Exploratory Study to Evaluate 2 Acupuncture Methods for the Treatment of Headaches Associated With TBI

Last updated: May 11, 2016
Sponsor: Samueli Institute for Information Biology
Overall Status: Completed

Phase

2/3

Condition

Neurologic Disorders

Pain

Chronic Pain

Treatment

N/A

Clinical Study ID

NCT01338701
350890
  • Ages 18-69
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

This study investigates whether acupuncture can help to decrease the number and severity of headaches in people who have Traumatic Brain Injury. The aim of this study is to compare two different types of acupuncture—either Traditional Chinese Acupuncture or ear acupuncture—to a group that receives no acupuncture at all. Acupuncture has been demonstrated to reduce pain, improve health-related quality of life, prevent migraine headaches, and improve tension and chronic daily headaches.

Eligibility Criteria

Inclusion

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 daysprior

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

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

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

  3. Able to provide informed consent

Exclusion

Exclusion Criteria:

  1. Acupuncture treatment for any reason within the past month

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

  3. Unwillingness on the part of the participant to complete all study visits and/orcomponents 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 towarrant inpatient treatment in the medical or intensive care units

  7. Inability to give informed consent or complete study measures

Study Design

Total Participants: 45
Study Start date:
February 01, 2011
Estimated Completion Date:
April 30, 2015

Study Description

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

Connect with a study center

  • Walter Reed Army Medical Center

    Washington, D.C., District of Columbia 20307
    United States

    Site Not Available

  • Fort Belvoir Community Hospital

    Alexandria, Virginia 22060
    United States

    Site Not Available

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