Brain Biomarkers w/Mind-Body Tx in Veterans With Post Traumatic Headache (PTH)

Post Traumatic Headache Clinical Trial

— MBSR-PTH  

Official title:

Neuroimaging Biomarkers of Mind-Body Treatment in Veterans With Post Traumatic Headache (PTH)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02145117
• Other study ID #: 13-000864
• Secondary ID: R01AT007137
• Status: Active, not recruiting
• Phase: N/A
• First received: May 20, 2014
• Last updated: December 5, 2017
• Start date: September 2013
• Est. completion date: September 27, 2018

Study information

• Verified date: December 2017
• Source: University of California, Los Angeles
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This project aims to develop and test structural and functional brain imaging biomarkers for improvement in chronic pain from a mind/body intervention perspective in a critical veteran population, namely veterans with post traumatic headache (PTH) associated with mild traumatic brain injury (TBI). The project also aims to examine feasibility in a sample of veterans with PTH of performing resting state and structural neuroimaging protocols, and of obtaining active participation and completion of MBSR training. Lastly, exploratory analysis of brain imaging data will be performed to determine if hypothesized candidate biomarkers are associated with positive outcomes from MBSR and determine estimated effect sizes for future studies in PTH population.

Description:

Returning veterans from Iraq and Afghanistan (OIF/OEF veterans) have a very high incidence of TBI (14-23%) with the largest number having mild TBI (i.e., no discernible structural brain damage) with 63.5% having persistent headache. Treatment of PTH in this population has been difficult and mind/body interventions including Mindfulness Based Stress Reduction (MBSR) may offer significant benefit. A biomarker that will support clinical endpoints ("surrogate endpoint") and help predict clinical benefit, could be used to more efficiently and completely assess mind/body treatment effects in clinical trials for PTH, compare various complementary and alternative medicine (CAM) treatments, and potentially target specific treatments to patients most likely to benefit. This project aims to investigate candidate biomarkers for MBSR response in veterans with PTH. Primarily, all subjects if they are interested and appropriate for the study, will undergo a screening at their regular clinic visit at the VAGLAS physical medicine and rehab department. If a subject responds to advertisement they will be screened using the same tools and enrollment criteria required for the veterans at VAGLAS. We expect we will need to enroll and screen no less than 33 subjects in order to complete 20 evaluable subjects for analysis. The study subjects will be evaluated for the severity of their PTH, the impact of PTH on their life, and the extent of the disease/pain condition. If eligible the nurse coordinator will contact them to schedule the pre-MBSR functional MRI visit. At the MRI we will evaluate patterns of activity (functional connectivity) in the brain at rest, and look at cortical thickness. Following the MRI visit all subjects will complete a 9-week modified MBSR training with a qualified instructor. Mid-study (after MBSR class 4) the subject will be asked to complete mid-study questionnaires at home on Survey Monkey or on paper if they choose. At the end of the MBSR training in which the subject will have to complete at least 3 visits, functional (f)MRI procedure will be repeated and compared against the first. Three months after completing the study there will be a follow-up visit to complete behavioral/symptom/quality of life questionnaires on line via SurveyMonkey. This is to see if the changes in the biomarkers will mediate changes in these behavioral measures 3-mo post Treatment (i.e. measure stability).

All in all, to complete the study subjects will have a screening visit, pre and post training MRI visit, up to 9 MBSR training visits, mid study questionnaires, a 4-hr retreat visit after week 6 and a final 3-mo f/u visit for questionnaires only.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 20
• Est. completion date: September 27, 2018
• Est. primary completion date: September 27, 2018
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Males and female veterans at least 18 years of age

• Mild post traumatic headaches, diagnosed by a physician

• No prior training in MBSR or other mindfulness or meditation training will be allowed

• Able to read and speak English

• No participation in a clinical trial within the last 28 days

Exclusion Criteria:

• Current severe psychiatric diagnoses (e.g., schizophrenia, bipolar disorder, claustrophobia, history of panic attacks)

• Significant co-morbid condition(s) such as insulin-dependent diabetes, cancer, obesity (BMI>35), severe lung disease, neurological conditions (e.g., seizures), uncontrolled hypertension, or significant heart disease

• History of persistent headaches prior to TBI

• Unsafe for MRI (e.g., metal objects/shrapnel, metallic implants, brain or skull abnormalities, and claustrophobia)

• Use of centrally acting medications that will interfere with the neuroimaging testing (e.g. narcotic medications)

• Daily use of illicit drugs or marijuana

• Daily alcohol consumption of greater than 2 units

Related Conditions & MeSH terms

• Headache
• Post Traumatic Headache
• Post-Traumatic Headache

Intervention

Behavioral:
• MBSR
Behavioral

Locations

Country	Name	City	State
United States	VA West Los Angeles Medical Center	Los Angeles	California

Sponsors (3)

Lead Sponsor	Collaborator
University of California, Los Angeles	National Center for Complementary and Integrative Health (NCCIH), VA Medical Center-West Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Validate Optimal Biomarker candidates	To validate optimal brain biomarker candidates by assessment of treatment responsiveness in post traumatic headache following a 9 week course in Mindfulness Based Stress Reduction (MBSR)	After MBSR training (9 weeks)
Secondary	Specificity, generality and moderation of biomarker response to MBSR treatment	Specificity of biomarker response to MBSR measured by changes in selected biomarker candidates correlation with improvement in mindfulness at end of treatment and 3-month follow-up.; Determine generality of optimal biomarkers via examination of factors such as sex, age, co-morbid pain, mood, and/or baseline severity, as moderators of biomarker performance.	Post MBSR training at 3 month follow up