Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
10,000 (estimated)
Sponsor
Brooklyn Clinical Research · Research network
Who this trial is looking for
This trial is looking for adults who might qualify for clinical trials related to diabetes, heart disease, and obesity. Participants will answer questions about their health and may undergo some health checks with a doctor.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I have signed the consent form before any study procedures.
You may not be able to join if
I am pregnant, breastfeeding, or planning to become pregnant.
I have a significant illness that may affect my safety or study results.
I have had a moderate or severe substance use disorder in the last 90 days.
I have any condition that makes me unsuitable for the study.
I am currently employed by Swift Clinical Research Group or its subsidiaries, or I have a first-degree relative who is.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
SWIFT-CORE-101 is a single site survey study designed to assess potential participants' eligibility to screen for industry-sponsored clinical trials. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical history, comorbidities, and current symptoms. Site staff may collect vital signs, urine drug screens, blood draws, and urine pre…
SWIFT-CORE-101 is a single site survey study designed to assess potential participants' eligibility to screen for industry-sponsored clinical trials. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical history, comorbidities, and current symptoms. Site staff may collect vital signs, urine drug screens, blood draws, and urine pregnancy tests. A doctor will review medical history with the participant to determine study suitability via clinical interview. The doctor may reach out to the patient's current treating physicians and pharmacies to determine eligibility for clinical trials.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
1. Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
2. Participant is at least 18 years old.
Exclusion Criteria:
1. Participant is pregnant, breast-feeding, or planning to become pregnant.
2. History of a cl…
Inclusion Criteria:
1. Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
2. Participant is at least 18 years old.
Exclusion Criteria:
1. Participant is pregnant, breast-feeding, or planning to become pregnant.
2. History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results.
3. Moderate or severe substance use disorder within 90 days prior to screen
4. Any condition that in the investigator's opinion makes a participant unsuitable for the study.
5. Currently employed by Swift Clinical Research Group, Inc. or any of its subsidiaries, including Brooklyn Clinical Research, or a first-degree relative of an employee.
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