Paid Clinical Trials in Baltimore, MD
Here are the 6 most popular medical studies in paid studies baltimore
Behavioural Intervention
Medically Tailored Meals for Heart Failure
Recruiting0 awards
Philadelphia, Pennsylvania
This protocol is designed to compare the effectiveness of two dietary intervention doses for patients with heart failure (HF) and malnutrition risk or malnutrition at hospital discharge. This random order crossover design will provide evidence as to whether the provision of dinner meals alone versus all 3 daily meals to patients' homes is more effective at improving malnutrition risk score, and secondarily unplanned emergency department visits and readmissions.
Healthy Volunteers, not taking Tenofovir (TFV) based PrEP for Aging
Recruiting1 award10 criteria
Baltimore, Maryland
The goal of this clinical study is to learn about the effect of aging on certain enzymes, or proteins, in the blood and colon. The study involves collection of blood and colon tissue biopsies using a flexible sigmoidoscope or colonoscope. This study is also investigating how medications tenofovir and emtricitabine interact with certain enzymes. The investigators will compare the difference in enzyme activity between people taking tenofovir and emtricitabine, to those who are not taking tenofovir and emtricitabine.
Behavioral Intervention
REDES +1 More for COVID-19
Recruiting1 award9 criteria
Baltimore, Maryland
This trial aims to find the best way to get more Latino adults and their networks vaccinated against COVID-19. It will compare the effectiveness of motivational interviewing with just giving information about the vaccine.
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Clinical Trials With No Placebo
View 86 medical studies that do not have a placebo group.
Behavioural Intervention
Time Restricted Eating for Intermittent Fasting
Recruiting1 award5 criteria
Newark, Delaware
This trial will study how limiting food/drinks to 10h/day affects diet, eating habits, and body composition in women aged 20-29. Participants will record diet for 1wk before and after the 4wk trial.
Healthy controls for Opioid Use Disorder
Recruiting1 award4 criteria
Philadelphia, Pennsylvania
The 5-year K01 Mentored Research Scientist proposal will employ brain, neurocognitive, and computational tools (e.g., machine learning) to understand the impact of opioid-use disorder (OUD) and common co-occurring issues on executive function and clinical outcomes. There have been record numbers of fatal and non-fatal overdoses (ODs) associated with opioids (and other drugs) in the past 12-months. Improving classification and predictive capabilities to enhance treatment and prevent relapse is of the upmost importance. Deficits in neurocognition often are associated with poor treatment outcomes (e.g., more drug use, medication non-adherence), yet co-occurring issues associated with OUD (e.g., depression, anxiety, physical/sexual abuse, neglect) make it difficult to parse which contributing factors lead to worse executive function (EF) and poorer treatment outcomes. Novel brain, neurocognitive, and computational tools are needed to help determine these differences, in order to lay the foundation for better treatments. This need has shaped both the training plan and the associated research project in a 5-year K01 Mentored Research Scientist proposal, building on Dr. Regier's prior preclinical and clinical addiction neuroscience experience (focused mostly on cocaine-use disorders, cue-reactivity, subcortical networks, prior adversity, and univariate imaging techniques).
Immobilization Group for Proximal Humeral Fractures
Recruiting1 award3 criteria
Camden, New Jersey
The purpose of this study is to evaluate compare postoperative range of motion in patients who are given a sling for comfort only and allowed to start early active range of motion compared to patients who are placed in a sling for 4 weeks with passive range of motion only. Once enrolled, the patients will be randomized through computer randomization then placed in paper packets into either the immobilization group or the early range of motion group.
Arm 1 (Introductory Message A + Tobacco Use Message A + Incentive) for Lung Cancer
Recruiting1 award2 criteria
Philadelphia, Pennsylvania
This trial tests different messages to increase response rates to a survey that estimates eligibility for lung cancer screening. This helps improve future interventions to increase screening.
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Frequently Asked Questions
Do I need insurance to participate in a trial?
Almost all clinical trials will cover the cost of the 'trial drug' — so no insurance is required for this. For trials where this trial drug is given alongside an already-approved medication, there may be a cost (which your insurance would normally cover).
Is there any support for travel costs?
Many of the teams running clinical trials will cover the cost of transportation to-and-from their care center.
Will I know what medication I am taking?
This depends on the specific study. If you're worried about receiving a placebo, you can actively filter out these trials using our search.
How long do clinical trials last?
Some trials will only require a single visit, while others will continue until your disease returns. It's fairly common for a trial to last somewhere between 1 and 6 months.
Do you verify all the trials on your website?
All of the trials listed on Power have been formally registered with the US Food and Drug Administration. Beyond this, some trials on Power have been formally 'verified' if the team behind the trial has completed an additional level of verification with our team.
How quickly will I hear back from a clinical trial?
Sadly, this response time can take anywhere from 6 hours to 2 weeks. We're working hard to speed up how quickly you hear back — in general, verified trials respond to patients within a few days.