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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02868671
Other study ID # NSFC81571752
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2016
Est. completion date September 2020

Study information

Verified date April 2022
Source First Affiliated Hospital Xi'an Jiaotong University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall goal of this study is to examine if acupuncture intervention can reduce the post-concussion symptom (PCS), and affective and cognitive complaints among mild traumatic brain injury (TBI). This study also hypothesized that compared to those in the sham acupuncture and waiting list control groups, patients in the real acupuncture group will have fewer symptoms of depression, sleep problems and post-concussion symptoms.


Description:

Project Background: Acupuncture has been shown in other settings to alleviate symptoms of TBI that are reported to be precursors of post-concussion symptom, including affective (depression, anxiety) and somatic (headache, sleep difficulties) complaints. Evidence suggests that the increased intensity of these symptoms, particularly greater affective distress and injury-associated pain, increases vulnerability to neurodegenerative disease and PTSD. By treating post-TBI symptoms with acupuncture, these predisposing conditions will improve, and, as a result, the incidence of PCS in this patient population will be reduced. Research plan: The overarching focus of this study is the use of acupuncture treatment, targeted to symptoms of mild TBI. The investigators propose a randomized, sham procedure and usual care-controlled clinical trial of acupuncture beginning at acute phase following mild traumatic brain injury (TBI). Participants meeting eligibility requirements will be randomized to 1 of 3 groups: verum acupuncture, sham acupuncture or waiting-list control. Acupuncture treatments will continue for one month, at which point all participants will be assessed for presence of mild TBI symptoms. Participants will be evaluated again after one-month acupuncture treatment and follow-up post-hospital discharge. The investigators hypothesize that true acupuncture will be more effective than sham acupuncture in reducing these outcomes at after treatment and follow-up stage. Patients were also scanned by 3T MRI scanner at baseline, one-month (after acupuncture treatment).


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date September 2020
Est. primary completion date August 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - subjects presenting to the study hospital emergency department (ED) after sustaining a acute head injury will be eligible if they: - are aged 18-75 years; - have a mild TBI, defined by the World Health Organization's Collaborating Centre for Neurotrauma Task Force (2005) - no contraindications to MR - injury within 7 days Exclusion Criteria: - experience with acupuncture treatment - history of neurological disease, long-standing psychiatric condition, spinal cord injury, head injury, or a history of substance or alcohol abuse - intubation and/or presence of a skull fracture - administration of sedatives on arrival in the emergency department, - the manifestation of mild traumatic brain injury (TBI) due to medications by other injuries (e.g., systemic injuries, facial injuries, or intubation) or other problems (e.g., psychological trauma, language barrier, or coexisting medical conditions), or caused by penetrating craniocerebral injury

Study Design


Intervention

Other:
acupuncture

sham acupuncture


Locations

Country Name City State
China First Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi

Sponsors (2)

Lead Sponsor Collaborator
First Affiliated Hospital Xi'an Jiaotong University Second Affiliated Hospital of Wenzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in PCS in patients following acupuncture treatments between baseline and after therapy Baseline, after one-month therapy
Secondary Changes in PCS in patients following acupuncture treatments between baseline and 6-12 months follow-up Baseline, 6-12 months follow-up
Secondary Diffusion tensor magnetic metrics changes in patients following acupuncture treatment baseline, one month
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