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The INTERVAL study

Public Health and Primary Care

Header Left

Interval Study logo, including the words "Interval"

Header Left

Interval Study logo, including the words "Interval"
  • Home
  • About
    • About the study
    • Why is it important?
    • What is involved?
    • Who’s involved?
    • Where?
    • Information leaflet
    • Consent form
    • Electronic Health Record Linkage
  • FAQs
    • INTERVAL Main Results
    • General questions from INTERVAL donors
    • 2-year anniversary measurements
    • Physical Activity measurements
    • INTERVAL Phase II
    • INTERVAL Phase III
    • Accessing Electronic Health Records
  • Physical Activity
  • Phase II & III
    • INTERVAL Phase II
    • INTERVAL Phase III
  • Contact Us
  • Publications
  • News
  • Home
  • About
    • About the study
    • Why is it important?
    • What is involved?
    • Who’s involved?
    • Where?
    • Information leaflet
    • Consent form
    • Electronic Health Record Linkage
  • FAQs
    • INTERVAL Main Results
    • General questions from INTERVAL donors
    • 2-year anniversary measurements
    • Physical Activity measurements
    • INTERVAL Phase II
    • INTERVAL Phase III
    • Accessing Electronic Health Records
  • Physical Activity
  • Phase II & III
    • INTERVAL Phase II
    • INTERVAL Phase III
  • Contact Us
  • Publications
  • News

What is involved?

  • Being asked to attend donation appointments either at standard intervals between donations (i.e. 12 weeks for men and 16 weeks for women) or reduced intervals (i.e. either 10 or 8 weeks for men and 14 or 12 weeks for women) over a two-year period.
  • Giving a small sample of blood for research purposes on your enrolment to the study and after two years.  This will not involve any additional needles.
  • Completing online questionnaires every six-months during the study.
  • Agreeing to give the INTERVAL study team permission to access your medical and other health-related records and for long-term anonymised storage and use of this information for future ethically-approved health-related research purposes.
  • Agreeing to have your samples, questionnaire data, health-related and other information stored by the INTERVAL study team and used, for many years, in an anonymous form by researchers for a broad range of ethically-approved scientific health studies.
  • Being contacted, no more than three times a year, by the INTERVAL study team about further studies organised by NHSBT and/or the Universities of Cambridge and Oxford.

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