An Exploratory Study to Evaluate Two Acupuncture Methods for the Treatment of Headaches Associated With Traumatic Brain Injury

This is a 12 week study. If eligible, participants will be randomly assigned to 1of 3
groups: ear acupuncture, Traditional Chinese Acupuncture, or the usual care group.

Subjects receiving acupuncture will:

- meet with one of the acupuncturists who will conduct her first assessment

- come to Walter Reed Army Medical Center (WRAMC) 10 times over a 6-week period to
receive acupuncture treatments from a licensed acupuncturist

Subjects in the usual care group will:

- not receive any acupuncture treatments

- continue usual treatment plan

- be given the option to receive 10 acupuncture treatments between the 6- and 12-week
period

All subjects will also:

- complete questionnaires at 3 different times: baseline (beginning of study), after 6
weeks, and after 12 weeks. These questionnaires will assess headaches, overall health
and quality of life

- complete a daily headache diary

- continue to be treated for their headaches

- continue taking prescription and over-the-counter medications for any conditions being
treated

Inclusion Criteria:

1. 18-69 years of age

2. Service Members with previous deployment to war zone

3. Non-acute mild to moderate traumatic brain injury as defined by:

- Injury event (i.e., blast, fall, MVC, head impact) that occurred at least 7 days
prior

- Loss of consciousness (if present) for less than 24 hours and alteration of
consciousness or posttraumatic amnesia for less than one week

4. Presence of headache or any etiology requiring self-medication or medical management
with at least 4 headache days in the past 4 weeks

5. Rancho Los Amigos Cognitive Scale score of greater than or equal to 7

6. Able to provide informed consent

Exclusion Criteria:

1. Acupuncture treatment for any reason within the past month

2. Any active unstable psychiatric condition, including active psychosis, suicidal or
homicidal ideation

3. Unwillingness on the part of the participant to complete all study visits and/or
components of the intervention

4. Scheduled surgery during the treatment phase of the study

5. Pregnancy or breastfeeding at time of study enrollment or during study participation

6. Any medically unstable condition that in the opinion of the P.I. has the potential to
warrant inpatient treatment in the medical or intensive care units

7. Inability to give informed consent or complete study measures