Clinical Trials Directory

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UnknownNCT03650127

Returning Genome and Metabolome Data to FinTerveys 2017 Participants: P5.fi FinTerveys Study

Returning Genome and Metabolome Data to FinTerveys 2017 Participants: P5.fi

Status
Unknown
Phase
Study type
Observational
Enrollment
3,449 (actual)
Sponsor
Markus Perola · Other Government
Sex
All
Age
Healthy volunteers
Accepted

Summary

P5.fi study - P4 together with a fifth 'P' and '.fi' for population health Finally Implemented in Finland - studies the value of returning genetic and metabolomic risk information in two diseases (coronary heart disease and type 2 diabetes) and one feature (venous thromboembolism). The hypothesis of the study is that 1) combining genetic and metabolic risk with traditional risk factors adds value to the personal risk assessment of these diseases, 2) such risk information can be provided to individuals using a web based user portal in an easily understandable and useful format, and 3) receiving genetic and metabolomic risk information has an effect on the health of the study participants. The study is a continuation of FinHealth 2017 -study, which involved more than 7,000 Finns from around the country. The participants of FinHealth were invited to participate in P5.fi -study. The new research utilises information, samples, and measurements obtained in the FinHealth Study. Prospective clinical significance of selected genetic and metabolomic risk scores will be studied in 30.000 Finnish individuals. The study will analyze the genetic and metabolomic profile of the P5.fi participants and develop and test a protocol for returning them health related risk information. The impact of the intervention will by followed up by questionnaires and national health registers for five years.

Conditions

Timeline

Start date
2018-02-02
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2018-08-28
Last updated
2021-01-15

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT03650127. Inclusion in this directory is not an endorsement.