Cognitive Performance

16

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

Condition / disease
Location
Status: Not yet recruiting

Phosphatidylserine, Taurine, and Caffeine for Cognitive Fatigue in Professional Football Players

This randomized, double-blind, placebo-controlled, parallel-group trial will evaluate the effects of 14 days of taurine-caffeine supplementation with or without phosphatidylserine on neurocognitive fatigue resistance, visual search efficiency, and football-specific tactical decision-making in professional male football players. Sixty-two male outfield football players from two professional clubs will be randomized to placebo, taurine plus caffeine, or taurine plus caffeine plus phosphatidylserine. Laboratory and field-based outcomes will be assessed at baseline and after the supplementation period.

Participants needed: 62
Trial details
Age: 18-37Biological sex: MaleType: InterventionalSponsor: Vizja University in WarsawUpdated: Jul 13, 2026Locations: 2
Eligibility criteria

Male professional outfield football players aged 18 to 37 years. [+7]

Goalkeepers. [+10]

Status: Recruiting

Examining the Efficacy of Short-Term Intensive PTSD Treatment on Psychological and Cognitive Impairment Symptoms

Our long-term goal is to provide rapid and sustained reductions of trauma and cognitive-related symptoms among Special Operations personnel with PTSD or subthreshold PTSD. The primary objective of this project is to examine the effectiveness of massed PTSD treatment (i.e., CPT and EMDR) in "real-world" military settings. CPT and EMDR are both empirically supported psychotherapies for PTSD. To accomplish this objective, we will enroll military personnel meeting diagnostic criteria for PTSD or subthreshold PTSD (i.e., meeting threshold levels for 3 of 4 symptom criteria).

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ohio State UniversityUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

(1) substance use disorder requiring medical management; (2) imminent suicide ri...

Status: Recruiting

A Clinical Trial to Investigate the Safety and Efficacy of AP-Brain on Cognitive Performance at Varying Dosages in Healthy Middle-aged and Older Adults With Self-reported Memory Problems

The goal of this clinical trial is to investigate the safety and efficacy of AP-Brain on cognitive performance at varying dosages in healthy middle-aged and older adults with self-reported memory problems. The main question it aims to answer is: What is the effect of AP-Brain at 1 g, 3 g, and 5 g on cognitive performance? Participants will be asked to consume AP-Brain at 1 g, 3 g, or 5g, or Placebo and asked to complete memory assessment questionnaires.

Participants needed: 120
Trial details
Age: 40-79Biological sex: AllType: InterventionalSponsor: Rousselot BVBAUpdated: Jun 24, 2026Locations: 2
Eligibility criteria

Males and females 40-79 years of age, inclusive [+17]

Individuals who are pregnant, breast feeding, or planning to become pregnant dur... [+30]

Status: Not yet recruiting

Effects of Caffeine on Chess Performance and Cognitive Function in Professional Chess Players

This study will examine whether caffeine improves cognitive and competitive performance in professional chess players during tournament-style games. In a randomized double-blind crossover design, participants will complete two experimental sessions in which they consume either caffeinated coffee or decaffeinated coffee before playing a standardized chess match. Cognitive performance will be assessed using attention and reaction-time tests, including the Stroop Test, Trail Making Test, and Puzzle Rush task. Chess performance outcomes such as move accuracy, time management, and error rates will also be evaluated. The study aims to determine whether moderate caffeine intake enhances focus, alertness, and decision-making during prolonged competitive chess play.

Participants needed: 12
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Male and female professional chess players aged 18-50 years [+4]

Non-caffeine users [+11]

Status: Not yet recruiting

Cognitive Responses to Acute Breath-Hold Diving Training in Female Divers

This study aims to investigate the acute cognitive and physiological responses to breath-hold diving training in trained female divers. Participants will complete three separate sessions including a control session, a land-based breath-hold training session, and a water-based breath-hold training session in randomized order. Cognitive performance, mood state, heart rate responses, respiratory function, and maximal breath-hold capacity will be evaluated before and after the interventions. The study is expected to improve understanding of how acute apnea-based diving exercises influence cognitive functions and physiological adaptations under different environmental conditions.

Participants needed: 30
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Istanbul Gelisim UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Licensed breath-hold or free-diving athletes [+6]

Use of performance-enhancing drugs or ergogenic aids [+5]

Status: Recruiting

Post-stroke Cognitive Impairment

Present study aims to track the post-stroke cognitive trajectories and to investigate its inter-individual variability.

Participants needed: 600
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Roza UmarovaUpdated: May 6, 2026Locations: 1
Eligibility criteria

Age ≥18 years old [+2]

Previous stroke anamnestic or based on clinical imaging [+5]

Status: Not yet recruiting

EEG-Guided Binaural Beat Audio to Reduce Performance-Related Stress and Improve Cognition

Performance-related stress can impair sustained attention, inhibitory control, and memory. This randomized, double-blinded, sham-controlled parallel-arm trial evaluates whether a 30-minute EEG-guided binaural beat audio intervention reduces subjective stress/performance anxiety and improves cognition, and whether it changes task-related brain reactivity measured by fMRI. The intervention uses real-time single-electrode EEG recorded over the left prefrontal cortex to dynamically adjust binaural beat frequencies to guide the brain toward a target state; the sham condition uses non-binaural music delivered through identical headphones. Adult music majors preparing for an upcoming concert will complete pre- and post-intervention fMRI sessions during cognitive/music tasks (Stop Signal Reaction Task, Music Reading Task, Music Memory Retrieval Task) and complete visual analog scales (VAS) assessing performance anxiety, stress, and related subjective states. The primary outcomes include fMRI task-related activity in stress-regulation regions (dlPFC, amygdala, hippocampus), behavioral inhibition indices from the stop-signal task, music memory retrieval accuracy, and VAS-reported stress/performance anxiety.

Participants needed: 32
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Texas Tech University Health Sciences CenterUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Adults (18+ years) enrolled as undergraduate music majors at Texas Tech Universi... [+2]

Subjects with contraindications to undergo MRI after being screened by the TTNI... [+10]

Status: Recruiting

L-serine and Strength Training in the Elderly

This study investigates whether taking the amino acid L-serine, either alone or in combination with targeted strength training, can have a positive effect on mental performance, brain function, and physical fitness in older people. Healthy, independent women and men aged 65 to 85 are eligible to participate. Participants will be randomly assigned to one of three groups: placebo, L-serine, or L-serine combined with strength training. Cognitive tests, physical performance tests, and blood and brain tests will be conducted over a period of 48 weeks. The aim is to gain a better understanding of how nutrition and exercise can contribute to healthy aging.

Participants needed: 126
Trial details
Age: 65-85Biological sex: AllType: InterventionalSponsor: University of ViennaUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Men and women between the ages of 65 and 85 [+2]

Chronic diseases that contraindicate medical training therapy [+6]

Status: Not yet recruiting

Long-Term Effects of Walnut Consumption on Brain Function

Rationale: Healthy foods, including mixed nuts, may improve brain function, which is essential for cognitive and metabolic health, and may contribute to improved food intake regulation. It is therefore important to investigate the specific effects of walnuts on cerebral blood flow responses before and after intranasal insulin administration, as well as their associated functional benefits. The investigators hypothesize that long-term walnut consumption improves vascular function and insulin-sensitivity in the brain, thereby enhancing cognitive performance and appetite control in abdominally obese men and women. Objective: The primary objectives are to investigate in abdominally obese adults the effects of 24-week walnut consumption on (regional) vascular function and insulin-sensitivity in the brain, while the investigators will also assess changes in cognitive performance and appetite-related brain reward activity (secondary objectives). Cerebral blood flow responses before (brain vascular function) and after the administration of intranasal insulin spray (brain insulin-sensitivity) will be quantified by the non-invasive gold standard magnetic resonance imaging (MRI)-perfusion method Arterial Spin Labeling (ASL). Study design: This intervention study will have a randomized, controlled parallel design. The total study duration will be 24 weeks. Study population: Fifty-five abdominally obese men and (postmenopausal) women (aged 45-75 years) without a history of cardiovascular diseases or complaints will participate. This study population is expected to have a decreased cerebral blood flow at baseline and are also at increased risk of cognitive impairment, allowing for improvement by the intervention. Intervention: Study participants will receive daily 50 g (about 15% of energy) of raw walnuts (walnut intervention) or no walnuts (control intervention) for 24 weeks. Main study parameters/endpoints: At baseline and after 24 weeks (follow-up), participants will visit the research facilities for assessments. The primary endpoint is the difference in the cerebral blood flow response before and after intranasal insulin administration between the walnut and control intervention. Cognitive performance will be assessed, while the investigators will also focus on appetite-related brain reward activity (secondary outcomes).

Participants needed: 55
Trial details
Age: 45-75Biological sex: AllType: InterventionalSponsor: Maastricht University Medical CenterUpdated: Feb 19, 2026Locations: 1
Eligibility criteria

Men and women, aged between 45-75 years [+9]

Allergy or intolerance to walnuts [+12]

Status: Not yet recruiting

High-Dairy Food Patterns and Gut-Brain Axis

Disturbances in brain insulin sensitivity are associated not only with obesity and type 2 diabetes, but also with brain aging and cognitive decline. Longitudinal studies suggest that dietary patterns, particularly those high in dairy intake, may impact brain function via the gut-brain axis. Indeed, dairy foods are known to modulate gut microbiota and may, through this pathway, not only improve brain insulin sensitivity and cognitive performance, but also mental health and appetite regulation. However, underlying mechanisms remain largely unexplored. The primary objective of this study is to evaluate, in older adults with overweight or obesity, the effects of a high-dairy food pattern (4-5 daily servings of (butter)milk, cheese, yogurt, or cottage cheese) compared to a low-dairy food pattern (≤1 serving daily) on (regional) brain vascular function and insulin sensitivity. These outcomes will be quantified using the non-invasive MRI perfusion technique Arterial Spin Labeling (ASL), which assesses cerebral blood flow (CBF) in response to intranasal insulin, a validated physiological marker of brain insulin sensitivity. Secondary objectives include changes in cognitive performance (via the CANTAB neuropsychological test battery), gut microbiota composition (via shotgun metagenomic analysis of fecal samples), and appetite-related brain reward activity (via BOLD-fMRI with food cues). Exploratory analyses include conventional cardiometabolic risk markers (blood pressure, lipid and glucose metabolism), and perceivable (consumer) benefits.

Participants needed: 40
Trial details
Age: 40-75Biological sex: AllType: InterventionalSponsor: Maastricht University Medical CenterUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

Men and postmenopausal women (≥ 2 years since last menstruation); [+8]

Left-handedness; [+14]

Status: Recruiting

Lutein, Zeaxathin, and Fish Oil Supplementation

The goal of this clinical trial is to learn the impact of lutein, zeaxanthin, and fish oil (LZF) supplementation in healthy adults. The main question it aims to answer is: Will supplementation with LZF improve macular pigment optical density (MPOD), cognitive performance and bone mass compared to controls after six months? Subjects with an MPOD \<.43 will significantly improve MPOD after 6-months of LZF supplementation. Consuming a LZFO supplement for 6-months will improve visual cognitive performance. Consuming a LZFO supplement for 6-months will improve bone density. Participants will be asked to take either a LZF supplement or placebo daily for 6 months.

Participants needed: 80
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Texas A&M UniversityUpdated: Sep 30, 2025Locations: 1
Eligibility criteria

<.43 MPOD, a self-reported best-corrected vision of 20/40 or better in each eye,...

allergic to lutein, zeaxanthin, or fish oil, taking supplements with >6 mg lutei...

Status: Not yet recruiting

Exploring the Cognitive Benefits of a Blackcurrant-Based Supplement in Normobaric Hypoxia

This study investigates the cognitive effects of Ārepa, a blackcurrant-based drink, under simulated high-altitude conditions (4,500m normobaric hypoxia for \~180 minutes). Using a double-blind, randomised, placebo-controlled crossover design, participants will consume either the nootropic blackcurrant-based drink or a taste-matched placebo. Cognitive testing (\~80 minutes) includes Trail-making, Stroop, N-back, Serial 7s/3s, and RVIP tasks. Physiological measures (heart rate, SpO₂, blood) and biomarkers (MAO-B, BDNF, hsCRP, S100B, Prolactin, C3G, Sarmentosin) will be assessed. Scales will evaluate mood, wellbeing, and perceived effects. The aim is to determine if the nootropic drink can support cognitive function in hypoxic environments.

Participants needed: 27
Trial details
Age: 18-35Biological sex: MaleType: InterventionalSponsor: Leeds Beckett UniversityUpdated: Sep 10, 2025Locations: 1
Eligibility criteria

Willing and able to provide written informed consent (in English) [+3]

Diagnosed food allergy or intolerance to the investigational products or control... [+9]

Status: Recruiting

Use Muscadine Wine Nutraceuticals to Improve Brain Health, Cognition, and Mental Health

Previous studies have shown that polyphenol-rich foods can positively affect cognitive functions, memory, and mood in humans. We hypothesize that both acute and chronic intake of muscadine wine polyphenols will improve cognitive performance and mood through regulating the HPA axis, alleviating inflammation and oxidative stress, and/or inhibiting monoamine oxidase activities

Participants needed: 25
Trial details
Age: 50-65Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Jun 12, 2025Locations: 1
Eligibility criteria

Healthy [+2]

Pregnancy [+11]

Status: Recruiting

Peanut Consumption on Cognitive, Weight, and Inflammation

A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.

Participants needed: 200
Trial details
Age: 10-12Biological sex: AllType: InterventionalSponsor: University of BarcelonaUpdated: Apr 3, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Determining Which Regions of the Brain Are Active During Flight Simulation at Separate Timepoints During Training

The overall objective is to identify the cognitive circuits associated with military aviator performance by analyzing what anatomic regions of the brain are functionally "active" (neuronal circuit) while being performing virtual flight simulations, the Precision Instrument Control Task (PICT). The flight simulation test will be conducted at two separate timepoints while the subject is receiving a Functional Magnetic Resonance Imaging (fMRI) scan to evaluate which anatomic and functional brain function is associated with precise performance. By scanning at multiple time points we aim to quantify changes in functional and anatomic connectivity that occur throughout the course of training.

Participants needed: 150
Trial details
Age: 18-54Biological sex: AllType: InterventionalSponsor: The Geneva FoundationUpdated: Jan 15, 2025Locations: 1
Eligibility criteria

Active Duty Military Pilots (Instructor Pilot Trainees or Remote Piloted Aircraf... [+2]

Age < 18 years [+11]

Status: Recruiting

Clinical Study to Evaluate the Effects of Two Novel Hydration Beverage Formulas on Rehydration in Healthy Adults

The aim of the clinical trial is to evaluate the efficacy of two novel hydration products on rehydration following exercise.

Participants needed: 16
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Liquid I.V.Updated: Jul 29, 2024Locations: 1
Eligibility criteria

Healthy adult male and female participants who are between 18 and 49 years of ag...

Female participants who are lactating, pregnant or planning to become pregnant d...