Clinical Trial studies are the most lucrative of them all. A lot of people are making 5 & 6 figure incomes just by doing Clinical Trial studies alone. Clinical Trial studies focus on preventing, diagnosing, treating and controlling symptoms of sickness and disease. Clinical Trial studies are sponsored and/or funded by a variety of organizations or individuals such as physicians, medical institutions, foundations, voluntary groups, and pharmaceutical companies. Studies can take place in a variety of locations, such as hospitals, universities, doctors' offices, or community clinics. Clinical Trials offer FREE physician attention, FREE study medications, FREE exams, FREE hospice services and compensation up to $10,000 per participated study. Clinical Trial studies are available for healthy and medically challenged individuals.
What is a Clinical Trial?
A Clinical Trial is a research study designed to answer specific questions about vaccines or new therapies or new ways of using known treatments. Clinical trials also called medical research and research studies are used to determine whether new drugs or treatments are both safe and effective, has side effects, works better than currently used treatments, or helps those who are suffering from an illness, feel better. How are subjects/panels protected?
The government has strict guidelines and safeguards to protect people who choose to participate in Clinical Trials. Every Clinical Trial in the U.S. must be approved and monitored by an Institutional Review Board (IRB) to make sure the risks are as low as possible and are worth any potential benefits. What makes up the Institutional Review Board?
An IRB is an independent committee of physicians, statisticians, community advocates and others that ensures that a Clinical Trial is ethical and the rights of study participants are protected. By federal regulation, all institutions that conduct or support biomedical research involving people must have an IRB that initially approves and periodically reviews the research.Who Are Clinical Trials Sponsored By?
Clinical Trials are sponsored by government agencies; pharmaceutical companies; individual physicians; health care institutions such as health maintenance organizations (HMOs); and organizations that develop medical devices or equipment.
Is there more than one type of Clinical Trial?
Yes, there are 5 different types of Clinical Trials.
- Treatment trials-Treatment Trials test experimental treatments, new combinations of drugs, or new approaches to surgery or radiation therapy.
- Prevention trials-Prevention Trials look for better ways to prevent disease in people who have never had the disease or to prevent a disease from returning. These approaches may include medicines, vitamins, vaccines, minerals, or lifestyle changes.
- Diagnostic trials-Diagnostic Trials are conducted to find better tests or procedures for diagnosing a particular disease or condition.
- Screening trials-Screening Trials test the best way to detect certain diseases or health conditions.
- Quality of Life trials or Supportive Care trials explore ways to improve comfort and the quality of life for individuals with chronic illnesses.
Where do Clinical Trials take place?
Clinical Trials can take place in a variety of locations, such as hospitals, universities, doctors' offices, or community clinics.
Why do people enroll in Clinical Studies?
Many people find that assisting in medical research is rewarding because they:
- receive study-related physical examinations, medical care, including blood tests, and other relevant laboratory work and follow-up care, at no cost.
- receive a FREE copy of their exam results by completing a consent form to release medical information.
- are interested in receiving new, potential therapies that are not available to the public.
- receive help with current ailments.
- gain personal satisfaction, knowing that their involvement may improve the quality of life for people who are suffering from illness.
- often get compensation up to $10,000 per study.
Will participation in a Clinical study cost me anything?
No. Study-related medical examinations, investigative medications and laboratory tests that are listed in the Clinical study plan, are provided at no cost to you as long as you are a research study participant. Therefore, medical insurance is not necessary. Do I need to have a specific medical condition in order to participate in a Clinical Trial?
Yes and No, depending on the type of study being administered. Although the majority of studies are conducted to help individuals with medical problems, many research studies call for healthy volunteers. Healthy individuals are frequently needed for all types of studies. What can I expect from a Clinical Trial?
Once you are enrolled in a Clinical Trial, you should receive a study-related physical exam, study related medication, laboratory tests, and study procedures as necessary, at no cost to you. Also, during the course of the study, medical personnel will frequently meet with you to monitor your progress. Other terms and conditions may apply.
Can you give examples of the types of medications that will be tested?
You may be simply required to test a sinus and cold medication, asthma medication if you are an asthmatic, contraceptives if you are sexual active or if you have other medical problems like diabetes, high blood pressure, high cholesterol, cancer, etc., you will likely be testing medications related to your illness. Clinical Trials are also for healthy individuals. Therefore, you may be asked to test vitamins, hair dyes, skin lotion, acne creams, toothpaste, soap, mouthwash, detergent, hair growth formulas, etc.
Are there different phases of conducting Clinical Trials?
Yes. Clinical Trials are conducted in 4 phases:
- In Phase I, researchers test experimental drugs or treatments in a small group of people (20-80) for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
- In Phase II, the experimental study drug or treatment is given to a larger group of people (100-300) to see if it is effective and to further evaluate its safety.
- In Phase III, the experimental study drug or treatment is given to large groups of people (1,000-3,000) to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the experimental drug or treatment to be used safely.
- In Phase IV, post marketing studies delineate additional information including the drug's risks, benefits, and optimal use.
How long will Each Clinical Trial Be? Will I have to spend the night at the facility?
All studies vary in structure and length of commitment. Some studies may be performed as you remain an out-patient, while others may require you to spend a single night or nights at a facility.
If I am asked to stay at a facility, what can I likely expect?
Usually Volunteers who stay at the facility enjoy the comfort of semi-private rooms, each with private restroom facilities, a television and VCR. All food is normally provided, with some meals catered by local restaurants. Recreational facilities also often include a pool table and video and reading libraries. This can be an enjoyable experience, not to mention, each study that you participate in will pay you up to $10,000. How often can I participate in Clinical Trials?
Generally speaking, upon completion of a trial (including any follow-up visits), you may be eligible to participate in another study in as little as 30 days. Some protocols require a 60 or 90-day period before allowing you to participate again. The wait time is called the ‘wash-out’ period. The ‘wash-out’ period allows the investigative medication(s) to be completely eliminated before introducing another research medication into the body.
What is a protocol?
All Clinical Trials are based on a set of rules called a protocol. A protocol describes the types of people who may participate in the trial; the schedule of tests, procedures, medications, dosages; and the length of the study. The factors that allow you to participate in a Clinical Trial are called inclusion criteria and the factors that keep you from participating are called exclusion criteria. Inclusion and exclusion criteria are not used to reject people personally. Instead, the criteria is used to identify appropriate candidates.
What questions should I ask before I agree to be in a Clinical Trial?
You have the right to ask any number of questions prior to volunteering and during the process of participation. Below is a list of questions that you may want to consider asking prior to participating in any Clinical Trial:
• Who is sponsoring the trial?
• Who has reviewed and approved it?
• Has the drug or treatment in this trial been tested before? What were the results?
• Where will the trial take place and how long will it last?
• Do I have to stay in the medical facility during the Clinical Trial?
• What kinds of tests and treatments will be given? How often?
• Will my medical records be kept confidential?
• Who will see the trial results?
• How will I know if the treatment is helping me?
• Are there any risks or side effects expected from any part of the trial?
• Are there treatment alternatives? How do they compare with what the trial offers?
• Will I still be able to see my own doctor during the trial?
• How will I be compensated and how much will I be compensated?
• If the treatment works for me, can I stay on it after the Clinical Trial is over?
• Is there any long-term follow-up care scheduled as part of the trial?
How will I know if I am selected to participate?I have a busy schedule. How long will companies wait for me to respond back to invitations and will I have enough time to complete all of the assignments that I agree to?You would have to determine this one. You are responsible for managing your own hours and setting your own schedule. However, most opportunities are flexible. Most companies will give you a time frame to complete assignments while others may require your attention right away. Just keep in mind that opportunities do not lay dormant. So, be sure to quickly respond to opportunities that you are interested in.
Do I have to accept every Clinical Trials assignment?No. You are not obligated to accept any assignment and we strongly recommend that you read all materials thoroughly before accepting any assignment.
Will Divinely Successful, Inc. issue contracts, assignments and/or compensation?No, Divinely Successful, Inc. will not issue contracts, assignments or compensation for any work, at any time. The sponsoring company who elects you for the assignment will be totally responsible for compensating you. Divinely Successful, Inc. is not a Clinical Trials Firm. Nor, do we hire Clinical Trial participants. We simply connect you to companies who hire Clinical Trial participants via our Clinical Trials Secrete Source Guide and once we connect you, it is your total responsibility to actually sign up with the companies and contact each of them for assignments. Most companies will post assignments on their website or email them to you while others will simply call you as assignments become available.
How and when do I get compensated for my assignment(s)?Most companies compensate participants via check, but there are a few who use direct deposit. During screening and when selected for an assignment, the job scheduler will explain the payment procedure they use. They will also let you know when you can expect payment. If it is not clear to you, simply ask as these companies really want you to feel comfortable working with them.
Will these companies charge me a fee to register with them?No, you will not be charged a fee to register with any of the companies in our Clinical Trials Secrete Source Guide. No legitimate company would charge you a fee to work for them. The only fee that you will have to pay is the fee to access our Clinical Trials Secrete Source Guide and the fee is not to work for us but for us providing a product and services for you.
Do I have to purchase your Clinical Trials Secrete Source Guide?Although we value your business, you are certainly under no obligation to purchase our Clinical Trials Secrete Source Guide. However, doing so could be very beneficial to you as most companies located in our Clinical Trials Secrete Source Guide are private firms who don't advertise at all. Therefore, trying to locate them on your own could be an absolute nightmare.
Will I need any special software to view the Clinical Trials Secrete Source Guide?Yes, Adobe Reader is necessary to view our pdf Clinical Trials Secrete Source Guide. If you do not have adobe reader, you may download it for free by going to www.Adobe.com.
How Can I get a listing of companies who are paying participants to participate in Clinical Trials, How do I get started and how will I receive my Guide?
Out of all the guides to purchase, we strongly suggest that you purchase our Secret Source Clinical Trial Guide as Clinical Trials pay far more than the other studies. and the opportunities are known to be lush all throughout the year. To get started simply click on the "buy" button below and make your one time payment and you will be immediately forwarded to our Thank You page where you can download Clinical Trial Secrete Source Guide. Once you download our Clinical Trials Secrete Source Guide, open it up and immediately began registering with all of the companies whom we reveal and get compensated for your participation. Get started by clicking on the "buy" button now.
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