CClinicalTrials.gg
RecruitingNCT06492187Updated Jul 9, 2024

Triage Survey for Infectious Disease Eligibility

An observational study in Vaccination; Infection, HIV-1-infection and Infectious Disease, sponsored by Brooklyn Clinical Research. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-09.

Sponsored by Brooklyn Clinical Research · Observational

From the registry’s dates

  • Started Jun 2024; still recruiting 2 years 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
10,000
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Vaccination; Infection
  • HIV-1-infection
  • Infectious Disease
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's planned enrollment of 10,000 is above the median of 240 across 2,136 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Brooklyn Clinical Research is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

In total of the program, we anticipate 10,000 participants of any sex, gender, age 18+, who have expressed interest in participating in a clinical trial of an investigational product such as device or drug, for indications in infectious diseases related therapeutic areas will be screened for clinical appropriateness for a study trial.

Inclusion criteria

    1. Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
  1. Participant is at least 18 years old.

Exclusion criteria

Exclusion Criteria:

  1. Participants are 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 or makes them unsuitable for the study for another reason.
  3. Current or recent moderate or severe substance use disorder impacting their ability to follow study related procedures.
  4. Reported history of coagulopathy or bleeding disorder considered a contraindication to phlebotomy.
  5. Any condition that in the investigator's opinion makes a participant unsuitable for the clinical trial study.
  6. 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.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
10,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Number of participants interested in clinical research

    Number of participants for whom an industry-sponsored clinical research clinical research is clinically appropriate for HIV, vaccines, and other infectious diseases

    Time frame: 5 years

Secondary outcomes

  1. Clinical Trial Enrollment

    Proportion of the clinical trial seeking population who enroll in industry-sponsored studies in infectious diseases therapeutic area.

    Time frame: 5 years

Other outcomes

  1. Disqualifying conditions

    Prevalence of disqualifying comorbid conditions that prevent screening or enrollment in industry-sponsored clinical research for HIV, vaccines, and other infectious diseases.

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06492187
Lead sponsor
Brooklyn Clinical Research
Responsible party
Sponsor
First posted
Jul 9, 2024
Start date
Jun 28, 2024
Primary completion
Jan 28, 2029 (estimated)
Completion
Jan 28, 2029 (estimated)
Last update
Jul 9, 2024

Study contacts

Ammara Mushtaq, MD
Contact
amushtaq@brooklynclinicalresearch.com
9292035879
Katherine Azer, MS
Contact
kazer@brooklynclinicalresearch.com
9293327848

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion