Mild Traumatic Brain Injury Clinical Trial
Official title:
Acupuncture Intervention in Subacute Mild Traumatic Brain Injury With Post-traumatic Stress Disorder: A Randomized Controlled Trial
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 |
Verified date | April 2022 |
Source | First Affiliated Hospital Xi'an Jiaotong University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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 |
Country | Name | City | State |
---|---|---|---|
China | First Affiliated Hospital of Xi'an Jiaotong University | Xi'an | Shaanxi |
Lead Sponsor | Collaborator |
---|---|
First Affiliated Hospital Xi'an Jiaotong University | Second Affiliated Hospital of Wenzhou Medical University |
China,
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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