Working Memory

9

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

Condition / disease
Location
Status: Recruiting

NIMH K23: Modulation of Frontoparietal Dynamics in Adolescent Working Memory Deficits

Working memory (WM) deficits are a transdiagnostic feature of adolescent psychopathology that substantially contribute to poor clinical and functional outcomes. This proposal will utilize a multimodal neuroscientific approach to investigate whether non-invasive brain stimulation can modulate the neural mechanisms underlying adolescent WM deficits. Directly in line with NIMH priorities, the researchers will identify the contributing roles of prefrontal and parietal regions in WM processes, as well as identify optimal targets and parameters for novel brain-based treatments in adolescent psychopathology. This study is funded by the NIMH-K23

Participants needed: 40
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Bradley HospitalUpdated: May 1, 2026Locations: 1
Eligibility criteria

Ability to provide assent and have parent provide parental permission [+5]

Intracranial pathology from a known genetic disorder (e.g., NF1, tuberous sclero... [+22]

Status: Recruiting

BID WM Digital Intervention in Aging

The goal of this clinical trial is to learn if engaging with an digital intervention may improve cognitive function. The main questions it aims to answer are: 1. Does engagement in with a digital intervention improve working memory? 2. Does engagement in with a digital intervention improve inhibitory control? Researchers will compare two different digital interventions to assess whether they may be helpful in improving cognitive function. Participants will conduct study activities remotely (e.g., at-home): 1. Baseline Assessment. Complete a series of cognitive assessments and surveys. 2. Intervention. Engage in a digital intervention for up to 8 weeks. 3. Post Intervention Assessment. Complete the same cognitive assessments and surveys as the Baseline Assessment. 4. Follow-Up Assessment. Six months after the intervention ends, participants will complete the same cognitive assessments and surveys as the Baseline Assessment.

Participants needed: 150
Trial details
Age: 60-85Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Minimum of 12 years of education [+4]

Under the age of 60 [+5]

Status: Recruiting

Modulation of Brain Oscillations Underlying Working Memory

This study will use novel transcranial alternating current stimulation (tACS) protocols and electroencephalography (EEG) to modulate and measure brain oscillations that underlie working memory. tACS is a noninvasive method used to modulate the timing and patterns of brain rhythms via weak electric currents passed through electrodes on the scalp.

Participants needed: 32
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

Able to provide informed consent [+1]

History of a neurological/psychiatric disorder [+3]

Status: Recruiting

Evaluation of the Impact of a Nutritional Formulation on Cognitive Performance Following Stress Exposure.

The proposed project will evaluate the synergistic effects of a nutritional formulation, 'Think Tank' on cognitive performance following exposure to a psychological and physical stressor. Adopting a double-blind repeated measures cross-over design, middle-aged females (40-60 years) will be recruited to take part in a two-stage research study that will examine whether the formulation enhances cognitive performance and subjective well-being following the challenge of a stressor, compared to placebo. Cognitive assessments will examine the impact of the nutritional formulation on working memory, sustained attention, cognitive flexibility and inhibitory control. The study will also assess physiological (heart rate, blood pressure and cortisol) and subjective (well-being, anxiety, positive and negative mood, stress) markers of stress reactivity. The study will also explore levels sleep quality, mental and physical fatigue, effort, productivity, and perceived impact of the intervention.

Participants needed: 40
Trial details
Age: 40-60Biological sex: FemaleType: InterventionalSponsor: Leeds Beckett UniversityUpdated: Jan 6, 2026Locations: 1
Eligibility criteria

Willing and able to provide written informed consent (in English) [+4]

Current cigarette smokers/vapers. [+13]

Status: Recruiting

Cross-over Study on the Influence of Fampridine on Working Memory in Mild to Moderate Depression

Cognitive deficits, including working memory deficits, are often present in depression and there are currently no effective pharmacological treatments targeting working memory deficits. Papassotiropoulos et al. (2024) has recently demonstrated that fampridine, a potassium channel blocker, can enhance working memory in healthy individuals with lower baseline performance, suggesting it may hold potential for addressing cognitive deficits in clinical populations. The primary aim of this study is to evaluate whether fampridine improves working memory performance in mild to moderate depression

Participants needed: 38
Trial details
Phase: Phase 2Age: 18-55Biological sex: AllType: InterventionalSponsor: University of BaselUpdated: Dec 12, 2025Locations: 1
Eligibility criteria

Male or female [+6]

Contraindications to the class of drugs under study, e.g. known hypersensitivity... [+23]

Status: Recruiting

Theories of Working Memory and Consolidation/RECOnsolidation in the Process of Resorption of Post-traumatic Symptoms.

EMDR is a psychotherapeutic approach recommended by the World Health Organization (WHO) for the treatment of disorders such as post-traumatic stress disorder, anxiety, depression and, more generally, psychological distress. In all these disorders, intrusions are one of the symptoms leading to intense emotional distress. EMDR therapy, by making intrusions less emotional and less present in the mind (i.e. less vivid), would reduce psychological distress. This symptomatological reduction would be made possible by the therapist's application of alternating bilateral visual (rapid eye movements following a point from left to right), auditory (tones emitted alternately in the right ear and then in the left ear) and/or tactile (tapping with fingers on the left and right shoulders alternately) stimulations administered while the patient concentrates on his or her intrusive thoughts. Accordingly, the aim of this research is to investigate the efficacy of self-administration of Alternating Bilateral Stimulations (ABS), on the emotional intensity (emotionality) associated with negative intrusive thoughts (or intrusions).

Participants needed: 150
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of LorraineUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Present symptoms of acute stress (score between 22 and 35 on the Impact Event Sc... [+7]

Be an adult protected under guardianship or curatorship; [+10]

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

Acute Effects of Stimulant Medication in College Students With ADHD

The investigators will examine the acute effects of stimulant medication on executive functioning. The rationale for the proposed study is to examine the efficacy of stimulants for college students with ADHD and help prevent stimulant misuse among college students without ADHD. The working hypothesis is that stimulants, compared to baseline and placebo conditions, will improve executive functioning for college students with ADHD but not for college students without ADHD. Improvements on executive functioning measures (e.g., CPT-IP, Spatial Span) will be examined through 2 (ADHD vs. non-ADHD) x 3 (Baseline, Placebo, Stimulant) repeated measures ANOVAs. Follow-up analyses will include paired comparisons. Expected outcomes are to confirm these hypotheses and demonstrate the need for further study of stimulants. If confirmed, the results will provide pilot data for a larger NIH grant proposal aimed at further examining the acute effects of stimulants (i.e., improved cognitive functioning with stimulants) and comparing them to the acute effects of physical exercise (i.e., improved cognitive functioning immediately after exercise). The investigators expect this outcome to have an important positive impact because it can help support stimulant medication as an effective treatment for college students with ADHD (DuPaul et al., 2012). Additionally, demonstration that stimulants do not improve executive functioning for college students without ADHD can be used to help prevent and discourage stimulant misuse and diversion on college campuses (Hartung et al., 2013).

Participants needed: 40
Trial details
Phase: Phase 2Age: 18-29Biological sex: AllType: InterventionalSponsor: University of WyomingUpdated: Jun 10, 2024Locations: 1
Eligibility criteria

Be currently enrolled either full time or part time as an undergraduate in a 2-y... [+4]

Not meeting any of the above stated inclusion criteria [+24]

Status: Recruiting

Acute Effects of Exercise in College Students With ADHD

The overall objective of this study is to examine physical exercise as an intervention for ADHD. The rationale for the proposed study is that physical exercise could serve as an effective treatment for college students with ADHD that has low costs, low risks, and ancillary health benefits and may address the limitations of existing treatments. The central hypothesis is that college students with ADHD will exhibit greater degrees of improvement in executive functioning (i.e., sustained attention, working memory) immediately following sprint interval training (SIT), relative to non-ADHD peers. This hypothesis was formulated based on preliminary studies demonstrating reduced ADHD symptoms and improved executive functioning following physical exercise. Multiple 2 (ADHD vs. control) x 2 (male vs. female) x 2 (exercise vs. none) repeated measures ANOVAs will be conducted to compare students with ADHD (n = 24) to controls (n = 24). The expected outcomes are to confirm this hypothesis and demonstrate the need for further study of physical exercise. If confirmed, the results will provide pilot data for a larger NIH grant proposal aimed at further examining the acute effects of physical exercise (i.e., improved cognitive functioning immediately following exercise) and also the chronic effects of physical exercise (i.e., improved functioning after engaging in regular exercise for an extended period). This outcome is expected to have an important positive impact because physical exercise may serve as an effective treatment for college students with ADHD that is less risky than stimulants, less time-consuming than therapy, and provides ancillary health benefits (i.e., increasing physical fitness, decreasing obesity).

Participants needed: 48
Trial details
Age: 18-29Biological sex: AllType: InterventionalSponsor: University of WyomingUpdated: Jun 10, 2024Locations: 1
Eligibility criteria

Age between 18 and 29 years. [+1]

Predominantly hyperactive/impulsive presentations of ADHD (ADHD-HI), as this pre... [+6]