An Observational Study of Patients With Metabolic Syndrome and Related Conditions

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTarget PharmaSolutions, Inc.

About this trial

TARGET-METABOLIC is an observational research study to conduct a comprehensive review of outcomes for patients with metabolic syndrome and related conditions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Death

Manual removal (sponsor or site request)

No EHR interface encounter > 3 years

Adult patients diagnosed and managed for these conditions invited to participate

Trial population

The study will include adults with metabolic syndrome and related conditions.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

2,000,000 Participants
are grouped into 2 trial groups
Group A: Disease Cohort
Group B: Engaged Cohort

Trial outcomes

Primary outcomes

1

To characterize the natural history of disease in patients with metabolic syndrome and related conditions

A detailed analysis of available demographics, anthropometric characteristics, glycemic metrics, medications, co-morbidities, and medical history from sites across the US will inform the profile for various patient populations enrolled into the study. Collection of detailed medical records will be curated and analyzed to characterize disease natural history, clinical course of disease, number and types of interventions, current treatment paradigms, and the patient diagnostic journey. These data may also establish incidence rates of events of special interest. Collection of prospective medical records for each patient enables the continuation of these analyses longitudinally for changes and progression to characterize the clinical course of disease. The progression of pre-existing co-morbidities and variances across populations will also be evaluated.

Time frame
15 Years
2

To assess safety and effectiveness of treatments for metabolic syndrome and related conditions.

The study will evaluate the characteristics of patients receiving various treatments, effectiveness of treatment, and medical events that develop while receiving treatment for metabolic syndrome and related conditions. Treatments may be pharmacologic, surgical, procedures, radiologic or other interventions given to change the disease course/outcomes. Interval disease and medical events may vary depending on the patient's stage and type of disease and extent of co-morbidities at study entry and time of diagnosis.

Time frame
15 Years

Secondary outcomes

1

To evaluate provider management practices in the treatment of patients with metabolic syndrome and related conditions

Health care provider type, clinic setting, reason for initiating/not initiating/adjusting dosing of treatments or interventions (i.e., surgery, radiation), reason for discontinuing/switching treatments, and monitoring outcomes on and off treatment, will be captured as available in the provided EHR and/or through linked data. Disease-specific quality measures will be selected and evaluated, and the curated data can enable analyses to describe and evaluate healthcare utilization patterns.

Time frame
15 Years
2

To evaluate longitudinal and patient reported outcomes in patients with metabolic syndrome and related conditions

Longitudinal clinical outcomes and disease progression will be assessed. Self-reported patient health measures collect information directly from patients to measure physical, mental, and social health. These measures can help clinicians better understand how the disease state and/or various treatments affect what patients are able to do and the symptoms they experience beyond what is typically derived and reported in the EHR as part of traditional clinical evaluations. The information can also be used to help patients make informed decisions about their healthcare and treatment options.

Time frame
15 Years
3

To select and evaluate quality of care measures for patients with metabolic syndrome and related conditions

1. Identify deficiencies and select best practices in care of patients 2. Develop a technology infrastructure to evaluate quality measures to support clinicians.

Time frame
15 Years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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