Actively Recruiting
Triage Survey for Infectious Disease Eligibility
Led by Brooklyn Clinical Research · Updated on 2024-07-09
10000
Participants Needed
1
Research Sites
239 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
SWIFT-ID-101 is a single site survey study designed to assess potential participants' eligibility to screen for industry-sponsored clinical trials for diagnosis, treatment, or prevention of infectious diseases such as in the areas of HIV, vaccines, and other infectious-diseases areas. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical/surgical history, physical examination, comorbidities, and any current symptoms. Informed consent will be done electronically (preferable) or on paper. Informed consent may be done in-person or remotely, depending on patient preference. Information related to HIV, hepatitis B and C, other infectious diseases, or substance use disorder will also be obtained if applicable. Site staff may collect vital signs, fingerpick testing, urine drug screens, blood draws, EKG, and pregnancy tests. Some testing may be recommended in a fasting condition. A doctor will review medical history and results of the above evaluations with the participant to determine study suitability via clinical interview. The doctor may reach out to the patient's current treating physicians, other providers, and pharmacies to determine eligibility for clinical trials. A follow-up phone call may be needed to discuss testing results and/or trial eligibility. If a participant is deemed eligible for future trials and if the participant remains interested, counseling on contraception requirements for trials will be discussed.
CONDITIONS
Official Title
Triage Survey for Infectious Disease Eligibility
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant or legally authorized representative has signed an informed consent form before any study procedures.
- Participant is at least 18 years old.
You will not qualify if you...
- Participants who are pregnant, breastfeeding, or planning to become pregnant.
- History of a serious illness that may affect participant safety or study analysis.
- Current or recent moderate or severe substance use disorder impacting ability to follow study procedures.
- History of bleeding or clotting disorders contraindicating blood draws.
- Any condition making the participant unsuitable for the clinical trial as judged by the investigator.
- Employment by Swift Clinical Research Group or relatives who are employees.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Brooklyn Clinical Research
Brooklyn, New York, United States, 11226
Actively Recruiting
Research Team
A
Ammara Mushtaq, MD
CONTACT
K
Katherine Azer, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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