Concussion Post Syndrome

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

Condition / disease
Location
Status: Not yet recruiting

Post-Concussion Sleep and Brain-heart Functions

This project is designed as a randomized controlled trial (RCT), with an active control group. Sleep and heart rate will be monitored at home for 1 week before and after the intervention. Questionnaires will be completed from home before, during and 8 weeks after the end of the Intervention. The Cognitive Behavioural Therapy for Insomnia, adapted for post-concussed individuals (CBT-pI) and control interventions, will be delivered on a digital online platform over an 8-week period. Participants in the control arm will be offered CBT-pI after the follow-up period. All intervention arms will be delivered as adjuncts to standard clinical care. All other treatments received during the intervention will be documented.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of OttawaUpdated: Jun 11, 2026
Eligibility criteria

Adults 18 years and older [+4]

Having undergone another CBT-I program within the past 6 months [+9]

Status: Not yet recruiting

Intravenous Metoclopramide Versus Intravenous Acetaminophen for Acute Concussion Treatment

The IMPACT study is a randomized, double-blind clinical trial evaluating two commonly used intravenous medications - metoclopramide and acetaminophen - for treating acute post-concussion symptoms in emergency department patients after mild head injury. The study aims to determine which treatment more effectively improves symptoms such as headache, dizziness, nausea, concentration difficulties, and emotional changes within the first week after injury. Participants will be enrolled across two Montefiore emergency departments and followed using a validated post-concussion symptom questionnaire. Findings from this study may help improve evidence-based treatment strategies for patients experiencing concussion-related symptoms after head trauma.

Participants needed: 200
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Montefiore Medical CenterUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Adults presenting to one of the study emergency departments (EDs) [+6]

Already treated with an anti-dopaminergic medication for post-concussion symptom... [+6]

Status: Not yet recruiting

Female Concussion Head Cooling

This research is being done to examine the benefits of a 28 day head cooling intervention on cognition, inflammation of the brain, sleep quality, menstrual symptom interaction, and mood in acutely concussed females. Brain cooling has been shown to cause temporary symptom relief after traumatic brain injury, but its implications for decreasing timeline of full concussion recovery, particularly in females during periods of confounding neuropsychological menstrual symptoms, remains unexplored.

Participants needed: 32
Trial details
Age: 18-27Biological sex: FemaleType: InterventionalSponsor: Penn State UniversityUpdated: Dec 26, 2025Locations: 1
Eligibility criteria

Require that any participant is 18-27 years old [+3]

Exclude persons under 18 years old or over 27 years old [+8]

Status: Recruiting

Auditory Slow Wave Enhancement After Concussion

The prevalence of a traumatic brain injury (TBI) in children and adolescents is around 30% with 70-90% being classified as mild (concussion). Because the brain of a child is still developing, a TBI can have devastating effects and possibly creates lifetime challenges. Sleep seems to play an important role in the post-concussion recovery process. Auditory stimulation during sleep has been shown to reliably boost slow waves, a solid marker for the depth of sleep, and can thus be used to deepen sleep. This study aims to investigate the effects of sleep enhancement via auditory stimulation on recovery after a concussion in children and adolescents in their home. Therefore, half of the patients receive one week of auditory stimulation during deep sleep at their home using a mobile device. The other half follows the same study protocol, but no tones are administered (sham). Cognitive tests as well as symptom questionnaires are used to assess the recovery process. It is hypothesized that the patients in the intervention group will recover better than the ones who haven't received the intervention. Additionally, a group of children and adolescents who never sustained a concussion is included as a control.

Participants needed: 120
Trial details
Age: 6-18Biological sex: AllType: InterventionalSponsor: University Children's Hospital, ZurichUpdated: Dec 9, 2024Locations: 1
Eligibility criteria

Informed Consent as documented by signature [+3]

Preterm birth (< 37 gestational weeks) [+12]