Found 699 none trials
A listing of none medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
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The purpose of this study is to evaluate memory, language and cognitive difficulties in patients with ALS. ALS is a neurological disease that affects nerve cells (motor neurons) in the brain and spinal cord. This condition largely affects the muscles however there are some individuals who also experience other neurological …
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You are being asked to take part in this research study because you have Crohn’s disease and the medical treatments you have tried have not brought you to full remission (clinically and physically symptom-free).
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This study is being performed to assess how certain chronic disabilities - stroke, UE amputation, SCI, CP - differ from healthy subjects in their ability to perform ADLs. By studying the kinematics of the respective cohort of study participants as they are assesed performing common ADLS, our research team aims …
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Our objective is to compare the accuracy, costs, and cost-effectiveness of three fidelity measurement methods to assess fidelity to cognitive-behavioral therapy for youth. We will randomize 135 therapists, trained in cognitive-behavioral therapy to 3 conditions: self-report, chart stimulated recall, and behavioral rehearsal. To calculate our outcomes of interest, each condition …
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The main purpose of this research study is to assess how quitting smoking affects memory and attention.
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Are you between the ages of 18-70? Do you have an ileostomy? You may be eligible for this study!
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This project develops a SmarToyGym where sensorized, wireless toys are placed within the reach of infants to elicit body, arm/hand and leg movements. The objective is to conduct pilot testing of the SmartToyGm with atypical and typical infants. A battery of metrics will be identified to discriminate between high and …
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Up to 9 weeks, including Screening (up to 3 weeks), up to 2 weeks for Lead-in Period and residential Treatment Period receiving decreasing doses of Buprenorphine and increasing doses of either active or placebo Naltrexone, 4-5 days for VIVITROL induction and post-VIVITROL monitoring, and a 4-week outpatient follow-up period.
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The primary purpose of this study is to determine the therapeutic effectiveness of Ifetroban to improve sinus and nasal symptoms and quality of life in subjects with Aspirin Exacerbated Respiratory Disease (AERD).
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Dr. Neill Epperson and her study team at the Penn Center for Women's Behavioral Wellness are seeking women to help understand the effects of a stimulant medication on memory and attention in women who underwent surgically induced menopause.
