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Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility

Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility (SWIFT-CORE-101)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06412536
Acronym
SWIFT-CORE-101
Enrollment
10000
Registered
2024-05-14
Start date
2024-05-30
Completion date
2029-04-17
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Obesity, PreDiabetes, Diabetes Type 2, Metabolic Syndrome

Brief summary

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.

Interventions

Blood work on some participants to review eligibility for future clinical trials

Sponsors

Brooklyn Clinical Research
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants who are interested in industry-sponsored clinical research5 yearsNumber of participants who are interested in industry-sponsored clinical research in each of the following therapeutic areas: cardiovascular, obesity, and endocrine.

Secondary

MeasureTime frameDescription
Characteristics associated with patient populations interested in clinical trials5 yearsCharacteristics associated with patient populations interested in clinical trials stratified by demographics and therapeutic areas

Countries

United States

Contacts

Primary ContactAmmara Mushtaq, MD
amushtaq@brooklynclinicalresearch.com929-203-5879
Backup ContactKatherine Azer, MS
kazer@brooklynclinicalresearch.com929-332-7848

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026