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NCT03277365 · ClinicalTrials.gov registry record · NA

MyGeneRank: A Digital Platform for Next-Generation Genetic Studies

A NA study of Heart Diseases, sponsored by Scripps Translational Science Institute.

Recruiting
Registry status
NA
Development phase
100,000
Enrollment target
1
Study location

NCT03277365 is a NA study of Heart Diseases that is actively recruiting participants, run by Scripps Translational Science Institute. The registered enrollment target is 100,000 participants, above the 4,356-participant average among 85 other Heart Diseases trials with a reported enrollment target (2196% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT03277365, a NA study of Heart Diseases, is actively recruiting participants, sponsored by Scripps Translational Science Institute.

RECRUITING
Registry status
NA
Development phase
100,000 participants
Enrollment target
1
Study location

Study Summary

Many conditions affecting health are caused by a combination of environment, behaviors, and genes. While individuals can alter some factors in their lives to reduce the chances of developing different diseases (e.g., not smoking cigarettes), the contribution from genetic risk encoded by DNA remains with people throughout their lives. Scientists are still trying to determine the entirety of genetic factors that influence disease, but for some conditions it has been shown that the factors identified thus far can begin to identify people at high to low genetic risk. Looking across the genome, scientists can calculate a cumulative genetic risk score - which can be used to rank genetic risk compared to other worldwide populations. The goal of this study is to determine how genetic risk influences health decisions and other things that can be controlled in life. The first genetic risk score is calculated for coronary heart disease (CAD). CAD ultimately leads to heart attacks, heart failure and sometimes sudden cardiac death and is the main reason heart disease remains as the number one cause of death worldwide. Other researchers have shown that this genetic risk score can be used to identify people with low, intermediate, and high risk for coronary heart disease. It has also been shown that the use of statins (cholesterol lowering drugs) provides greater benefit and protection against heart attack for people with high genetic risk for coronary artery disease. Leveraging the Apple ResearchKit and the ResearchKit linked 23andMe API, customers of 23andMe are able to provide researchers access to their genomic data. Participants will use the ResearchKit app to provide consent, view study information, answer surveys, and contact the study team. Participants will be asked to complete 3 surveys. One before viewing genetic risk scores, one immediately after viewing scores, and one 6 months after viewing scores.

Conditions Studied

Interventions

  • OTHER Receive genetic risk information

Study Locations (1)

California

  • Scripps Translational Science Institute - La Jolla

Trial Details

FieldValue
Enrollment Target 100,000 participants
Start Date 2017-09-26
Est. Completion 2030-09
Phase NA

What the Registry Record Tells You About NCT03277365

The ClinicalTrials.gov registry entry for NCT03277365 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100,000 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 4,356-participant average among 85 other Heart Diseases trials with a reported enrollment target (2196% higher). The listed sponsor is Scripps Translational Science Institute, which has 41 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Diseases appearing as the primary indexed condition, and to 1 intervention - of which Receive genetic risk information is the first listed.

NCT03277365 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT03277365 about?

NCT03277365 is a clinical study titled "MyGeneRank: A Digital Platform for Next-Generation Genetic Studies". Many conditions affecting health are caused by a combination of environment, behaviors, and genes. While individuals can alter some factors in their lives to reduce the chances of developing different diseases (e.g., not smoking cigarettes), the contribution from genetic risk encoded by DNA remains ...

What is the current status of trial NCT03277365?

This trial is currently recruiting. It is a NA study. The enrollment target is 100,000 participants. The study started on 2017-09-26. Estimated completion is 2030-09.

What conditions does trial NCT03277365 study?

This clinical trial studies the following conditions: Heart Diseases.

What interventions are being tested in trial NCT03277365?

The interventions under investigation include: Receive genetic risk information (OTHER).

Who is sponsoring clinical trial NCT03277365?

This trial is sponsored by Scripps Translational Science Institute, which has 41 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03277365 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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