Cognitive Function

37

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

Condition / disease
Location
Status: Not yet recruiting

PACE Cognition Proof-of-Concept Study

This proof-of-concept study will evaluate whether physiologic pacemaker programming improves cognitive function and health status in patients with symptomatic bradycardia who require permanent pacemaker implantation. Participants will be randomized to either standard pacemaker programming at 60 beats per minute or individualized physiologic rate pacing between 60 and 90 beats per minute using the myPACE algorithm. Cognitive function and health status will be assessed before pacemaker implantation and again at the routine 3-month pacemaker clinic visit. The primary outcome is change in Montreal Cognitive Assessment total score. The secondary outcome is change in SF-36 mental component summary score.

Participants needed: 110
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MinnesotaUpdated: Oct 7, 2026Locations: 2
Eligibility criteria

Vulnerable adult unable to give consent [+9]

Status: Recruiting

Association Between Sleep Quality and Self-Care in Heart Failure Patients

The research will be conducted as a prospective and relational study to longitudinally investigate the effect of sleep quality on self-care in patients with heart failure (HF) and to evaluate the relationship between self-care, sleep quality, and cognitive functions. The sample size was calculated using the multiple linear regression model with the G\*Power Version 3.1 program. Based on a medium effect size of 0.15, an alpha of 0.05, a power of 0.95, and 18 predictors, the sample size was determined to be 188. Considering a potential dropout rate of 10%, it was decided to complete the study with a minimum of 207 participants. Data will be collected from patients who apply to the Dokuz Eylül University Cardiology Outpatient Clinic and meet the inclusion criteria. After signing the informed consent form, participants will be followed up at baseline, the 1st month, the 3rd month, and the 6th month by telephone. The Statistical Package for Social Sciences (SPSS) 24.0 will be used to analyze the numerical data of the research. Descriptive statistics, including number, percentage, mean, and standard deviation, as well as inferential statistics such as the χ2 test, t-test for independent groups, and multiple linear regression, will be employed in the data analysis.

Participants needed: 207
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dokuz Eylul UniversityUpdated: Oct 7, 2026Locations: 1Duration: 6 Months
Eligibility criteria

Are diagnosed with heart failure according to international guidelines, [+3]

Have been hospitalized within one month prior to inclusion, [+6]

Status: Recruiting

IMST for Dementia Risk Reduction

Using a 2-arm, RCT approach, the primary goal of the study is to evaluate the feasibility and preliminary efficacy of Inspiratory Muscle Strength Training (IMST) as a non-pharmacologic intervention to reduce cardiovascular and cognitive risks in older adults. Next, investigators will examine secondary effects of IMST on mood, sleep quality, systemic inflammation, and physical/motor function. Finally, investigators will assess participant adherence and acceptability ratings of using an 8-week home-based IMST protocol in a diverse older adult sample.

Participants needed: 30
Trial details
Age: 60-80Biological sex: AllType: InterventionalSponsor: Florida State UniversityUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Ages 60-80 [+5]

tMoCA <18, or diagnosis of neurodegenerative illness at the discretion of princi... [+8]

Status: Not yet recruiting

A Virtual Clinical Trial to Examine the Effect of Magnesium Choline Citrate on Cognitive Function and Anxiety in Healthy Adolescents and Adults

The goal of this clinical trial is to examine the effect of Magnesium Choline Citrate on cognitive function and anxiety in healthy adolescents and adults. The main questions it aims to answer are: * What is the change in cognitive function, as assessed by the PROMIS Cognitive Function- Short Form 8a (≥18 years old) from baseline to Day 84 between Magnesium Choline Citrate and placebo? * What is the change in cognitive function, as assessed by the Pediatric Cognitive Function - Short Form 7a (9 - 17 years old) from baseline to Day 84 between Magnesium Choline Citrate and placebo? Researchers will compare Magnesium Choline Citrate with placebo to evaluate its effects on cognitive function and anxiety symptoms. Participants will be asked to: * Consume either Magnesium Choline Citrate or placebo for 84 days * Complete questionnaires (PROMIS Cognitive Function- Short Form 8a/Pediatric Cognitive Function - Short Form 7a, and PROMIS Emotional Distress - Anxiety - Short Form 8a/Pediatric Anxiety - Short Form 8a) * Complete a study diary weekly

Participants needed: 200
Trial details
Age: 9+Biological sex: AllType: InterventionalSponsor: Nutrisol, LLCUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Males and females 9 years and older [+9]

Individuals who self-report as pregnant, breast feeding, or planning to become p... [+18]

Status: Recruiting

Multi-level Approach of Brain Activity Using Intracranial Electrodes in Epileptic Patients

The main goal of this project is to study the mechanisms of epileptic activities using intracranial macro and micro electrodes in epileptic patients undergoing pre-surgical investigation. The recordings will also be used to study physiological mechanisms like sleep and different cognitive functions.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Institut National de la Santé Et de la Recherche Médicale, FranceUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

Patients with focal drug-resistant epilepsy [+2]

Contraindication for an intracranial investigation (with macro-electrodes) : int... [+3]

Status: Recruiting

A Clinical Trial to Investigate the Safety and Efficacy of AP-Brain on Cognitive Function at Varying Dosages in Healthy Younger Adults With Self-reported Attention Problems

The goal of this clinical trial is to investigate the safety and efficacy of AP-Brain on cognitive function at varying dosages in healthy younger adults with self-reported attention problems. The main question it aims to answer is what Change from baseline to Day 56 between AP-Brain (1g, 3g, or 5g) and placebo in cognitive function, as assessed by the CNS VS Neurocognitive Index (NCI) score and complex attention. 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: 18-39Biological sex: AllType: InterventionalSponsor: Rousselot BVBAUpdated: Sep 18, 2026Locations: 2
Eligibility criteria

Males and females 18-39 years of age, inclusive [+16]

Individuals who are pregnant, breast feeding, or planning to become pregnant dur... [+31]

Status: Recruiting

The Impact of Omega-3 Fatty Acid Supplementation on the Composition of Erythrocyte Membranes in Athletes

The aim of this study is to evaluate the effects of omega-3 fatty acid supplementation on the Omega-3 Index, erythrocyte membrane composition, cognitive function, hormonal profile, speed, endurance performance, and hematological parameters in competitive athletes aged 16-35 years.

Participants needed: 200
Trial details
Age: 16-35Biological sex: AllType: InterventionalSponsor: The Jerzy Kukuczka Academy of Physical Education in KatowiceUpdated: Aug 17, 2026Locations: 1
Eligibility criteria

Male competitive soccer players aged 16-35 years. [+7]

Current use of omega-3 fatty acid supplements or fish-oil products. [+9]

Status: Not yet recruiting

Montessori-Based Interventions for Older Adults

The aim of this study is to evaluate the effect of Montessori-based interventions on cognitive function and activities of daily living in older adults.

Participants needed: 60
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Gazi UniversityUpdated: Aug 11, 2026Locations: 1
Eligibility criteria

Being 65 years of age or older [+2]

Having a history of severe orthopedic or neurological disorders (e.g., stroke, P... [+2]

Status: Recruiting

Binaural Beats for Cognitive Function in Older Adults With Mild Cognitive Impairment in Nursing Homes

This study will evaluate whether binaural beats can improve cognitive function in older adults with mild cognitive impairment living in nursing homes. Participants will listen to 10-Hz alpha-frequency binaural beats through headphones once daily for 30 minutes for 14 consecutive days. Cognitive function, sleep quality, anxiety, and depressive symptoms will be assessed before the intervention, after the intervention, and at a 2-week follow-up after the intervention. The study aims to determine whether binaural beats are a safe, simple, and non-drug approach to support cognitive health in older adults with mild cognitive impairment.

Participants needed: 60
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: China Medical University, ChinaUpdated: Jul 30, 2026Locations: 3
Eligibility criteria

Age 60 years or older. [+6]

Severe physical disease, major organ failure, or advanced malignant tumor. [+6]

Status: Recruiting

Effect of Daily Mixed Spice Consumption on Memory Function

The aging process entails a multitude of structural and functional alterations within the brain, culminating in a gradual and progressive decline in cognitive function. Recent research has indicated that various spices may hold the key to enhancing brain health and combating the effects of aging on cognitive abilities. The hypothesis is that a mixture of spices, acknowledged for their reported memory protection potential, may yield a more potent beneficial effect on memory function than a single spice. The spice mixture will be used at culinary dose, and therefore side effects are anticipated. In this study, the effects of spice mixture will be evaluated, as well as their anti-oxidant, and anti-inflammatory properties. The proposed pilot study will include 50 adults (ages 50-80), exhibiting typical age-related mild cognitive decline, excluding dementia or major neurocognitive disorders. They will be randomized 1:1 assigned into a daily intake of either 4.00 g spice mixture capsules or 4.00 g maltodextrin capsules over 3 months, and explore the sustainable effect over 3 additional months. The changes in symptoms of cognition, fatigue, and mood symptoms of the spice group vs. placebo group will be compared. The outcome of the investigation of the effects of mixed spice consumption will provide important novel information on dietary recommendation of spice to preserve cognitive function in aging population.

Participants needed: 50
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: University of California, Los AngelesUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

Participants are required to have clinical histories consistent with normal agin... [+3]

Diagnosis of probable Alzheimer's disease or any other dementia (e.g. vascular,... [+9]

Status: Recruiting

Diet, Metabolic Health, and Exercise Responses

Regular physical activity, healthy dietary habits, and good metabolic health are associated with numerous physical and cognitive health benefits. However, individuals vary substantially in their affective, motivational, and cognitive responses to exercise, and the factors contributing to this variability are not fully understood. This prospective observational study will examine whether habitual dietary fat quality and metabolic health are associated with exercise responses, cognitive function, and academic-related outcomes in healthy young adults. Participants will complete assessments of dietary intake, body composition, metabolic health, aerobic fitness, cognitive function, and academic engagement. They will also complete a standardized moderate-intensity cycling session during which affective responses, exercise enjoyment, subjective energy, and motivation for future physical activity will be assessed. The findings will improve understanding of how habitual dietary habits and metabolic health may influence responses to exercise and cognitive functioning and may help inform future lifestyle recommendations aimed at promoting physical activity participation, cognitive performance, and overall health.

Participants needed: 100
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: University of Wisconsin, River FallsUpdated: Jul 27, 2026Locations: 1
Eligibility criteria

Age 18 years or older. [+4]

Known cardiovascular, pulmonary, metabolic, neurological, psychiatric, or other... [+9]

Status: Recruiting

Brain Health in Breast Cancer Survivors

Endocrine therapy (ET) is widely used to treat hormone receptor positive breast cancer and prevent recurrence by downregulating estrogen function. However, ETs readily cross the blood brain barrier and interfere with the action of estrogen in the brain. Estrogen supports cognition and menopausal status is closely linked to cognitive health in women. This has raised concern that anti-estrogen ETs may affect cognition and brain health in breast cancer survivors. However, evidence across existing studies is inconsistent and these effects remain poorly understood. The incomplete understanding of the effects of ET are likely due to limitations of earlier studies - namely, the under-appreciation of the role of menopausal status and insensitivity of standard cognitive measures. This research project will address these earlier limitations by specifically comparing ET effects by menopausal status, and using highly sensitive, task-related functional magnetic resonance imaging (fMRI) measures to assess the effects of ET on brain function.

Participants needed: 120
Trial details
Age: 35-65Biological sex: FemaleType: ObservationalSponsor: Jonsson Comprehensive Cancer CenterUpdated: Jul 7, 2026Locations: 1
Eligibility criteria

Age 35-65 [+2]

History of major or mild neurocognitive disorder or dementia [+12]

Status: Not yet recruiting

Radicle Energy VBMTM: A Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes

Radicle Energy VBMTM: A randomized, double-blind, placebo- controlled direct-to-consumer study assessing the impact of health and wellness products on fatigue and related health outcomes.

Participants needed: 550
Trial details
Age: 21-105Biological sex: AllType: InterventionalSponsor: Radicle ScienceUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Adults, at least 21 years of age at the time of electronic consent, inclusive of... [+17]

Status: Recruiting

Exploring Virtual Reality Adventure Training Exergaming

The current project aims to design and implement an 8-week Virtual Reality Adventure Therapy Exergaming (V-RATE) intervention focused on women veterans. A randomized controlled trial using a repeated measure design with a 1-month follow-up assessment will be employed to examine effects on physical and mental health outcomes.

Participants needed: 40
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: The University of Texas at ArlingtonUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Are between the ages of 18 and 45 [+1]

Unable to walk independently (e.g., use of any mobility assistive device such as... [+6]

Status: Not yet recruiting

Mobile Dual-Task Brain and Balance Intervention for Concussion Recovery

This research study examines recovery after a sports-related concussion or mild head injury. Many athletes experience lingering problems with thinking, balance, and mood months after a concussion. We are testing a new home-based program called BraW-Day™ (Brain \& Walk Exercise Every Day). This 14-day program uses a mobile app on your smartphone and combines simple brain exercises (like counting backwards) with walking exercises. The idea is that doing these tasks together may help your brain and body recover more effectively. What You'll Do: * Two in-person visits at UNLV (baseline and after 14 days) for assessments * Daily 15-minute exercises at home using the BraW-Day app * Provide a small saliva sample for biomarker testing * Complete brief questionnaires about your symptoms and health Potential Benefits: You may experience improvements in thinking, balance, or mood. Even if you don't benefit directly, your participation will help researchers understand how to better support athletes recovering from concussion. Who Can Join: * Ages 18-40 * Had a sports-related concussion or mild head injury within the past 3-12 months * Have a smartphone and can safely do light walking and simple tasks This study is registered at ClinicalTrials.gov and approved by the UNLV Institutional Review Board to protect your safety and rights.

Participants needed: 20
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Hyunhwa LeeUpdated: May 20, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 40 years [+6]

Age younger than 18 years or older than 40 years [+7]

Status: Recruiting

Gait and Cognitive Function in Relation to Foot Arch Structure in Older Adults

This study aims to investigate the relationship between foot arch structure and spatiotemporal gait parameters and cognitive function in older adults. Foot arch integrity will be assessed using the Navicular Drop Test, and gait performance will be evaluated using the 10-Meter Walk Test. Cognitive-motor interaction will be examined through lower extremity reaction time using a light-based system. The study is designed as an observational cross-sectional analysis.

Participants needed: 50
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Balikesir UniversityUpdated: May 12, 2026Locations: 1
Eligibility criteria

Aged 65 years or older [+3]

Diagnosed neurological disorders affecting gait and motor control (e.g., stroke,... [+4]

Status: Not yet recruiting

Long-term Follow-up of Dexmedetomidine-esketamine and tDCS for Neurocognitive Complications After Surgery

Neurocognitive complications, mainly delirium and neurocognitive disorders, are common cerebral complications in older patients after surgery and associated with worse long-term outcomes. An ongoing 2×2 factorial trial conducted by the investigators plan to test the effects of perioperative dexmedetomidine-esketamine combination and transcranial direct current stimulation (tDCS) on postoperative neurocognitive complications in older patients. This long-term follow-up of the ongoing trial aims to investigate the effects of perioperative dexmedetomidine-esketamine combination and tDCS on long-term outcomes in older patients after noncardiac surgery.

Participants needed: 1,160
Trial details
Phase: Phase 4Age: 65-90Biological sex: AllType: InterventionalSponsor: Peking University First HospitalUpdated: May 12, 2026Locations: 6
Eligibility criteria

Aged 65 to 90 years; [+3]

Preoperative inability to communicate due to coma, severe dementia, endstage dis... [+8]

Status: Recruiting

Brain Stimulation Effects on Cognitive Task Performance

The purpose of this study is to determine optimal task design parameters for the measurement of transcranial magnetic stimulation (TMS) effects on cognition.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Colorado State UniversityUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

Right-handed [+1]

History of seizures or epilepsy [+21]

Status: Recruiting

Investigation of Motor Imagery Ability, Body Awareness and Cognitive Functions in Type 2 Diabetes Mellitus

The aim of this study is to examine the relationship between motor imagery skills, body awareness and cognitive functions in individuals with Type 2 Diabetes mellitus.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Being a type 2 DM patient between the ages of 18-65 for at least 5 years, [+2]

Having previous experience with Motor Imagery techniques or training, [+3]

Status: Recruiting

Effect on Body Movement and Mental Skills in Patients Who Received Gadolinium-based Contrast Media for Magnetic Resonance Examination Multiple Times Within 5 Years

This study is a postmarketing requirement jointly carried out by four NDA holders (Bayer AG, Bracco, GE Healthcare and Guerbet) and the CRO IQVIA. The study aims to create detailed images of the organs and tissue of the human body during x-ray, CT-scan or MRI investigations, doctors are using contrast media (a kind of dye) which can be given to patients by injection into a blood vessel or by mouth. In this study researchers want to find out whether so called gadolinium-based contrast agents (GBCAs) have an effect on body movement and mental skills when given to participants multiple times within 5 years. The study plans to enroll about 2076 participants suffering from a condition for which they are likely to have at least annually a MRI or another imaging examinations. Only adults up to 65 years will be considered to join this study. During the study duration of 5 years participants will receive annually a MRI or other imaging tests (such as CT-scan, x-ray) and will visit the study doctor at least 7 times for physical examinations, laboratory investigations and tests on body movement and mental skills.

Participants needed: 2,076
Trial details
Phase: Phase 4Age: 18-64Biological sex: AllType: InterventionalSponsor: GuerbetUpdated: Jan 22, 2026Locations: 51
Eligibility criteria

Participant must be neurologically normal, defined as free of unstable neurologi... [+6]

As evidenced by history or determined in the neurologic exam at screening, concu... [+11]

Status: Recruiting

B-vitamins and Omega-3 Fatty Acids and Biomarkers of Brain Atrophy.

A poor nutrition status is a modifiable risk factor for cognitive decline and dementia. In particular, evidence links low status of certain B-vitamins and ω-3 fatty acids (ω-3 FA) with a greater risk of cognitive decline and dementia. Although these dietary components are typically investigated separately, post-hoc analyses of existing clinical trial data and experimental work indicate that B-vitamins and ω-3 FA may exert synergistic beneficial effects on processes related to brain health and cognition. However, this combination has not been tested directly in humans. In the proposed BOOMERANG project, we will study the effects of jointly supplementing with B-vitamins and a highly bioavailable ω-3 FA supplement, Lysoveta, on a robust biomarker of brain atrophy, the neurofilament light chain, in a double-blinded randomized controlled trial (RCT) over 3 months in older adults. We will also examine the secondary effects of the supplement of quality of life and cognitive function.

Participants needed: 96
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: University of OsloUpdated: Dec 31, 2025Locations: 1
Eligibility criteria

Age > 65 years [+2]

Unable to give informed consent [+9]

Status: Not yet recruiting

Oral Nutritional Supplementation in Children With Growth Concerns

Multi-center, single-blinded, randomized, controlled study consisting of two arms, to investigate the impact of an oral nutritional supplement in combination with dietary counseling on growth in children with growth concerns as compared to children who receive dietary counselling alone

Participants needed: 216
Trial details
Age: 24-41Biological sex: AllType: InterventionalSponsor: Société des Produits Nestlé (SPN)Updated: Dec 31, 2025
Eligibility criteria

Child's parent(s) is of legal age of majority (18 years of age), must understand... [+7]

Child is currently breastfed or is consuming breast milk. [+13]

Status: Recruiting

Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators

The purpose of this study is to evaluate the dose-dependent effects of glucosyl-hesperidin (CITRAPEAK) supplementation on exercise performance, recovery indicators, blood flow, cognitive function, mood, sleep, and fuel utilization in recreationally active adults.

Participants needed: 60
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Lindenwood UniversityUpdated: Dec 12, 2025Locations: 1
Eligibility criteria

Participants who are between 18 - 50 years of age [+7]

Not currently completing at least 180 minutes of moderate to vigorous exercise p... [+19]

Status: Not yet recruiting

Time Restricted Eating in Survivors Trial 2.0

After chemotherapy, older breast cancer survivors experience a faster decline in brain function. This can make it harder to enjoy life, stay social, and maintain independence. Chemotherapy can lead to poorer lifestyle habits, like unhealthy eating, less exercise, high stress, and poor sleep. Chemotherapy can also affect important health markers like blood sugar and cholesterol. Over time, these changes can damage blood vessels, which might lead to heart and brain issues. The investigators do not fully understand why brain function declines faster after chemotherapy, especially in older survivors, because there are many factors involved. In this study, the investigators will look at how lifestyle habits (like diet, exercise, stress and sleep), health markers (like blood sugar and cholesterol), and blood vessel health (like how well blood flows and how stiff the blood vessels are) affect brain function in older breast cancer survivors. The investigators will include 152 females aged 60-85 years, who finished chemotherapy for early-stage breast cancer at least 1 year ago. The investigators will use special tests to check different parts of brain function, like language, memory, and attention, as well as brain blood vessel health. This will help to understand which factors might speed up or slow down memory and thinking problems. Since many Canadian breast cancer survivors experience faster decline in brain function after chemotherapy, this study aims to find out what might make it worse. The results could help to create better and more personalized treatment plans for older breast cancer survivors that protect brain health and reduce problems with brain function in the future.

Participants needed: 152
Trial details
Age: 60-85Biological sex: FemaleType: InterventionalSponsor: University of TorontoUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

female [+5]

does not have a mobile device that connects to Bluetooth and can send/receive te... [+14]

Status: Not yet recruiting

Exploring the Effectiveness of Somatosensory Cognitive Game Intervention on Cognitive and Physical Functions

This study investigates the effects of somatosensory cognitive games interventions on older adults' cognitive and physical functions. The investigators plan to recruit up to 100 participants and randomly assign them to a control group or an experimental group. The experimental group will participate in somatosensory cognitive games for 12 weeks, while the control group will receive routine care. Data will be collected via questionnaires to examine whether somatosensory cognitive games can delay declines in cognitive and physical functions in older adults.

Participants needed: 80
Trial details
Age: 65-100Biological sex: AllType: InterventionalSponsor: Taipei Medical UniversityUpdated: Nov 26, 2025
Eligibility criteria

Elderly individuals aged 65 and above. [+2]

Individuals with severe visual impairments or physical mobility disabilities tha... [+1]