Memory

18

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

Condition / disease
Location
Status: Recruiting

Cannabis Observations on Brain Waves, Retrieval, and Attention: Experiment 4

This study investigates the impact of ∆9-tetrahydrocannabinol (THC) and cannabidiol (CBD) on recognition memory in healthy, regular cannabis users. Participants complete the same recognition memory task after self-administering one of two different strains of cannabis flower one day and while not intoxicated another day. Event-related potentials (ERPs) are measured via electroencephalogram (EEG) during the recognition memory task. Blood is collected to quantify THC and CBD exposure. Participants also complete self-report measures of medical history, sleep quality, subjective cognitive function, physical activity, psychological functioning, substance use, and acute drug effects.

Participants needed: 64
Trial details
Age: 21-40Biological sex: AllType: ObservationalSponsor: L. Cinnamon BidwellUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Must be between the ages of 21 and 40 and provide informed consent; [+16]

Status: Recruiting

Longitudinal Investigation of Sleep, Memory, and Brain Development Across the Nap Transition

To examine the relations between sleep (nap transitions, sleep physiology), memory, and brain development longitudinally, the researchers will assess n=180 children (in order to acquire n=152 usable data sets) who are 36-54 months of age and habitual nappers at enrollment. In each wave, the researchers will assess memory, memory change over a nap and equivalent waking interval, sleep physiology of the nap, and brain structure and function (using Magnetic Resonance Imagining or MRI). Additionally, overnight sleep physiology will be assessed in all participants. Waves will take place approximately every 6 months. For all children, three waves will be collected. With these data, the researchers will address the following aims: * Examine neural markers that predict the sleep transition (Aim 1); * Examine changes in sleep-dependent memory processing (mnemonic discrimination) over both nap and overnight sleep intervals, across the sleep transition (Aim 2); * Examine changes in sleep microstructure in both nap and overnight sleep across the sleep transition (Aim 3) * Examine interrelations among brain, memory and sleep microstructure across the sleep transition (Aim 4)

Participants needed: 180
Trial details
Age: 36-60Biological sex: AllType: InterventionalSponsor: University of Maryland, College ParkUpdated: Jun 4, 2026Locations: 2
Eligibility criteria

36-60 months at the time of enrollment [+2]

diagnosis of any sleep disorder (other than mild parasomnia which is routine at... [+8]

Status: Not yet recruiting

Unconscious Mind Training

H22 - Unconscious Mind Training and Memory Encoding Phase I The core problem this clinical trial, H22, seeks to address is the pervasive challenge of modifying deeply ingrained, often unconscious, unwanted behaviors within the general population. Many individuals struggle with habits or actions that negatively impact quality of life, productivity, or well-being, yet conventional methods often fall short due to the unconscious nature of these behaviors. Specifically, the trial aims to investigate the efficacy of H22, a novel intervention designed to engage and train the unconscious mind, in mitigating these unwanted behaviors. The central hypothesis guiding this research is that H22 training will empower volunteers to significantly reduce the frequency and intensity of identified unwanted behaviors.

Participants needed: 100
Trial details
Age: 10-75Biological sex: AllType: InterventionalSponsor: Dream Video LLCUpdated: Jun 3, 2026
Eligibility criteria

Can read and write [+1]

Status: Not yet recruiting

Percepta for Cognitive Optimization

This Phase 1, randomized, double-blind, placebo-controlled trial evaluates the cognitive and neurophysiological effects of a dietary supplement containing cat's claw (Uncaria tomentosa) bark extract and oolong tea extract, in adults aged 40-85 with self-reported mild cognitive impairment (MCI). The study employs a decentralized design leveraging remote monitoring technologies. Participants will self-administer the study supplement or a matched placebo daily for 6 months. The primary outcome is cognitive performance assessed by digital Montreal Cognitive Assessment (MoCA) at baseline, Month 3, and Month 6. Secondary outcomes include objective sleep and autonomic metrics from Oura Ring wearables (heart rate variability, sleep architecture) and self-reported brain health using the Brain Health Index. An exploratory sub-study will measure plasma biomarkers of neurodegeneration (pTau-217) at baseline and Month 6 in a subset of participants to explore potential mechanisms of action. The study aims to provide preliminary evidence for Percepta's efficacy in improving cognitive function and supporting brain health in individuals with MCI, while evaluating safety and biological plausibility through mechanistic biomarkers.

Participants needed: 154
Trial details
Age: 40-85Biological sex: AllType: InterventionalSponsor: Cerebrum DAO AssociationUpdated: May 28, 2026Locations: 1
Eligibility criteria

Demographics: Must be English-speaking and currently residing in the United Stat... [+4]

Neurological and Psychiatric Disorders: A self-reported diagnosis of dementia, A... [+4]

Status: Not yet recruiting

Memory Enhancement in Aging With Optimal Dosing

This project optimizes high-resolution tACS to improve memory in healthy older adults, advancing drug-free approaches for ADRD. We test stimulation schedules and develop an adaptive, brain-guided tACS system to strengthen memory-supporting networks.

Participants needed: 240
Trial details
Phase: Early Phase 1Age: 65+Biological sex: AllType: InterventionalSponsor: Boston University Charles River CampusUpdated: Apr 7, 2026
Eligibility criteria

65 years of age or older [+2]

pregnant [+10]

Status: Recruiting

Synchronization of Theta to Influence Memory

This study aims to clarify relations between brain oscillations and two cognitive functions: cognitive control and memory.

Participants needed: 90
Trial details
Age: 18-59Biological sex: AllType: InterventionalSponsor: Florida International UniversityUpdated: Mar 17, 2026Locations: 1
Eligibility criteria

18 years and older [+3]

Must not have ever had an injury to the head that's caused you to be knocked out... [+18]

Status: Not yet recruiting

Non-Invasive Detection and Preservation of Neurocognitive Signals in the Peri-Death Period Using Brain-Computer Interface and Artificial Intelligence

Background: Recent electroencephalography (EEG) data indicate that the transition from clinical death to cellular death is marked by highly organized neurophysiological events, including significant surges in gamma-band power, cross-frequency coupling, and distinct spreading depolarization waves. This prospective, observational feasibility study utilizes rapid-deployment, high-density, noninvasive BCI hardware paired with proprietary AI analytics to detect, classify, and securely archive these terminal neurocognitive signals. Objectives: (1) Quantify transient gamma-band activity and cross-frequency connectivity post-clinical death; (2) Validate the efficacy of machine learning models for real-time signal classification in high-noise clinical environments; (3) Establish a highly secure, encrypted bio-informational archive of peri-life EEG data. Design: Prospective, open-label, multicenter, observational cohort (n\>20).

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Noah Tech, Corp.Updated: Mar 17, 2026
Eligibility criteria

Adults ≥18 years with terminal illness or severe acute trauma [+3]

Brain death already declared > 24 hours prior to enrollment [+2]

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: Recruiting

Prediction of Anxiety and Memory State

The purpose of this study is to look at how signals in the brain, body, and behavior relate to anxiety and memory function. This project seeks to develop the CAMERA (Context-Aware Multimodal Ecological Research and Assessment) platform, a state-of-the-art open multimodal hardware/software system for measuring human brain-behavior relationships. The R61 portion of the project is designed to develop the CAMERA platform, which will use multimodal, passive sensor data to predict anxiety-memory state in patients undergoing inpatient monitoring with intracranial electrodes for clinical epilepsy, as well as to build CAMERA's passive data framework and active data framework.

Participants needed: 40
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Columbia UniversityUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

Patients must have known or suspected Temporal Lobe Epilepsy. [+3]

Hearing impaired (i.e., not corrected with a hearing aid) [+8]

Status: Recruiting

Effects of Exercise and Sleep on Motor Learning and Functional Abilities in Multiple Sclerosis

The ExSiMS study is a randomized, controlled crossover study including 20 individuals (18-70 years) diagnosed with relapsing remitting Multiple Sclerosis (MS) This project investigates, through behavioral and neurophysiological measurements, how aerobic exercise on an ergometer bike and sleep in the form of a nap and overnight sleep may enhance cortical motor skill learning evaluated by a complex hand motor skill test and thereby improve functional capacity in individuals with MS. Beyond the effect on motor skill learning, the project investigate the effect on electroencephalography (EEG) - electromyography (EMG) coherence. The study hypothesizes that individuals with neurological conditions, such as multiple sclerosis (MS), may experience beneficial effects on specific motor rehabilitation through systematically planned cardiovascular exercise and sleep scheduling, due to positive impacts on memory consolidation. Aims: * Investigate the brain's neurophysiological responses and memory effects following a training intervention and, separately, sleep, in the form of a power nap, in individuals with MS. * Examine whether these effects persist beyond the few days previously observed in healthy individuals by implementing a longer-term intervention. * Explore whether the training effect is influenced by disease activity in the brain, such as during relapses and during immunosuppressive treatment. * Assess whether the presence of abnormally reduced cognitive endurance (fatigue) affects the impact of the intervention involving exercise and sleep. The study is based on documented positive effects of physical activity and sleep in both young and older adults, as well as in individuals recovering from stroke. The research thus offers promising perspectives for broader applications within neurorehabilitation, and particularly for MS, as the disease is associated with functional impairments. At the same time, both physical exercise and sleep represent meaningful interventions that should be thoughtfully integrated into rehabilitation strategies.

Participants needed: 20
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Zealand University HospitalUpdated: Jan 8, 2026Locations: 2
Eligibility criteria

Competent individuals (aged 18-70) diagnosed with early relapsing-remitting MS [+2]

Implanted devices, such as pacemakers or stimulators [+1]

Status: Recruiting

Virtual Contexts for Affective Modulation

This study investigates how spatial context and perceived controllability modulate pain, affective states such as anxiety, and motivated behavior. The study examines how control over pain and threat-related environments influences pain perception, state anxiety, associated autonomic responses, and behavior. The main questions it aims to answer are: Does having control over pain within specific contexts alter how much pain people feel-even when the stimulus intensity remains constant? How do different types of environments (safe, controllable, or uncontrollable) shape pain-related brain activity, subjective anxiety, and physiological arousal? How do people perform cognitively demanding or distracting tasks (and retain their memory) when under threat versus when in control? Lastly, how do these learned associations with spatial contexts persist or adapt when environmental contingencies are explicitly changed? Taken together, exploration of these factors may lay the groundwork for understanding how placebo-related mechanisms-including perceived control, contextual learning, emotional engagement, and distraction-interact to shape pain and anxiety in complex environments.

Participants needed: 20
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Trustees of Dartmouth CollegeUpdated: Oct 31, 2025Locations: 1
Eligibility criteria

No self-reported current or history of depression, bipolar disorder, or other ps... [+9]

Status: Recruiting

Cognitive Vitality Pilot Study

This study's purpose is to evaluate the effects of a dietary supplement on cognitive function and psychological well-being in community-dwelling older adults aged 55+. The study involves taking a commercially available dietary supplement daily for 45 days. A 45-minute assessment will be conducted at the beginning and again at the end of the study.

Participants needed: 16
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: Arizona State UniversityUpdated: Oct 28, 2025Locations: 1
Eligibility criteria

Adults aged 55 years and older [+8]

Previous participation in a cognitive dietary supplement study in the last 12 mo... [+12]

Status: Recruiting

Remediation Program Via a "Serious Game" for the Cognitive Functions of Multiple Sclerosis Patients

The main goal of this study is to assess the effectiveness of a cognitive remediation program based on a "serious game" on the information processing speed evolution and the process of learning via episodic memory in multiple sclerosis patients.

Participants needed: 150
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Lille Catholic UniversityUpdated: Sep 4, 2025Locations: 6
Eligibility criteria

Relapsing-remitting or progressive multiple sclerosis people defined according t... [+7]

Severe cognitive deficit defined by obtaining a deficit score in more than six c... [+8]

Status: Recruiting

MRI Neurofeedback and Brain Circuits Related to Motivation in Healthy Participants

The purpose of this research study is to understand how healthy individuals self-regulate motivation by observing brain activity using magnetic resonance imaging (MRI).

Participants needed: 190
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Duke UniversityUpdated: Aug 22, 2025Locations: 1
Eligibility criteria

Age between 18 and 45 years [+4]

Current or diagnosis within past six months of an DSM-V Axis I or Axis II disord... [+19]

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: Not yet recruiting

Adaptation and Normalization of a Verbal Episodic Memory Test in French Sign Language

To date, neuropsychological assessment of deaf signing persons is complicated by a lack of resources, especially the absence of tools available in French Sign Language (LSF). This is due to perceptual and cultural differences, and in particular the linguistic differences between French and LSF. This lack of resources significantly hinders access to care for deaf patients, as neuropsychological assessment is often a key clinical criterion in the diagnosis of certain neurological pathologies (Alzheimer's disease in particular) and enables coherent care plans to be drawn up, for example in the aftermath of strokes or traumatic brain injuries. In particular, episodic memory (which refers to the ability to memorise information anchored in a specific context) is a cognitive domain that is sensitive to pathologies such as Alzheimer's disease, but it is not currently possible to assess it with deaf signing patients. The aim of this study is to create a memory assessment test adapted to a deaf population that expresses in LSF and to normalize this test on this same population. The aim is to provide a diagnosis assessment tool, which currently does not exist in France, to improve access to care for deaf people. This project could then be extended to the creation of tests for other cognitive domains (executive functions, attention, social cognition, etc.) and to prospects for cognitive remediation. The 16-item Free and Cued Recall test (RL-RI 16) is the best choice because it is easy to use and accurate enough to assess each stage of episodic memory. These qualities make it a decisive tool in certain differential diagnosis. In order to select the most relevant signs, lexical lists by frequency in LSF will be drawn up during a preliminary phase, during which the participants will have to give, in one minute, the maximum number of signs belonging to different categories (animals, vegetables, clothes...). These lists will be used to select the most relevant signs according to their frequency (neither too common nor too rare), based on the same principle as RL-RI 16. It will then be standardised on deaf adults, for whom LSF is the main language, with no cognitive impairment, across France, via the various Deaf Care Units, with the help of French / LSF interpreters. Working with different centers in France will make it possible to recruit a larger and more representative number of participants, and to be more sensitive to any regional effects.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Poitiers University HospitalUpdated: Mar 30, 2025
Eligibility criteria

Person aged ≥ 18 yo [+11]

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: Mar 21, 2025Locations: 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

Home Sleep Therapy for Older Adults With MCI

The goal of this clinical trial is to learn about the ability of non-invasive brain stimulation during sleep to enhance people's deep sleep and its potential benefit on memory in people with mild cognitive impairment via home use sleep therapy device (SleepWISP) as well as learn about biomarkers associated with Alzheimer disease (AD). The clinical trial aims to answer the following main questions: 1. Whether the non-invasive transcranial electrical stimulation (TES) delivered by SleepWISP could provide short-term enhancement of deep sleep in a single night in the target population. 2. Whether TES delivered by SleepWISP could enhance deep sleep over multiple nights in the target population. 3. Whether enhance on deep sleep could improve memory performance in the target population. Participants will be asked to wear non-invasive and painless devices that record their brain activity during sleep along with an actigraphy watch that measures their movement throughout the day. In addition, blood samples or nasal swab assays will be collected from participants multiple times during the study.

Participants needed: 60
Trial details
Age: 40-85Biological sex: AllType: InterventionalSponsor: Brain Electrophysiology Laboratory CompanyUpdated: Feb 17, 2025Locations: 2
Eligibility criteria

For participant with Amnestic MCI, the inclusion age range is 55-85 years old. [+1]

History of seizures [+14]