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

S

Samueli Institute for Information Biology

Status and phase

Completed
Phase 3
Phase 2

Conditions

Traumatic Brain Injury
Headache

Treatments

Procedure: Auricular (Ear) Acupuncture
Other: Usual Care
Procedure: Traditional Chinese Acupuncture (TCA)

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

Details and patient eligibility

About

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.

Full 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

Enrollment

45 patients

Sex

All

Ages

18 to 69 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Auricular (Ear) Acupuncture
Experimental group
Description:
Auricular (Ear) Acupuncture is administered in a step-wise, algorithmic acupuncture approach in which needles are inserted at specific auricular landmarks. The sequence and location of needled points is determined by the participant's severity of headache pain at presentation and response to needling. Between six and nine points are needled in each treatment session depending on the individual's response (i.e., a decrease or persistence of headache pain). In-dwelling ASP needles are inserted at the end of each session. Participants are instructed to remove the needles after 3 days, or sooner if pain or redness developed at a needle site. Ten 45-minute acupuncture treatment sessions are administered over 6 weeks.
Treatment:
Procedure: Auricular (Ear) Acupuncture
Traditional Chinese Acupuncture (TCA)
Experimental group
Description:
A semi-standardized form of Traditional Chinese Acupuncture (TCA) is administered, incorporating the insertion of up to 22 acupuncture needles associated with each individual participant's: (1) primary headache pattern (up to three pairs of points); (2) secondary headache pattern (up to 2 pairs of points); (3) Ah-Shi or tender points (up to 4 points); (4) constitutional points (source points on two meridians); and, (5) up to 2 pairs of additional points from a selected list. Point selection was reassessed every two weeks per TCM diagnostic and treatment principles. While the majority of points were located on the limbs, points also included local points of tenderness to the head, as well as the front and back of the torso. Ten 60-minute TCA sessions are administered over 6 weeks.
Treatment:
Procedure: Traditional Chinese Acupuncture (TCA)
Usual Care
Other group
Description:
All study participants continue to receive routine usual care for their TBI, headaches and associated symptoms as determined by their clinical team.
Treatment:
Other: Usual Care

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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