www.yourdiabetesstudies.com – Access For AcurianHealth To Qualify For Local Research Studies

Overview Of AcurianHealth :

Acurian Health offers treatments under development and helps people to connect them to clinical research studies. The company tends to match thousands of people with research studies in all over the world.

These studies can offer you the benefits like they come with no-cost study-related medications. It can also offer you the payment for your time and the travel as well along with many other services as well.

A clinical research study is a research project done to find out if medications and treatments under development are both safe and effective. Each study is unique and conducted for different reasons. A clinical research study uses human volunteers. Participants are under strict supervision of a doctor and/or health professionals throughout the study. During the study, or trial, a patient may receive a study medication or placebo (not containing the active medication). As the trial goes on, more and more information is gathered about the treatment or device under investigation.

If you have heard of clinical trials and the ‘phases’ associated with them. There are 5 phases, which are defined by the FDA (U.S. Food and Drug Administration). Three phases are most commonly known.

Phase I studies are done during the earliest part of researching a treatment. These trials are usually small and include healthy volunteers to find out the safety of the drug.

Phase II studies gather information to find out if the drug will have an impact on a certain condition. These studies typically use larger groups of volunteers and compare the drug in different ways.

Phase III studies look further into safety and effectiveness of the drugs. These studies also use larger groups of volunteers and compare the drug in different ways.

So, if you want to know more or participate in the research, you can always check this article on Diabetes and how you can join it.

Acurian health studies may offer

• No-cost study-related care

• Access to treatments under development

• Possible compensation

Those who qualify in Acurian receive

• Payment which varies by study up to $700

• No-cost study-related care from doctors

• No-cost study medication

Check the qualification for Acurian Diabetes research

For this, visit, www.yourdiabetesstudies.com

Here, at the middle of the page, type,

• Your date of birth

• Then, click on, ‘Next’.

• In the directed page type,

• First Name *

• Last Name *

• Email Address

• Phone *

• Street address

• Apt., Floor, Building

• Country *

• Zip Code *

• City *

• State

• Then, click on, ‘Next’.

You need to follow the prompts to apply for the eligibility check.

Additional tips on Acurian research

• When you make the decision to participate in a clinical trial is a personal one. People volunteer for different reasons. Some want access to the most recent treatments under development. Some want access to specialists associated with a study. Others want to help advance science.

• Here, also, by participating you many help develop future medical treatments. Whatever the reason for your interest, be sure to do your own research ahead of time and make an informed choice about participating.

• The payment part if you participate is not for all. Many trials are able to provide payment to cover costs related to your time and travel. This varies by study and location. The study site will be able to provide payment information before you decide to participate.

• Clinical research studies are conducted throughout the U.S. and the world for many different conditions. A local doctor who treats patients outside of clinical studies may be involved with a study. Or the study location may be at a doctor’s office that only conducts clinical trials.

• Either way, before you can participate, the research site will need information from you to check if you are eligible. All information you share is kept confidential.

Generally stated, the study doctors and researchers will:

• Check your health at the beginning of the research study

• Give you specific instructions for participating

• Monitor you carefully during the study

• Stay in touch after the study is completed

• In order to help you decide if you should participate, the study doctor and researchers will first explain the research study. They will then ask you to review an ‘informed consent document.’ This document describes the clinical research study, including the study: purpose, length, procedures, possible known risks and benefits of participating, and what is expected of you if you take part. After you understand all the key facts about the clinical research study, you decide whether or not to sign the document and join the study.

• Clinical research studies are regulated, following rules set by the FDA or other health authorities. The research study will follow a protocol. This is a detailed study plan that explains what the researchers will do in the study.

• Each research study must also be approved by an institutional review board (IRB) or ethics committee (EC). IRBs and ECs are groups of people who help protect the rights and welfare of people in research studies. IRBs or ECs are usually made up of doctors, scientists, religious representatives and other medical and nonmedical people.

• Your privacy will also be protected. The research team can’t tell anyone you’re participating in a research study without your permission. All of the information collected during the study will be kept confidential. Your name won’t be listed in any reports based on the study.

• Different research studies have different risks. Some study medications can have side effects, some of which may be unknown. In some studies, some people receive active study medication, while others receive a placebo. A placebo looks like a study medication, but it has no active components. However, whether you receive the placebo or active study medication, you’ll receive the same level of study-related care.

• Your study doctor or research team should review all risks with you before you sign the informed consent document.

• You have the right to leave a research study at any time. When you want to leave, tell the doctor or research team and explain your reasons for leaving.

• After a clinical research study is finished, all of the information is collected and analyzed. The information will help determine the medication/device’s safety, effectiveness, and side effects. In the U.S., final approval is given by the FDA. Outside of the U.S., similar organizations provide approval.

• It’s important to talk to your doctor about a post-study treatment plan.

Contact info

If you want to get more information on Acurian research, you can send an email to, information@acurian.com. Send fax: (215) 323-9001. Or you can write to, Attn: Privacy Officer. by regular mail at Acurian, Inc., Attn: Privacy Officer, 2 Walnut Grove Drive, Suite 375, Horsham, PA, 19044.

Reference:
www.yourdiabetesstudies.com