TRIAL PARTICIPATION

Northwest Clinical Research Center is looking for males, ages 18-45, to participate in a clinical research study evaluating a new medication that will target the hormones responsible for neural concentration and social skills and its association with Adult Autism Spectrum Disorder. This trial requires that the patient either lives with or is in regular contact with a caregiver.

Study participants will receive the following at NO COST:
      Medical Evaluation
      Medical Care
      Study Medication

For more information about clinical trials or to talk to someone in our office, please call 1-877-453-0404 or simply complete the questionnaire.

FREQUENTLY ASKED QUESTIONS ABOUT CLINICAL TRIALS
Why do clinical trials exist?
The United States Food and Drug Administration (FDA) requires 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.

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. Instead, the criteria are used to identify appropriate participants and keep them safe. The criteria help ensure that researchers will be able to answer the questions they plan to study.

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.

Does it cost anything to participate in the study?
There is no monetary cost to you to participate in this study, nor do you have to pay for the study drug, visits, or procedures that are a part of the clinical trial.