Concussion

6

Review clinical trials related to Concussion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Rehabilitation, Education, and SElf-management for Adolescents After Mild Traumatic Brain Injury

Concussion or mild traumatic brain injury (mTBI) is a major public health concern. Most adolescents will recover from mTBI without complication; however, a sizeable minority experience symptoms that last more than one most post-injury (i.e., persisting symptoms after concussion). Few evidence-based treatments exist for adolescents with persisting symptoms after concussion. Mindfulness-based interventions (MBIs) are effective for treating a wide range of mental and physical health conditions that overlap with post-concussion symptoms. Participants will participate in an 8-week smartphone app-based MBI or a health education program as a control. The study will determine the practicality of doing a larger study to evaluate the effectiveness of the MBI by assessing participants' level of interest, view of intervention helpfulness, and their completion of all the components of the study.

Participants needed: 72
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Molly CairncrossUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Age 12-18 [+4]

Parent- or self-reported psychiatric hospitalization in past year or prior diagn... [+1]

Status: Not yet recruiting

BCAAs in Concussion 3.0

This study is a randomized, placebo-controlled, double-blinded, therapeutic exploratory clinical trial of branched chain amino acids (BCAAs) in the treatment of concussion. The aim of the study is to determine whether administration of high-dose BCAAs compared to placebo promotes concussion recovery.

Participants needed: 150
Trial details
Phase: Phase 2Age: 11-23Biological sex: AllType: InterventionalSponsor: Akiva CohenUpdated: Jun 26, 2026
Eligibility criteria

Males and females,11 - 23 years of age. [+5]

Evidence of moderate or severe TBI, including GCS <13, TBI requiring hospital ad... [+5]

Status: Recruiting

rTMS for Military TBI-related Depression

The purpose of this study is to investigate the efficacy, safety, and tolerability of two dorsolateral prefrontal cortex (DLPFC) repetitive transcranial magnetic stimulation (rTMS) protocols to alleviate symptoms of depression in United States (U.S.) military service members and veterans with a history of concussion/mild traumatic brain injury (TBI).

Participants needed: 198
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Henry M. Jackson Foundation for the Advancement of Military MedicineUpdated: Apr 29, 2026Locations: 3
Eligibility criteria

Age 18-55 at the time of consent. Older individuals will not be enrolled in this... [+10]

History of unprovoked seizures. [+22]

Status: Not yet recruiting

Optimized, Neuroplasticity-Enhanced-Depression (ONE-D) Transcranial Magnetic Stimulation (TMS) Treatment for Female Athletes With Co-morbid Depression and Concussion

Concussion and depression have long been recognized to be intertwined pathologies.1-3 Although female athletes are more likely to suffer from mental health symptoms than males athletes following a concussion,2 research in this area has been largely biased toward males.4 Recently functional MRI (fMRI) studies5 in concussed athletes have established that there are patterns of local alterations in neural connectivity in the frontal cortex that demonstrate anatomic congruency with transcranial magnetic stimulation (TMS) studies that mapped alternations in neural connectivity to functional and somatic symptoms.6 Thus, there is potential that TMS treatment could decrease both symptom profiles, revolutionizing comorbid treatment options. Possible Benefits: Previous studies have showed a 70% remission rate for depression symptoms. It is possible that participants could have improvement in depressive or concussive symptoms after the ONE-D TMS treatment.

Participants needed: 35
Trial details
Phase: Phase 2, Phase 3Age: 18-65Biological sex: FemaleType: InterventionalSponsor: University of FloridaUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Female athletes, both recreational and professional [+4]

Pregnant or breast-feeding individuals [+10]

Status: Recruiting

Retinal Imaging in Neurodegenerative Disease

This study aims to develop and evaluate biomarkers using non-invasive optical coherence tomography (OCT) and OCT angiography (OCTA) as well as ultra-widefield (UWF) fundus photography to assess the structure and function of the retinal and choroidal microvasculature and structure in persons with mild cognitive impairment (MCI) and Alzheimer's Disease (AD), Parkinson's Disease (PD), or other neurodegenerative disease, diseases as outlined.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Duke UniversityUpdated: Feb 4, 2026Locations: 1
Eligibility criteria

Adults with neurodegenerative disease ((MCI, PD, AD, FTD, DLB, ALS, MS, HD, TBI,... [+1]

Inability to cooperate with or complete testing or other neurologic or age- rela... [+1]

Status: Not yet recruiting

Cervico-vestibular Home Exercise Program Feasibility

The purpose of this pilot study is to: 1. Determine the feasibility of adherence to completing the home cervico-vestibular exercise program following concussion. 2. Investigate the acceptability of the cervico-vestibular home exercise program. 3. Investigate the impact of the cervico-vestibular home exercise program on symptom reduction, return to play, and return to learn 4. Analyze the timing at which a home exercise program is typically prescribed. Participants will be asked to do and keep track of exercises made to help in their concussion recovery over a two-week period. Participants will come back to see their doctor and complete surveys about how easy the exercises were to do and if they liked them.

Participants needed: 30
Trial details
Age: Up to 17Biological sex: AllType: InterventionalSponsor: Texas Scottish Rite Hospital for ChildrenUpdated: Aug 1, 2025Locations: 1
Eligibility criteria

Patients <18 years old [+6]

Patients ≥18 years old [+5]