Cognition

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

Condition / disease
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Status: Not yet recruiting

Lion Tracks EEG Pilot: Understand Cognitive Responses to CrossFit in Mother-Child Dyads

The purpose of this study is to examine how participating in exercise together versus separately influences brain function, cognitive performance, mood, and parent-child connection in mother-child dyads. Mothers and their children will complete two fitness class visits at a participating community fitness facility/CrossFit affiliate. During one visit, mothers and children will exercise in separate age-appropriate classes, and during the other visit they will exercise together in a shared class. Before and after each exercise session, participants will complete brief assessments of cognition, mood, and brain activity using a portable electroencephalography (EEG) device. Findings from this pilot study will help determine the feasibility of conducting community-based neuroscience research and may inform future family-centered physical activity programs designed to support brain, emotional, and social health.

Participants needed: 20
Trial details
Age: 3+Biological sex: FemaleType: InterventionalSponsor: Penn State UniversityUpdated: Jul 2, 2026
Eligibility criteria

Adult participant is a mother or female primary caregiver aged 18 years or older... [+6]

Pregnancy at the time of participation. [+11]

Status: Recruiting

Exercise and Intranasal Insulin in Type 2 Diabetes

About 6.5 million adults in the United States who are 65 or older have dementia. While the exact cause of dementia is not known, it may be due to changes in the brain. Further, risk may be higher when the brain does not respond to insulin. Indeed, brain insulin resistance has emerged as a pathologic factor affecting memory, executive function as well as systemic glucose control. Regular aerobic exercise may help reduce the risk of dementia by increased blood flow to the brain and help the brain respond better to insulin. In addition, giving insulin through a nose spray (called intranasal insulin) may also help with thinking and memory. However, it is unknown if using both exercise and intranasal insulin is best for the brain.

Participants needed: 60
Trial details
Phase: Phase 2, Phase 3Age: 55-80Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Jun 30, 2026Locations: 4
Eligibility criteria

Male or female 55-80 years old [+6]

A diagnosis of dementia [+22]

Status: Recruiting

Interventions in Mathematics and Cognitive Skills

The purpose of this study is to investigate neurocognitive mechanisms underlying response to intervention aimed at enhancing, and remediating weaknesses in, numerical skills in children, including those with mathematical learning disabilities (MLD).

Participants needed: 180
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Elementary school aged children starting from first grade (6-12 years old) [+5]

History of neurological or psychiatric disorder (i.e., schizophrenia, psychosis,... [+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: Jun 24, 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

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

Cognitive Strategies in Early Psychosis 2

The goal of this clinical trial is to learn more about decision making in psychosis spectrum disorders, like schizophrenia. Participants will be people who have had symptoms of a psychosis spectrum disorder start within the last five years. The investigators will study how two study agents change decision making in people with psychosis, by asking participants to complete some brain games on the computer before and after taking the study agents. The investigators hope to improve our understanding of psychosis to help people in the future. The main research questions are: * Does a single dose of modafinil change how people with psychosis play the brain games? * Does a single dose of d-serine change how people with psychosis play the brain games? * Does a single dose of modafinil change brain activity? * Does a single dose of d-serine change brain activity? Participants will: * Complete an interview and self-report questionnaires. * Complete safety screening activities, like a blood draw, a urine drug test, and an alcohol breathalyzer test. * Complete functional Magnetic Resonance Imaging (fMRI) scans. fMRI uses magnets to take pictures of the brain. There will be six scanning appointments in the study, with two scans each. Appointments will be about a month apart. * Take a single dose of a study agent during each scanning appointment. The study agent will be taken after the first fMRI. There are three study agents in total: modafinil, d-serine, and a placebo. Each participant will take each study agent twice during the study. * Play brain games on a computer that measure decision making, thinking, and problem solving skills

Participants needed: 24
Trial details
Phase: Phase 3Age: 18-35Biological sex: AllType: InterventionalSponsor: University of MinnesotaUpdated: May 29, 2026
Eligibility criteria

Between the ages of 18 and 35 [+7]

Major neurological disorder [+39]

Status: Recruiting

Flumazenil for Benzodiazepine Reversal in Electroconvulsive Therapy

The goal of this study is to investigate whether administering flumazenil to reverse the effects of benzodiazepines and/or zopiclone during electroconvulsive therapy (ECT) can help reduce cognitive side effects without diminishing treatment effectiveness in hospitalized patients with depression. The investigators hypothesize that blockade of the GABA receptor with flumazenil will reduce cognitive side effects through improved seizures and a reduced need for electrical charge escalation during the ECT series. Cognitive side effects will be measured by the total score on the Screening for Cognitive Impairment in Psychiatry (SCIP) (primary outcome) at follow-up after completion of the ECT series. Furthermore, it is expected that the flumazenil strategy will reduce pre-treatment anxiety and improve patient satisfaction (secondary outcomes). In addition, flumazenil strategy is hypothesized to have beneficial effects on subjective cognitive complaints, autobiographical memory, and executive functioning (secondary outcomes). Finally, the flumazenil strategy is expected to be associated with more favorable structural and functional changes in executive functioning and memory-related brain networks after completion of the ECT series, which may, in turn, be linked to better overall cognition and autobiographical memory (secondary outcome measures). For exploratory purposes, the study will also examine longitudinal changes in depressive symptoms and cognitive outcomes from baseline to follow-up (tertiary outcomes). Investigators will compare two different pre-ECT benzodiazepine management strategies: 1. Flumazenil strategy (experimental): continued benzodiazepine and/or zopiclone use up until the time of the ECT session, followed by administration of flumazenil immediately prior to ECT 2. Benzodiazepine withholding strategy (treatment as usual): discontinuation of benzodiazepines and/or zopiclone prior to the ECT in accordance with standard clinical practice

Participants needed: 145
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Anders JørgensenUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Current depressive episode (unipolar or bipolar), corresponding to ICD-10 codes... [+3]

Involuntary treatment with ECT [+6]

Status: Not yet recruiting

Human Neural Correlates of Multi-Timescale Inference

Adult epilepsy patients who are undergoing intracranial monitoring will participate in a simple behavioral task during the clinical recording period.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of Colorado, BoulderUpdated: May 26, 2026Locations: 1
Eligibility criteria

Epilepsy patients undergoing intracranial electrode monitoring for uncontrolled... [+2]

seizure activity during task recording [+2]

Status: Not yet recruiting

The Effects of High-Intensity Interval Training on Gait, Balance, and Cognitive Functions in Individuals With Multiple Sclerosis

This study aims to comparatively investigate the effects of low-volume High-Intensity Interval Training (HIIT) versus Moderate-Intensity Continuous Training (MICT) on gait, balance, cognitive functions, and neurovascular biomarkers (BDNF, VEGF) in individuals with Multiple Sclerosis (MS). This randomized controlled trial will be conducted at Hacettepe University, Faculty of Physical Therapy and Rehabilitation.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hacettepe UniversityUpdated: May 20, 2026Locations: 1
Eligibility criteria

Diagnosed with Multiple Sclerosis by a neurologist (Hacettepe University Hospita... [+5]

Status: Recruiting

Acute Impact of Whey Protein-enriched Milk Fat Globule Membrane Supplementation on Postprandial Markers of Heart and Brain Health

In a single-blind, randomised, placebo-controlled crossover manner, this study aims to assess the impact of a high-fat mixed meal containing a whey protein (WP)-enriched milk fat globule membrane (MFGM) powdered ingredient on markers of heart and brain health in the fed state among middle-to-older-aged, postmenopausal women living with overweight and at moderate risk for cardiovascular disease. Participants will attend two \~8 hour study visits, where they will consume a high-fat meal containing a WP-enriched MFGM powdered ingredient or a placebo WP-based powdered ingredient. Each visit will involve anthropometric measurements and periodic assessments of heart health, including blood pressure and blood vessel stiffness measurements, blood sample collections, as well as computer-based tests measuring mood and cognition (brain function) over a 6-hour postprandial period.

Participants needed: 16
Trial details
Age: 50-75Biological sex: FemaleType: InterventionalSponsor: Loughborough UniversityUpdated: May 20, 2026Locations: 1
Eligibility criteria

Apparently healthy postmenopausal women (not menstruating for 12 or more months) [+7]

Smoking (including vaping) [+14]

Status: Not yet recruiting

Retrospective Analysis of CPET and Cognitive Tests of Healthy Individuals, Treated With 60 Treatment of HBOT

This retrospective observational study evaluates physiological and cognitive changes following a series of 60 hyperbaric oxygen therapy (HBOT) sessions in healthy individuals. Participants underwent treatment five days per week, each session included 90 minutes exposure to 100% oxygen at 2ATA with a five-minute air break every 20 minutes. Pre- and post-treatment data include cardiopulmonary exercise testing (CPET) and standardized cognitive assessments. The study aims to characterize associations between changes in cardiorespiratory fitness and cognitive performance following repeated HBOT exposure in a real-world clinical cohort

Participants needed: 1,000
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Assaf-Harofeh Medical CenterUpdated: May 19, 2026
Eligibility criteria

Adults aged 18-65 years [+3]

Inability to complete a maximal CPET test, pre and post HBOT or Missing pre- or... [+2]

Status: Not yet recruiting

Development of a Chatbot-supported Personalized Exercise Program for Older Adults and Evaluation of Its Effects on Cognitive Functions

The purpose of this study is to develop an artificial intelligence-based chatbot application to support exercise behavior in individuals aged 60 and over who do not regularly exercise, and to evaluate its effectiveness. In addition, the study aims to examine the effects of changes in exercise habits on the cognitive (mental) functions of older adults. In this study, the impact of a chatbot-supported personalized exercise program on cognitive functions in older individuals will be evaluated. A total of 90 participants is planned for inclusion in this study. If you agree to participate in this study, depending on the group you are assigned to, you may receive: * An artificial intelligence-based chatbot program, along with educational materials about the importance of exercise, or * Only educational materials (brochures) prepared by the researchers about the importance of exercise. At the beginning of the study, you will be asked to complete a data collection form. The same form will also be administered at week 12 and week 24. This form will include: * Basic information such as your age and gender, * Questions about your exercise habits, * A brief test to assess your cognitive (mental) functions, * Questions evaluating your level of physical activity. The study duration is 24 weeks, including 12 weeks of intervention and 12 weeks of follow-up.

Participants needed: 90
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Dokuz Eylul UniversityUpdated: May 19, 2026Locations: 1
Eligibility criteria

Aged 65 years and older [+4]

Moderate to severe dementia [+4]

Status: Not yet recruiting

Assessing the Effects of Cool Roofs on Indoor Environments and Health in Tavua, Fiji

Ambient air temperatures in Fiji are increasing due to climate change. Solutions are needed to build heat resilience in communities and adapt. Sunlight-reflecting cool roof coatings may passively reduce indoor temperatures and energy use to protect home occupants from extreme heat. Occupants living in poor housing conditions in Fiji are susceptible to increased heat exposure. Heat exposure can instigate and worsen numerous physical, mental and social health conditions. The worst adverse health effects are experienced in communities that are least able to adapt to heat exposure. By reducing indoor temperatures, cool roof use can promote physical, mental and social wellbeing in household occupants. The long-term research goal of the investigators is to identify viable passive housing adaptation technologies with proven health benefits to reduce the burden of heat stress in communities affected by heat in Fiji. To meet this goal, the investigators will conduct a cluster-randomized controlled trial to establish the effects of cool roof use on health, indoor environment and economic outcomes in Tavua, Fiji.

Participants needed: 800
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Aditi BunkerUpdated: May 18, 2026Locations: 1
Eligibility criteria

Permanent household resident.

Roof damage, inaccessible or instability of roof adversely affecting cool roof c... [+1]

Status: Recruiting

iFD-SuRvivE funCtiONal effiCacy and bIologicaL corrElates (RECONCILE Study)

The goal of this clinical trial is to assess the effectiveness of an original intervention 'Functional Recovery in Depression and Suicide Risk Prevention Based on Emotion Regulation and Values: A Group Program' (from the original Spanish version: Programa Grupal De Recuperación Funcional En Depresión Y Prevención De Riesgo Suicida Basado En Regulación Emocional Y Valores) in depressed patients who have recently attempted suicide by improving their psychosocial functioning and therefore enhancing their ability to perform activities of daily living. As secondary objectives, the effectiveness of the intervention will be evaluated by determining cognitive performance (particularly decision-making, inhibition, and attention), quality of life, clinical status, and their relationship with neuroimaging correlates. Main target neuroimaging areas include the orbitofrontal cortex and dorsal prefrontal cortex.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Iria GrandeUpdated: May 12, 2026Locations: 4
Eligibility criteria

Age over 18 years old [+3]

Intelligence quotient below 70 and impaired functioning [+4]

Status: Not yet recruiting

The Impact of Brief Behavioral Treatment for Insomnia Versus Brief Mindfulness Treatment on Cognition and Sleep Health in Adults (Age 50+) With HIV

The goal of this clinical trial is to examine the effects of a telephone-delivered Brief Behavioral Treatment Insomnia (BBTI) versus a Brief Mindfulness Treatment (BMT) on cognitive and sleep outcomes in older adults with HIV. The main questions it aims to answer are: What are the effects of BBTI vs BMT on self-reported and observed sleep outcomes in older adults with HIV and insomnia up to 1-year post-intervention? What are the effects of BBTI vs BMT on self-reported and observed cognitive comes in older adults with HIV and insomnia up to 1-year post-intervention? What is the association between Alzheimer's Disease biomarkers and sleep and cognitive outcomes in older adults with HIV receiving BBTI vs BMT? Participants will: * Complete 4 weeks of telephone-delivered BBTI or BMT * Attend baseline, post-intervention, and 1-year post in-person visits for sleep and cognitive assessments * Have blood collected at all three time points

Participants needed: 214
Trial details
Age: 50-99Biological sex: AllType: InterventionalSponsor: University of Alabama, TuscaloosaUpdated: May 8, 2026Locations: 2
Eligibility criteria

must be age 50 or older [+2]

unable to speak English [+12]

Status: Not yet recruiting

DEVELOPMENT AND PSYCHOMETRIC EVALUATION OF THE NEUROCOGNITIVE UPPER EXTREMITY TESTS: A RELIABILITY AND VALIDITY STUDY

The goal of this observational study is to develop an upper extremity neurocognitive performance test battery, determine its reliability and validity, and investigate the effect of neurocognitive load on test performance in athletes and healthy volunteers aged 18-40. The main questions it aims to answer are: Are the developed upper extremity neurocognitive tests reliable and valid tool for assessment? Does the addition of neurocognitive load significantly affect upper extremity physical performance scores? Are the neurocognitive performance test results related to shoulder rotator cuff muscle strength, rate of force development, and shoulder function? Researchers will compare the neurocognitive performance of athletes to healthy non-athlete individuals to see if the test battery can effectively differentiate between these two groups (discriminative validity). Participants will: Complete demographic forms and questionnaires regarding activity level and shoulder function. Undergo shoulder range of motion and isometric strength/rate of force development assessments. Perform a battery of 4 neurocognitive tests integrated with a light-based reaction system. Perform the same functional tests without neurocognitive load to serve as a baseline for comparison. (Athletes only) Attend additional sessions to evaluate the feasibility of the tests and to assess test-retest reliability with a one-week interval.

Participants needed: 30
Trial details
Age: 18-40Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: May 12, 2026Locations: 1Duration: 1 Week
Eligibility criteria

Individuals between the ages of 18 and 40 [+11]

Presence of symptomatic upper extremity pathology [+5]

Status: Recruiting

GUTLINK4KIDS Intervention

This study aims to investigate the chronic effects of prebiotic consumption on cognitive, behavioural and gut microbiome outcomes in children aged 3-5 years.

Participants needed: 106
Trial details
Age: 3-5Biological sex: AllType: InterventionalSponsor: University of ReadingUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Parents (18 years and over) of generally healthy children aged 3-5-years-old (36...

Children with a significant acute or chronic co-existing illness (including infl... [+2]

Status: Not yet recruiting

Intensive Music Therapy on Cognitive Function in Subacute Stroke Rehabilitation in Malaysia

The purpose of this study is to explore whether intensive music therapy can help improve cognitive functions like memory, attention, and decision-making skills in stroke patients who are undergoing rehabilitation. This is a feasibility study, meaning it's also designed to see how practical it is to include music therapy as part of stroke rehabilitation. The investigators want to learn how well patients can participate in and stick with this type of therapy, and whether it fits well with other treatments that stroke patients usually receive. By understanding this, the investigators can assess the resources, staff training, and planning needed for music therapy to be part of stroke recovery in the future. The study will also help the investigators estimate the effects of music therapy, which will be used to design a larger, more detailed study in the future.

Participants needed: 36
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: University of MalayaUpdated: May 1, 2026
Eligibility criteria

Diagnosed with ischemic or haemorrhagic stroke confirmed by CT scan [+5]

Severe aphasia [+4]

Status: Recruiting

ETASCAN Project: ETAS Project 2

This study aims to investigate the chronic effects of ETAS® on cognitive, affective and neural outcomes in healthy adults aged 60-80 years with mild to moderate subjective cognitive complaints.

Participants needed: 60
Trial details
Age: 60-80Biological sex: AllType: InterventionalSponsor: University of ReadingUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

Aging between 60-80 years old [+3]

Smoking [+25]

Status: Not yet recruiting

Effects of Cognitive Dual-Task on Gait in Parkinson's Disease

The aim of this study is to evaluate gait in individuals diagnosed with PD under tasks involving different cognitive domains, to compare the results with those of age and sex-matched healthy individuals, and to determine which cognitive function has the greatest impact on gait in PD.

Participants needed: 30
Trial details
Age: 40-80Biological sex: AllType: ObservationalSponsor: Gazi UniversityUpdated: Apr 20, 2026Locations: 1Duration: 2 Days
Eligibility criteria

A clinical diagnosis of Parkinson's Disease confirmed by a neurologist according... [+5]

Presence of any neurological disorder other than Parkinson's Disease [+9]

Status: Recruiting

Magnesium and Cognition After Stroke

Cognitive impairments such as memory impairments, word-finding difficulties, compromised orientation and perception are often observed in stroke patients. Low serum-mg-concentrations are associated with cognitive impairments in ischemic stroke patients one month after stroke onset. It is not clear, if cognitive impairments after stroke is caused by the mg-deficiency or by the stroke itself. Until now, no studies investigating the relationship between mg-concentration, stroke severity and cognition during treatment course are available. Thus, this study aimed to investigate the relationship between mg-concentration and cognition of stroke patients.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: BDH-Klinik Hessisch OldendorfUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

ischemic/hemmorhagic stroke [+1]

pre-existing dementia or cognitive impairment before stroke onset [+4]

Status: Recruiting

Do Antipsychotics Block Insulin Action in the Brain: is it a Class Effect?

This study aimed at helping researchers understand how a medication called haloperidol can affect insulin action in the brain. Insulin is a hormone in the body that controls sugar levels in part by lowering the amount of glucose produced by the liver. After eating a meal, insulin levels go up in both the blood and the brain. Insulin in the brain has also been shown to affect the way the brain works and processes information (also known as "cognition"). Haloperidol, is an antipsychotic medication used to treat a variety of disorders such as schizophrenia spectrum disorders, bipolar disorder, and major depressive disorder, but long-term use can have metabolic side effects, like weight gain, type 2 diabetes, and cardiovascular disease. The purpose of this study is to investigate how antipsychotic medications, such as haloperidol, which carries the risk of metabolic changes, might interrupt the effect of insulin action in the brain. This will help researchers learn how to potentially reduce metabolic risk for people who take these kinds of medications in the future.

Participants needed: 35
Trial details
Phase: Phase 4Age: 18-35Biological sex: AllType: InterventionalSponsor: Centre for Addiction and Mental HealthUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Must be deemed to have the capacity to provide informed consent [+5]

History of psychiatric illness, including any substance use (screened using the... [+16]

Status: Recruiting

Effects of Breathing Exercises on Cognition in Older Adults

The goal of this interventional clinical trial is to investigate the effects of breathing exercises added to balance training on cognitive function in individuals aged 65 years and older. The main questions it aims to answer are: Do breathing exercises affect cognition? Do different breathing exercises affect cognition in different ways? Researchers will administer two different breathing protocols and evaluate cognition before and after each protocol. Participants will take part in an 8-week program consisting of sessions that include 30 minutes of balance-based exercises and 15 minutes of breathing exercises. Sessions will be held twice weekly under the supervision of a physical therapist.

Participants needed: 40
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Istanbul University - CerrahpasaUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Adults aged 65 years and older [+3]

Underwent surgery within the last 6 months [+2]

Status: Recruiting

Modeling the Effects of Chronic Marijuana Use on Neuroinflammation and HIV-related Neuronal Injury

This study applies a hypothesis-driven approach to examine the effects of chronic marijuana use on HIV-associated inflammation and its subsequent impacts on central nervous system function, with the goal of identifying the mechanisms through which cannabinoids modulate neurological disorders and other comorbidities in persons with HIV.

Participants needed: 220
Trial details
Age: 25-59Biological sex: AllType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

verified HIV status [+6]

Lifetime abuse for any illicit drug other than marijuana [+7]

Status: Not yet recruiting

The Effect of Remotely Delivered Pilates on Physical , and Psychological Outcomes in Individuals With Multiple Sclerosis

Objectives Objective 1: To determine the effects of a 16-week remotely delivered Pilates intervention on walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS. Objective 2: To examine the impact of a 16-week remotely delivered Pilates intervention on depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS. Aim Aim 1: To assess whether the 16-week remotely delivered Pilates intervention significantly improves walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS Aim 2: To investigate whether the 16-week remotely delivered Pilates intervention significantly improves depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS. Hypothesis Hypothesis 1: The 16-week remotely delivered Pilates intervention will significantly improve walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS. Hypothesis 2: Participants receiving the 16-week remotely delivered Pilates intervention will demonstrate significantly greater improvements in depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Illinois at ChicagoUpdated: Mar 31, 2026
Eligibility criteria

Age 18 years or older [+10]

Pregnant [+1]