The Effects of Acupuncture on the Risk of AD After TBI
Brain Injuries, Traumatic
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
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
Sites / Locations
- China Medical University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Acupuncture group
Control group
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.