompanied daytime impairment in functioning for > 3 months, occurring at least 3 nights per week.
  • Subjective sleep disturbance defined by a Pittsburgh Sleep Quality Index score >5 and Insomnia Severity Index score >7 at intake.
  • No prior exposure to and/or treatment with CBT-I within the past 2 years.
  • Must be stable on medication regimen for at least 1 month prior to enrollment in study.

Exclusion criteria

  • History of a neurological disorder (besides TBI), dementia, or premorbid IQ <70.
  • Schizophrenia, psychotic disorder, and/or bipolar disorder.
  • Evidence of suicidality more than "low risk" as determined by the VA Comprehensive Suicide Risk Assessment (CSRA).
  • Sleep disturbances other than insomnia (e.g., untreated obstructive sleep apnea and/or periodic limb movements)
  • Alcohol and/or substance abuse within the past 30 days.

Treatment and study plan

Cognitive-Behavioral Therapy for Insomnia

Behavioral

Intervention includes strategies designed to improve sleep such as: sleep restriction, stimulus-control techniques, sleep hygiene education, and relaxation training.

Other names: CBT-I

Sleep Education

Behavioral

Intervention includes sleep hygiene education and education regarding the impact of TBI on sleep.

Primary outcomes

  1. Change in Insomnia Severity

    Time frame: Pre-Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in insomnia severity. Scale used is Insomnia Severity Index (ISI). Minimum value= 0; maximum value = 28. Lower score equals better outcome.

Secondary outcomes

  1. Change in Depressive Symptomatology

    Time frame: Pre-Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in depressive symptoms assessed using the Patient Health Questionnaire-9 (PHQ-9) a self-report measure of depression. Minimum value = 0; maximum value = 27. Lower scores indicate fewer depressive symptoms.

  2. Change in PTSD Stressor Specific Checklist 5

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in PTSD symptoms assessed using the PTSD Stressor Specific Checklist 5 (PCL-5) a self-report measure of PTSD. Minimum score = 0, maximum score = 80. Lower scores indicate less PTSD symptomatology.

  3. Change in World Health Organization Disability Assessment Scale-2

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in global functioning and disability will be assessed using the World Health Organization Disability Assessment Scale-2, a self-report measure. Minimum value = 0; maximum value = 100. Lower scores indicates less disability.

  4. Change in Pittsburgh Sleep Quality Index

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in sleep quality will be assessed with the Pittsburgh Sleep Quality Index (PSQI). Minimum value = 0; maximum value= 21. Lower score indicates less general sleep disturbance.

Other outcomes

  1. Change in Patient Reported Outcomes Measurement Information System (PROMIS) Pain

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in pain will be assessed using the Patient Reported Outcomes Measurement Information System (PROMIS) pain assessment, as self-report measure of pain. Measures are scored on a T-score (mean=50, SD=10) Minimum score = <20 ; maximum score = >80. Lower scores indicate less pain interference in daily life.

  2. Change in Neuropsychological Functioning: Attention/Processing Speed

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in cognitive functioning will be evaluated through standardized assessments of attention and processing speed. The tasks that will be administered include: the Wechsler Adult Intelligence Scale Fourth Edition (WAIS-IV) Digit Symbol and Symbol Search to measure attention and processing speed. WAIS-IV raw minimum value score=45; maximum score=155. Scaled score used: minimum score = 1; maximum score = 19. Higher score equals a better outcome.

  3. Change In Neuropsychological Functioning: Verbal Learning and Memory

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in cognitive functioning will be evaluated through standardized assessments of verbal learning and memory. The Hopkins Verbal Learning Test-Revised (HVLT-R) was used to measure learning and memory, and was measured by "Total Recall" score and "Delayed Recall" score. HVLT Total Recall raw scores minimum value=0; maximum value=36. Measures scored on a T-Score; minimum t-score score:0, maximum t-score >80. Higher t-scores indicate better outcome. HVLT delayed recall minimum raw score value=0; maximum value=12. Measures scored on a T-Score; maximum t-score value: 60, minimum =0. Higher t-scores indicate better outcome. Population mean and standard deviation calculated based on age. Mean age of the population was 36 years = total recall population t score mean: 28.04, SD: 4.43. Delayed recall population t score mean: 9.92, SD: 2.04.

  4. Change In Neuropsychological Functioning: Executive Functioning

    Time frame: Pre- Treatment (0-weeks), Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in cognitive functioning will be evaluated through standardized assessments of executive functioning. The Delis-Kaplan Executive Function Scale (D-KEFS) Trials and Color-Word Tasks was used to measure executive functioning, as measured by Color-Word Inhibition, Color-Word Switching Inhibition, and Trails. Scored using a scaled-score (minimum=1, maximum=19 for all measures). Higher scores indicate better outcome.

  5. Change in Sleep Efficiency as Measured by Polysomnography

    Time frame: Pre-Treatment (0-weeks),Post-Treatment (8-weeks), Follow-Up (12-weeks)

    Change in sleep efficiency will be assessed through overnight polysomnographic sleep studies.

Sponsors and collaborators

Lead sponsor

VA Office of Research and Development

Fed

Registry information

Official study title

Cognitive Behavioral Therapy for Insomnia for Veterans With History of TBI

Important dates

Study start
2016
Primary completion
2022
Study completion
2022
First posted
Jan 20, 2016
Registry last updated
Sep 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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