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The Effects of Acupuncture on the Risk of AD After TBI

Primary Purpose

Brain Injuries, Traumatic

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Acupuncture
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Injuries, Traumatic focused on measuring Brain Injuries, Traumatic, Alzheimer's disease, Magnetic resonance imaging, white matter integrity, beta-Amyloid

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. age ≥ 20 years old
  2. GCS score > 13
  3. LOC < 30 minutes
  4. hospital admission < 7 days
  5. having adequate competency for understanding the study and a willingness to sign the written informed consent forms
  6. be able to commence the acupuncture intervention within 2 weeks after TBI diagnosis

Exclusion Criteria:

  1. medical history of neurological, cardiovascular events, or mental disorder, e.g., epilepsy, stroke, major depression or anxiety
  2. other major medical conditions, e.g., active cancer, uncontrolled diabetes, pregnancy
  3. surgery for TBI
  4. receipt of acupuncture within the 6 months prior to study entry
  5. patients with pacemaker, metal graft, or claustrophobia
  6. preparing for pregnancy during the trial

Sites / Locations

  • China Medical University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Acupuncture group

Control group

Arm Description

Disposable acupuncture needles will be inserted into acupoints for a depth of 10-30 mm in a direction oblique or parallel to the surface. To ensure allocation concealment, all needles will be affixed with plastic O-rings and adhesive tapes.

Streitberger's non-invasive placebo acupuncture needles will be used in the control group; blunt-tipped needles will touch the skin quickly without being inserted. To ensure allocation concealment, all needles will be affixed with plastic O-rings and adhesive tapes.

Outcomes

Primary Outcome Measures

Decreased plasma levels of Aβ peptide
Decreased plasma levels of tau
Decreased plasma levels of glial fibrillary acidic protein (GFAP)

Secondary Outcome Measures

Increased white matter integrity

Full Information

First Posted
December 8, 2017
Last Updated
March 6, 2018
Sponsor
China Medical University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03378037
Brief Title
The Effects of Acupuncture on the Risk of AD After TBI
Official Title
The Effects of Acupuncture on the Risk of AD After TBI: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
December 25, 2017 (Actual)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
China Medical University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Traumatic brain injury (TBI) is a severely disabling injury which affects 150-200 people per million annually. Increasing evidence suggests that TBI may be a major risk of dementia, Alzheimer's disease (AD) in particular. Postmortem evidence has shown that beta-amyloid (Aβ) deposits, one of the most validated pathological biomarkers of AD, are present in the brains of severe TBI patients. Although the underlying mechanisms remain unclear, the axonal injury may play a role. Imaging investigations have revealed Aβ density maps of TBI patients overlapped with those of AD patients, and increased Aβdensity not only associated with prolonged TBI duration but also associated with decreased white matter integrity. Hence, the increasing accumulation in Aβ due to TBI may contribute to the initiation of the pathological alterations seen in AD. Treatment of TBI may not only be of benefit for the injury itself but also act to block the pathological changes in AD. As a part of the clinical arm of the project, in this subproject investigators will conduct a single-blind, block-randomized clinical trial to investigate the efficacy of acupuncture in TBI. More specifically, investigators hypothesize that acupuncture intervention will elicit neuroprotective processes and thereby reduce axonal damage in TBI, manifested as (1) decreased plasma levels of Aβ peptide, tau, and glial fibrillary acidic protein (GFAP) and (2) increased white matter integrity after acupuncture. Ninety-six participants will be randomly allocated to the acupuncture intervention (verum acupuncture) or control group (sham acupuncture) in a 1:1 ratio. All participants will receive 20 minutes of acupuncture treatment twice a week for 2 weeks. A set of commonly used acupoints for TBI treatment will be manually stimulated every 10 minutes. The multi-modality magnetic resonance imaging (T1, T2, and diffusion tensor imaging) and blood sample will be taken before and after the acupuncture session to measure the white matter integrity in brain and plasma levels of Aβ peptide, tau, and GFAP, respectively. After integrate these data with other subprojects, we can provide synergic and integrative mechanisms of the effects of acupuncture on the risk of AD after TBI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Traumatic
Keywords
Brain Injuries, Traumatic, Alzheimer's disease, Magnetic resonance imaging, white matter integrity, beta-Amyloid

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
76 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Acupuncture group
Arm Type
Experimental
Arm Description
Disposable acupuncture needles will be inserted into acupoints for a depth of 10-30 mm in a direction oblique or parallel to the surface. To ensure allocation concealment, all needles will be affixed with plastic O-rings and adhesive tapes.
Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
Streitberger's non-invasive placebo acupuncture needles will be used in the control group; blunt-tipped needles will touch the skin quickly without being inserted. To ensure allocation concealment, all needles will be affixed with plastic O-rings and adhesive tapes.
Intervention Type
Procedure
Intervention Name(s)
Acupuncture
Intervention Description
20 minutes of acupuncture treatment, twice a week for 2 weeks. Acupoints will be manually stimulated every 10 minutes.
Primary Outcome Measure Information:
Title
Decreased plasma levels of Aβ peptide
Time Frame
After 2-week acupuncture treatment interval
Title
Decreased plasma levels of tau
Time Frame
After 2-week acupuncture treatment interval
Title
Decreased plasma levels of glial fibrillary acidic protein (GFAP)
Time Frame
After 2-week acupuncture treatment interval
Secondary Outcome Measure Information:
Title
Increased white matter integrity
Time Frame
After 2-week acupuncture treatment interval

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age ≥ 20 years old GCS score > 13 LOC < 30 minutes hospital admission < 7 days having adequate competency for understanding the study and a willingness to sign the written informed consent forms be able to commence the acupuncture intervention within 2 weeks after TBI diagnosis Exclusion Criteria: medical history of neurological, cardiovascular events, or mental disorder, e.g., epilepsy, stroke, major depression or anxiety other major medical conditions, e.g., active cancer, uncontrolled diabetes, pregnancy surgery for TBI receipt of acupuncture within the 6 months prior to study entry patients with pacemaker, metal graft, or claustrophobia preparing for pregnancy during the trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yu-Chen Lee, Doctor
Phone
886-975-682023
Email
d5167@mail.cmuh.org.tw
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
ZIP/Postal Code
404
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yu-Chen Lee, Doctor
Phone
0975-682023
Email
d5167@mail.cmuh.org.tw

12. IPD Sharing Statement

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The Effects of Acupuncture on the Risk of AD After TBI

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