We help Clinical Researchers and Patients Connect To
Take Your Clinical Trial to the Next Level!
Participating in a clinical trial is an important personal decision. The following are frequently asked questions to provide information about clinical trials.
Why do clinical trials exist?
The United States Food and Drug Administration (FDA) require that all prescription medications be evaluated for safety and efficacy before they are marketed to the public. So before a new medication can be made available, it must undergo extensive testing. Clinical trials are part of this testing process.
Why participate in a clinical trial?
Participants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.
Who can participate in a clinical trial?
All clinical trials have guidelines about who can participate; using inclusion/exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called “inclusion criteria” and those that disallow someone from participating are called “exclusion criteria”. These criteria are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions. Before joining a clinical trial, a participant must qualify for the study. Some research studies seek participants with illnesses or conditions to be studied in the clinical trial, while others need healthy participants. It is important to note that inclusion and exclusion criteria are not used to reject people personally.
What is informed consent?
Informed consent is the process of learning the key facts about a clinical trial before deciding whether or not to participate. It is also a continuing process throughout the study to provide information for participants. To help someone decide whether or not to participate, the doctors and nurses involved in the trial explain the details of the study. Then the research team provides an informed consent document that includes details about the study, such as its purpose, duration, required procedures, and key contacts. Risks and potential benefits are explained in the informed consent document. The participant then decides whether or not to sign the document. Informed consent is not a contract, and the participant may withdraw from the trial at any time.
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Central Nervous System
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We believe we’re facilitating real progress.
We believe that most people are not far from turning the corner on their mental illness – or other treatable condition. Our company was founded by people that either suffered with, or had loved ones that suffered with severe forms of depression, eating disorders and adult ADHD. We know how important it is to find a treatment that works.
Getting new medications to market is expensive and time consuming – and we both rely on AND serve the people who have found conventional medications ineffective. When you interact with our company, you do so with dignity – as we operate in a stigma-free environment. Everyone’s story is different – so we’re not concerned with why you’re in the place you’re in – we’re concerned with getting you better treatment.
Privacy is of the utmost importance. We protect your information. We assist in clinical trials, but we really transact in trust.
Terms & Conditions
Integritrial Connect is a website where patients can take mental health screenings so that may qualify them for clinical trials for medications currently under development. Integritrial advertises through our robust social community on Facebook, Twitter, Instagram, Pinterest, and more! People also find us through search engines like Google, Bing, & Yahoo. Patient traffic is filtered using geographic targeting so that only patients in a geographic radius can take screenings for trials that are currently enrolling.
Registration is not required in order to access the public areas of our Website. However visitors may, at their option, choose to take screenings in order to access certain resources and areas of our Website. We do not collect personal information from individuals who choose to browse our site without registering. We are committed to consistently improving the quality of our service, website performance, and providing more relevant content to you during your visits.