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Cognition clinical trials

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NCT ID: NCT05460624 Withdrawn - Cognition Clinical Trials

Daily Egg Consumption and Cognitive Function in Older Adults

Start date: February 10, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effects of provisioning twelve eggs weekly, incorporated into breakfast meals, on composite scores of executive functioning and memory using the CNSVS computerized test platform in older adults in a randomized study.

NCT ID: NCT04652856 Withdrawn - Cognition Clinical Trials

Neurocognitive Basis of Attention and Eye Movement Guidance in the Real World Scenes

Start date: May 2022
Phase: N/A
Study type: Interventional

The objective of this study is to determine the effects of electrical brain stimulation (EBS) on visual search in natural scenes in humans.

NCT ID: NCT04540523 Withdrawn - Physical Activity Clinical Trials

Home-Based Exergaming Intervention

Start date: September 8, 2020
Phase: N/A
Study type: Interventional

This study will employ a 3-arm randomized clinical trial to determine the effects of a 6-month home-based exergaming intervention on preschoolers' physical activity, health-related fitness, cognition, and screen time, across time, at 3, 6 and 12 months, and as an exploratory outcome, will explore the moderating effects of parent involvement and physical home environment on the intervention role of exergaming across time. Briefly, a total of 330 child-parent dyads from the Twin Cities area in Minnesota will be individually randomly assigned to: 1) an exergaming intervention group (30 min. per session, 5 sessions exergaming play per week for a 6-month period); 2) a traditional PA group (phone consultations and workshops for parents to offer 5 times 30 min. PA at home for 6 months); and 3) an attention control group (continue with usual activities at home with emailed PA tips).

NCT ID: NCT03629106 Withdrawn - Bipolar Disorder Clinical Trials

Effects of Cannabis Abstinence on Symptomology and Cognition in Bipolar Disorder

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to assess the changes in symptoms and cognition that occur after a 28-day abstinence period in patients with comorbid Cannabis Use Disorder (CUD) and Bipolar (Type I or II) disorder. Stabilized bipolar patients (N=52) with CUD will be randomly assigned to one of two groups: 1) A contingent reinforcement (CR) group (n=26); 2) a non-contingent reinforcement (NCR) group (n=26). The study will include a total of 8 visits to the CAMH Russell site (screening, training, baselines, week 1-4, follow-up). Participants should be between the ages of 18-60, meet criteria for CUD (moderate to severe), meet criteria for Bipolar Disorder, be on a stable dose of mood stabilizing medication(s), and be non-treatment seeking cannabis user. The visits will take up a total of approximately 22.5 hours with compensation for time provided for both groups. These visits will involve multiple clinical, substance use, and cognitive assessments. Abstinence will be maintained by weekly behavioural coaching sessions and contingency reinforcement for the CR group.

NCT ID: NCT03224559 Withdrawn - Cognition Clinical Trials

Applying Neuromodulation to Accelerate Training Effects

ANeMATE
Start date: September 1, 2019
Phase:
Study type: Observational

This study seeks to understand at how noninvasive electrical brain stimulation might change how people perform on on tasks requiring concentration and thinking skills.

NCT ID: NCT02246075 Withdrawn - Dementia Clinical Trials

Study of the Safety of Two Doses of Investigational Study Drug EVP-6124 in Subjects With Alzheimer's Disease Currently Receiving Memantine

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of 2 fixed doses of EVP-6124 hydrochloride (HCl) compared to placebo for 24 weeks in subjects with mild to moderate Alzheimer's disease who are concurrently receiving stable treatment with memantine and currently receiving stable treatment or previously treated with an acetylcholinesterase inhibitor.

NCT ID: NCT00534898 Withdrawn - Schizophrenia Clinical Trials

Bexarotene and Fenretinide as Addition to Antipsychotic Treatment in Schizophrenia Patients

Start date: n/a
Phase: Phase 3
Study type: Interventional

Background: In this proposed study, we aim to investigate safety and efficacy of two synthetic retinoids - bexarotene (Targretin; LGD1069; 4-[1-{5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl} ethenyl] benzoic acid) and fenretinide (Dihydroceramide N-(4-Hydroxyphenyl retinamide) on severity of psychopathology and cognitive impairment in schizophrenia patients in an double-blind, placebo-controlled study. The rationale behind add-on these medications to ongoing antipsychotic treatment in schizophrenia patients is based on both the retinoid dysregulation hypothesis: the growth factors deficiency and synaptic destabilization hypothesis of schizophrenia. Furthermore, in our preliminary open clinical trial, we found that a low dose of bexarotene (Targretin, 75 mg/day) was safe and led to significant improvement on total PANSS scores, general psychopathology, on the positive and the dysphoric mood factor scores. The aim of the present study was to provide further insight into the safety and efficacy of bexarotene in comparison to fenretinide (a medication with smaller potential of adverse effects) and placebo in patients suffered from schizophrenia.