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Recruiting

NCT Number: NCT06412536

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

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.

Recruiting

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Key information

Conditions

Cardiovascular Diseases Body Weight Diabetes Mellitus Diabetes Mellitus, Type 2 Diabetes Type 2 Endocrine System Diseases Glucose Metabolism Disorders Hyperinsulinism Insulin Resistance Metabolic Diseases Metabolic Syndrome Nutrition Disorders Nutritional and Metabolic Diseases Obesity Overnutrition Overweight Pathological Conditions, Signs and Symptoms PreDiabetes Prediabetic State Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Brooklyn Clinical Research

Brooklyn, New York, 11226, United States

Location status: Recruiting

Location contact

Ammara Mushtaq, MD

CONTACT

[email protected]

929-203-5879

Ammara Mushtaq, MD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Blood Work

Other

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

Primary outcomes

  1. Number of participants who are interested in industry-sponsored clinical research

    Time frame: 5 years

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

Secondary outcomes

  1. Characteristics associated with patient populations interested in clinical trials

    Time frame: 5 years

    Characteristics associated with patient populations interested in clinical trials stratified by demographics and therapeutic areas

Study contacts

Contact information is provided by the study sponsor or research team.

Ammara Mushtaq, MD

CONTACT

[email protected]

929-203-5879

Katherine Azer, MS

CONTACT

[email protected]

929-332-7848

Sponsors and collaborators

Lead sponsor

Brooklyn Clinical Research

Network

Registry information

Official study title

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

Acronym: SWIFT-CORE-101

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
May 14, 2024
Registry last updated
Jun 11, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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