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OpenTrials
Completed

NCT Number: NCT04236284

Management of Chronic Pain and PTSD in Gulf War Veterans With tDCS+Prolonged Exposure

Gulf War Veterans (a DoD/VA defined service era corresponding to the first Gulf War under operations Desert Storm and Desert Shield 1990-1991), especially those who present with Post-Traumatic Stress Disorder (PTSD), are particularly likely to experience chronic pain. Veterans with co-morbid chronic pain and PTSD utilize healthcare services at a higher rate than those with pain or PTSD alone. Unfortunately, there are no integrated treatments for Pain and PTSD. Moreover, non-pharmacological treatments for pain such as Cognitive Behavioral Therapy are useful in only about 50% of cases. Transcranial direct current stimulation (tDCS) may be an effective treatment for pain, and has been recently used to ameliorate PTSD symptoms. Prolonged Exposure Therapy (PE) is highly effective in treating PTSD symptoms. Therefore, we propose to (a) integrate & (b) gather feasibility data for home-based tDCS + PE for Pain and PTSD with 15 Gulf War Veterans.

The Overall Aim of the present proposal is to integrate, refine and investigate the feasibility (e.g., pilot testing, recruitment, attrition, assessment) of tDCS for treating chronic pain with a best practices evidence-based treatment for PTSD (i.e., Prolonged Exposure: PE) in 15 Gulf War veterans, a group for which both pain (fibromyalgia) and PTSD are particularly problematic.

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Key information

Conditions

Chronic Pain Mental Disorders Neurologic Manifestations PTSD Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms Stress Disorders, Post-Traumatic Stress Disorders, Traumatic Trauma and Stressor Related Disorders

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Texas Health Science Center at Houston

Houston, Texas, 77030, United States

About this study

Chronic pain is one of the most prevalent health conditions among Americans, affecting about a third of the general population. In Gulf War (1990-1991) veterans, chronic pain is even more common, with a prevalence of about 50%. Indeed, the pain-related fibromyalgia diagnosis is part of Gulf War Syndrome and is highly comorbid with other common military service-related health problems such as Posttraumatic Stress Disorder (PTSD). Moreover, lack of effective, integrated, and available alternative treatments for chronic pain contributes to the opioid epidemic.

PTSD is also highly prevalent in Gulf War Veterans, at about 15-25% of Operation Desert Shield and Desert Storm Veterans. Moreover, several investigators note that PTSD treatment response is poorer for Veterans who experience chronic pain and for Veterans who served in the Gulf War.

The Overall Aim of the present proposal is to integrate, refine and investigate the feasibility (e.g., pilot testing, recruitment, attrition, assessment) of tDCS for treating chronic pain with a best practices evidence-based treatment for PTSD (i.e., Prolonged Exposure: PE) in 15 Gulf War veterans, a group for which both pain (fibromyalgia) and PTSD are particularly problematic.

SA1: Integrate the home-based tDCS+PE Treatment. The investigative team is comprised of Pain, PTSD, and salivary biomarker experts who will integrate tDCS into the 12 session PE treatment protocol.

H1: The 12 session PE protocol will yield itself well to tDCS component integration based on participant feedback.

SA2: Test the feasibility of both the integrated intervention and key study design features, including translational research features such as biomarker assessment in a non-randomized trial with 15 Gulf War Veterans assessed at baseline and post-treatment. Feasibility of the home-based tDCS+PE intervention will be measured in terms of recruitment metrics, assessment burden, successful biomarker collection, specification of biomarker relationship to hypothesized mechanisms of change, treatment attrition, rates of missing data at each measurement time point, participant satisfaction, and ratings of treatment face validity. Post treatment key informant interviews will be conducted where suggestions for treatment enhancement and satisfaction will be systematically collected and analyzed.

H2 is given in terms of Specific Pre-Defined Milestones for Success, including: 75% of Veterans experiencing chronic pain (fibromyalgia) and PTSD who enroll will complete at least 8 sessions of the integrated treatment, and both completers and dropouts will offer actionable suggestions in exit interviews for improving the delivery of the intervention. SA2) Feasibility metrics will be acceptable for recruitment rate (two per month), treatment completion of 8 sessions (75%), assessment completion (90%), and good to excellent satisfaction (95%)

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Presence of chronic non-cancer pain and pain interference, defined as scoring 1 standard deviation above PROMIS normative data on both the 3-item PROMIS Pain Intensity 3a scal and the 8-item PROMIS Pain 8a Interference scale. Symptoms will be required to be of six-month duration or longer
  • Diagnosis of PTSD assigned on the basis of the Clinician Administered PTSD Scale.

Exclusion criteria

  • Having a household member who is already enrolled in the study
  • Active psychosis or dementia at screening
  • Suicidal ideation with clear intent
  • Current substance dependence
  • current opioid medication for pain.

Treatment and study plan

Home-based tDCS

Device

tDCS is a non-invasive neuromodulation technique that has been used to improved cognitive functions. It will be administered with a constant current intensity of 2 mA57 for 20 min per session/ 10 sessions total daily for 2 weeks (Monday to Friday). The device is a Soterix 1x1 tDCS mini-CT Stimulator (Soterix Medical Inc., NY) with headgear and 5 _ 7 cm saline-soaked surface sponge electrodes.

Other names: Soterix 1x1 tDCS mini-CT Stimulator

Prolonged Exposure Therapy

Behavioral

Prolonged Exposure Therapy is a treatment for PTSD that includes the following components: a) psycho-education about the common reactions to traumatic events and presentation of the treatment rationale (sessions 1 and 2), b) repeated in vivo exposure to traumatic stimuli (in vivo exercises are assigned as homework during sessions 3 through 11), c) repeated, prolonged, imaginal exposure to traumatic memories (imaginal exposure is implemented during sessions 3 through 11; patients listen to session audiotapes for homework between sessions), and d) relapse prevention strategies and further treatment planning (session 12).

Primary outcomes

  1. Feasibility of Recruitment as Assessed by Number of Participants Enrolled in the Study

    Time frame: Week 0

  2. Feasibility of Biomarker Collection as Assessed by Number of Planned Saliva Samples Divided by Number of Planned Saliva Samples Collected

    Time frame: Week 12

  3. Feasibility of Biomarker Viability as Assessed by Percent of Viable Saliva Samples

    Time frame: Week 12

  4. Feasibility of Retention as Assessed by Number of Participants Who Complete at Least 8 Sessions

    Time frame: Week 12

  5. Feasibility of Data Collection as Assessed by Percent of Missing Data

    Time frame: Week 12

  6. Feasibility as Indicated by Satisfaction as Assessed by the Charleston Psychiatric Outpatient Satisfaction Scale

    Time frame: Week 12

    The Charleston Psychiatric Outpatient Satisfaction Scale total score ranges from 13 to 65, with a higher score indicating higher satisfaction.

  7. Feasibility as Indicated by Treatment Credibility as Assessed by a Credibility Scale

    Time frame: Week 12

    Treatment credibility will be assessed by a scale, with a total score ranging from 0 to 10, with 0 being "not credible, I did not think this treatment would help either my PTSD or Pain symptoms" to 10 being "completely credible, I was very sure this treatment would help both my PTSD and Pain symptoms."

  8. Feasibility as Indicated by Treatment Acceptability as Assessed by an Acceptability Scale

    Time frame: Week 12

    Treatment acceptability will be assessed by a scale, with a total score ranging from 0 to 10, with 0 being "not acceptable, this treatment should not be offered to veterans, those in pain, or those with PTSD" to 10 being "completely acceptable, this treatment is perfectly suited to veterans and others with pain and PTSD symptoms."

  9. Pain Interference as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 8a Interference Scale

    Time frame: Week 0

    PROMIS Pain interference 8a assesses self-reported consequences of pain on relevant aspects of one's life in the past 7 days. The measure includes 8-items rating pain from "Not at all" = 1 to "Very much" = 5, therefore the response range is 8-40 with higher scores indicating greater pain interference.

  10. Pain Interference as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 8a Interference Scale

    Time frame: Week 6

    PROMIS Pain interference 8a assesses self-reported consequences of pain on relevant aspects of one's life in the past 7 days. The measure includes 8-items rating pain from "Not at all" = 1 to "Very much" = 5, therefore the response range is 8-40 with higher scores indicating greater pain interference.

  11. Pain Interference as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 8a Interference Scale

    Time frame: Week 12

    PROMIS Pain interference 8a assesses self-reported consequences of pain on relevant aspects of one's life in the past 7 days. The measure includes 8-items rating pain from "Not at all" = 1 to "Very much" = 5, therefore the response range is 8-40 with higher scores indicating greater pain interference.

  12. Pain Intensity as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 3a Intensity Scale

    Time frame: Week 0

    PROMIS Pain intensity 3a is a self-report measure that assesses how much a person hurts (intensity or severity) in the past 7 days. The measure includes three items rating pain from "Had no pain" = 1 to "Very severe" = 5, therefore the response range is 3-15 with higher scores indicating greater pain intensity. Raw scores are reported.

  13. Pain Intensity as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 3a Intensity Scale

    Time frame: Week 6

    PROMIS Pain intensity 3a is a self-report measure that assesses how much a person hurts (intensity or severity) in the past 7 days. The measure includes three items rating pain from "Had no pain" = 1 to "Very severe" = 5, therefore the response range is 3-15 with higher scores indicating greater pain intensity. Raw scores are reported.

  14. Pain Intensity as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Pain 3a Intensity Scale

    Time frame: Week 12

    PROMIS Pain intensity 3a is a self-report measure that assesses how much a person hurts (intensity or severity) in the past 7 days. The measure includes three items rating pain from "Had no pain" = 1 to "Very severe" = 5, therefore the response range is 3-15 with higher scores indicating greater pain intensity. Raw scores are reported.

  15. PTSD Intensity as Assessed by the Clinician-Administered PTSD Scale 5 (CAPS-5)

    Time frame: Week 0

    Total possible scores on the CAPS-5 scale range from 0 to 80, with a higher score indicating greater PTSD intensity.

  16. PTSD Intensity as Assessed by the Clinician-Administered PTSD Scale 5 (CAPS-5)

    Time frame: Week 6

    Total possible scores on the CAPS-5 scale range from 0 to 80, with a higher score indicating greater PTSD intensity.

  17. PTSD Intensity as Assessed by the Clinician-Administered PTSD Scale 5 (CAPS-5)

    Time frame: Week 12

    Total possible scores on the CAPS-5 scale range from 0 to 80, with a higher score indicating greater PTSD intensity.

Secondary outcomes

  1. PTSD as Assessed by the PTSD Checklist-5 (PCL-5)

    Time frame: Week 0

    PCL-5 score ranges from 0 to 80, with a higher score indicating greater PTSD.

  2. PTSD as Assessed by the PTSD Checklist-5 (PCL-5)

    Time frame: Week 6

    PCL-5 score ranges from 0 to 80, with a higher score indicating greater PTSD.

  3. PTSD as Assessed by the PTSD Checklist-5 (PCL-5)

    Time frame: Week 12

    PCL-5 score ranges from 0 to 80, with a higher score indicating greater PTSD.

  4. Depression as Assessed by the Patient Health Questionnaire-9 (PHQ-9)

    Time frame: Week 0

    The PHQ-9 score ranges from 0 to 27, with a higher score indicating greater depression.

  5. Depression as Assessed by the Patient Health Questionnaire-9 (PHQ-9)

    Time frame: Week 6

    The PHQ-9 score ranges from 0 to 27, with a higher score indicating greater depression.

  6. Depression as Assessed by the Patient Health Questionnaire-9 (PHQ-9)

    Time frame: Week 12

    The PHQ-9 score ranges from 0 to 27, with a higher score indicating greater depression.

  7. Quality of Life as Assessed by the World Health Organization Quality of Life - Short Form (WHOQOL-BREF)

    Time frame: Week 0

    There are 4 domains on the WHOQOL-BREF, listed below, and for all domains a higher score indicates a greater quality of life.

    • physical health domain (7 items) - total score ranges from 7 to 35
    • psychological health domain (6 items) - total score ranges from 6 to 30
    • social relationships domain (3 items) 3 - total score ranges from 3 to 15
    • environmental health domain (8 items) - total score ranges 8 to 40

  8. Quality of Life as Assessed by the World Health Organization Quality of Life - Short Form (WHOQOL-BREF)

    Time frame: Week 6

    There are 4 domains on the WHOQOL-BREF, listed below, and for all domains a higher score indicates a greater quality of life.

    • physical health domain (7 items) - total score ranges from 7 to 35
    • psychological health domain (6 items) - total score ranges from 6 to 30
    • social relationships domain (3 items) 3 - total score ranges from 3 to 15
    • environmental health domain (8 items) - total score ranges 8 to 40

  9. Quality of Life as Assessed by the World Health Organization Quality of Life - Short Form (WHOQOL-BREF)

    Time frame: Week 12

    There are 4 domains on the WHOQOL-BREF, listed below, and for all domains a higher score indicates a greater quality of life.

    • physical health domain (7 items) - total score ranges from 7 to 35
    • psychological health domain (6 items) - total score ranges from 6 to 30
    • social relationships domain (3 items) 3 - total score ranges from 3 to 15
    • environmental health domain (8 items) - total score ranges 8 to 40

  10. Pain as Assessed by the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI)

    Time frame: Week 0

    There are 13 subscales of the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI), with each subscale ranging in score from 0 to 6, with a higher score indicating a greater degree of the domain assessed by the subscale.

  11. Pain as Assessed by the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI)

    Time frame: Week 6

    There are 13 subscales of the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI), with each subscale ranging in score from 0 to 6, with a higher score indicating a greater degree of the domain assessed by the subscale.

  12. Pain as Assessed by the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI)

    Time frame: Week 12

    There are 13 subscales of the West Haven-Yale Multidimensional Pain Inventory (WHYMPI/MPI), with each subscale ranging in score from 0 to 6, with a higher score indicating a greater degree of the domain assessed by the subscale.

  13. Kinesiophobia as Assessed by the Tampa Scale of Kinesiophobia-Revised (TSK-R)

    Time frame: Week 0

    Total score ranges from 17 - 68. A score of 17 is the lowest possible score, and indicates no kinesiophobia (that is, fear of pain with movement) or negligible kinesiophobia. A score of 68 is the highest possible score and indicates extreme kinesiophobia.

  14. Kinesiophobia as Assessed by the Tampa Scale of Kinesiophobia-Revised (TSK-R)

    Time frame: Week 6

    Total score ranges from 17 - 68. A score of 17 is the lowest possible score, and indicates no kinesiophobia (that is, fear of pain with movement) or negligible kinesiophobia. A score of 68 is the highest possible score and indicates extreme kinesiophobia.

  15. Kinesiophobia as Assessed by the Tampa Scale of Kinesiophobia-Revised (TSK-R)

    Time frame: Week 12

    Total score ranges from 17 - 68. A score of 17 is the lowest possible score, and indicates no kinesiophobia (that is, fear of pain with movement) or negligible kinesiophobia. A score of 68 is the highest possible score and indicates extreme kinesiophobia.

  16. Pain Catastrophizing as Assessed by the Pain Catastrophizing Scale (PCS)

    Time frame: Week 0

    Total scores ranges from 0 to 52, with a higher score indicating greater Pain Catastrophizing.

  17. Pain Catastrophizing as Assessed by the Pain Catastrophizing Scale (PCS)

    Time frame: Week 6

    Total scores ranges from 0 to 52, with a higher score indicating greater Pain Catastrophizing.

  18. Pain Catastrophizing as Assessed by the Pain Catastrophizing Scale (PCS)

    Time frame: Week 12

    Total scores ranges from 0 to 52, with a higher score indicating greater Pain Catastrophizing.

  19. Salivary Biomarker Measurement

    Time frame: Week 0

    Salivary levels of the biomarker panel (cortisol, substance P, DHEA, IL-1, and IL-6) using enzyme-linked immunosorbent assays (ELISA).

  20. Salivary Biomarker Measurement

    Time frame: Week 6

    Salivary levels of the biomarker panel (cortisol, substance P, DHEA, IL-1, and IL-6) using enzyme-linked immunosorbent assays (ELISA).

  21. Salivary Biomarker Measurement

    Time frame: Week 12

    Salivary levels of the biomarker panel (cortisol, substance P, DHEA, IL-1, and IL-6) using enzyme-linked immunosorbent assays (ELISA).

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jan 22, 2020
Registry last updated
Feb 3, 2023

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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