Survey to determine eligibility for cardiovascular and obesity clinical trials
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility (SWIFT-CORE-101)
This study is trying to see if people with heart issues or obesity can join new clinical trials by having them fill out a survey and undergo some health checks.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Brooklyn Clinical Research Research network |
| Locations | 1 site (Brooklyn, New York) |
| Trial ID | NCT06412536 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the eligibility of potential participants for industry-sponsored clinical trials focused on cardiovascular diseases, obesity, and related endocrine conditions. Participants will undergo a survey that includes demographic information, medical history, and current symptoms, overseen by a physician. Vital signs, urine drug screens, blood draws, and urine pregnancy tests may also be collected to evaluate suitability for participation. The physician will conduct a clinical interview and may consult with the participant's current healthcare providers to confirm eligibility.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are interested in participating in clinical trials for cardiovascular diseases and obesity-related conditions.
Not a fit: Patients who are pregnant, breastfeeding, or have significant health issues that could affect their safety or study results may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could streamline the process of identifying eligible patients for clinical trials, potentially leading to improved treatment options for cardiovascular and metabolic conditions.
How similar studies have performed: While this approach is observational and focused on eligibility assessment, similar studies have successfully identified participants for clinical trials in related fields.
Eligibility criteria
Show full inclusion / exclusion 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 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.
Where this trial is running
Brooklyn, New York
- Brooklyn Clinical Research — Brooklyn, New York, United States (Recruiting)
Study contacts
- Principal investigator: Ammara Mushtaq, MD — Brooklyn Clinical Research
- Study coordinator: Ammara Mushtaq, MD
- Email: amushtaq@brooklynclinicalresearch.com
- Phone: 929-203-5879
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.