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Extend (The Exeter 10,000 project)

Population Size

0

People

Population Size statistic card

Years

2010

Years statistic card

Associated BioSamples

None/not available

Associated BioSamples statistic card

Geographic coverage

United Kingdom

Geographic coverage statistic card

Lead time

Data only
Lead time statistic card

Summary

he EXTEND Cohort Study 10,000 is a large-scale, longitudinal research project designed to investigate a wide range of health and lifestyle factors in the general population. It aims to collect data from 10,000 participants to explore the relationships between genetic, environmental, and lifestyle factors and the development of diseases, particularly focusing on chronic diseases like cardiovascular conditions, diabetes, cancer, and mental health disorders.

Documentation

A re-contactable research volunteer register and sample biobank of local people with and without health problems who are willing to provide blood and urine samples, have their blood pressure taken and answer simple health and lifestyle questions. Half of the sample taken is used to measure diagnostic markers including blood sugar and cholesterol, which can be shared with the volunteer and the remaining half (requiring consent from the participant) is saved in a biobank. Participants without diabetes will be offered the opportunity to receive a copy of their health measures and blood tests. They may also choose to have these results copied to their doctor. Participants are invited to a return visit (after around three years) to replace samples that have been used up, and update the measurements and other health data recorded The Peninsula Research Bank (PRB) holds the data and banked samples of DNA, urine, serum, plasma and prospectively collected RNA/ whole blood for long term management. The Extend/PRB Biobank enables research into why some people are predisposed to develop a disease as they get older and why some people are protected. The EXTEND register volunteers who are identifiable by phenotype and genotype and agree that they can be contacted to participate in various research projects based on their genetic predisposition have the choice of whether they wish to be involved in studies about Dementia/Alzheimer's disease. Participants can give permission for Researchers to access their medical records.

Dataset type

Health and disease

Dataset sub-type

Not applicable

Keywords

Provenance

Purpose of dataset collection

Research cohort

Biological sample availability

None/not available

Structural Metadata

Details

Publishing frequency

Continuous

Version

1.0.0

Modified

17/02/2025

Coverage

Start date

23/03/2010

Time lag

Not applicable

Geographic coverage

United Kingdom

Follow-up

Continuous

Accessibility

Language

en

Alignment with standardised data models

OTHER

Controlled vocabulary

OTHER

Format

CSV

Data Access Request

Dataset pipeline status

Available

Access method category

TRE/SDE

Access service description

The Data Portal runs its analysis environment through a virtual desktop infrastructure accessible via VMWare software. By analysing the data in the virtual desktop environment you are working on DPUK's servers – meaning there is no physical transfer of data to researchers. The processing capacity enables you to work with large numbers of records and integrate these with the other data modalities that exist in the DPUK cohorts. This solution also offers researchers the freedom to conduct their analyses anywhere with an internet connection.

Data Controller

University of Exeter Medical School in partnership with the Royal Devon and Exeter NHS Foundation Trust

Data Processor

Dementias Platform UK

Dataset Types: Health and disease


Collection Sources: