Spaulding Clinical Trials—Studies That Pay
Based in Wisconsin, Spaulding Clinical Research is a Contract Research Organization (CRO) conducting clinical trials in diverse therapeutic areas and addressing burning questions in the pharmaceutical market.
The organization carries out various types of clinical studies but specializes in Thorough QT (TQT) ones.
Renowned for their cardiac expertise, Spaulding Clinical conducts medical studies for both the U.S. government and biotech startups.
Who Can Participate in Spaulding Clinical Research Studies?
It depends on the study design. Spaulding generally looks for both healthy volunteers and people with a particular health condition.
Each study has unique eligibility criteria participants must meet, but the general requirements include:
- Health history
Can I Get Compensation for Participating in Spaulding Clinical Studies?
Yes, Spaulding’s clinical trials come with monetary compensation, but the amount varies on the study type and length.
Spaulding Clinical also has a referral program. You will get $50 for every referral that completes screening, i.e. $100 if they complete a study.
To learn what the highest-paid clinical trials in your locality are, follow the hyperlink.
What Does a Spaulding Clinical Trial Involve?
Once you have applied for a trial, you will have to go through a series of steps making up the trial cycle at Spaulding. Those are:
- Phone screening
- Health screening and assessment
You will first have a phone interview. The Recruitment personnel will inform you about the trial nature, length, and time and inquire about your health history.
Once they have determined you are a good fit, they will schedule you for a screening appointment.
Health Screening and Assessment
At this stage, you will undergo health screening onsite to ensure that your overall health condition meets the inclusion criteria for a particular clinical trial.
The initial checks include:
- Physical exam
- Vital signs
- Body Mass Index (BMI)
The research team will then review your medical and medication history as well as give you a walkthrough of the Informed Consent form and all the trial steps. You will be able to ask any questions you may have before agreeing to participate.
Once you have signed the form, additional health assessment will ensue. The research team will perform several tests, including those for:
Unless otherwise specified, your screening appointment will last 3–4 hours.
Note: To participate in screening, you have to bring a valid photo ID, such as:
- State ID
- Driver’s license
The Trial Participation
Once you have been approved to volunteer, the trial can commence.
A standard Spaulding trial requires that you stay in their facility for the duration of up to 45 days, depending on the trial protocol. Some studies may require outpatient visits, but you will know whether yours is such before the trial begins.
At Spaulding, you will only participate in a Phase I trial, and you’ll have the full support of the medical personnel.
During the trial, you will undergo a series of tests necessary to collect data about the investigated treatment, and you must follow the provided instructions.
You will be in the know about the study requirements and expectations at all times.
Note that, if you want to discontinue your participation at any stage, you are allowed to do so.
What Are Clinical Trial Phases?
Drug development is a process that can take 10–15 years to come full circle. Safety and efficacy are the two pillars of its success. After passing the lab tests, the test drug has to go through clinical trial phases.
There are four of them, each testing a different aspect of a new medical treatment and involving a larger number of subjects.
How Do I Find and Enroll in Spaulding Clinical Trials?
You can find clinical trials on the Available Studies page on the Spaulding website. Once you have found the study you’d like to volunteer in, you can apply for it:
- Via an online form
- By phone at 1-800-597-4507, Monday–Friday, 8:00 a.m.–5:00 p.m. CST
Note: Though the trials available on the Spaulding website come with compelling names (Thor or Sherlock), study descriptions do not offer much information beyond general participation requirements, such as age, sex, or BMI. If you would like to learn more about a particular study, you will have to call the Recruitment Department.
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Are Spaulding Clinical Trials Safe?
Though clinical trials involve potential risks, such as subjects experiencing side effects, they are designed to minimize the hazards.
- Good Clinical Practice (GCP)
- Federal Regulations
Who Has Access to Subjects’ Records?
Only the sponsoring company, FDA, IRB, and Spaulding Clinical have access to subjects’ records and information gathered during the trial.
How Often Can I Participate in Spaulding Clinical Studies?
Depending on study protocols and sponsor’s requirements, you may need to take a 30- to 90-day rest period upon completion of the last trial you participated in.
You will have to check your eligibility for a new trial with Spaulding’s Recruitment Department.
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