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

Description

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.

Conditions

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

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Study Overview

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Study Details

Study 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.

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

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

Condition
Cardiovascular Diseases
Intervention / Treatment

-

Contacts and Locations

Brooklyn

Brooklyn Clinical Research, Brooklyn, New York, United States, 11226

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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.
  • 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Brooklyn Clinical Research,

Ammara Mushtaq, MD, PRINCIPAL_INVESTIGATOR, Brooklyn Clinical Research

Study Record Dates

2029-04-17