Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Blood work.
- Who it may be relevant to
- Registry conditions: Cardiovascular Diseases, Obesity, PreDiabetes, Diabetes Type 2. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility (SWIFT-CORE-101)
Overview
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
- Other Blood work
Blood work on some participants to review eligibility for future clinical trials
Primary outcome measures
- Number of participants who are interested in industry-sponsored clinical research [Time frame: 5 years]
Secondary outcome measures (1)
- Characteristics associated with patient populations interested in clinical trials [Time frame: 5 years]
Eligibility criteria
Inclusion criteria
- Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
- Participant is at least 18 years old.
Exclusion criteria
- Participant is pregnant, breast-feeding, or planning to become pregnant.
- History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results.
- Moderate or severe substance use disorder within 90 days prior to screen
- Any condition that in the investigator's opinion makes a participant unsuitable for the study.
- 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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Brooklyn Clinical Research — Brooklyn
Identifiers
NCT: NCT06412536 · CORE042024