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Genetic Information and Dietary Intake Behaviour

U

University of Toronto

Status and phase

Completed
Early Phase 1

Conditions

Healthy

Treatments

Other: Dietary advice with genetic information
Other: General dietary recommendations

Study type

Interventional

Funder types

Other

Identifiers

NCT01353014
AElSohemy

Details and patient eligibility

About

This study's primary objective is to determine if providing individuals with personal genetic information impacts dietary intake behaviour. Specifically, the investigators will be examining whether providing dietary advice based on genes that affect the metabolism of or sensitivity to caffeine, vitamin C, sugar and sodium will impact the intake of these dietary components. The study hypothesis is that providing dietary advice based on genetics will impact dietary behaviour to a greater extent than general dietary recommendations.

Enrollment

138 patients

Sex

All

Ages

20 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 20-35 year old participants from the Toronto Nutrigenomics and Health Study

Exclusion criteria

  • pregnancy or nursing
  • vitamin C supplement users
  • caffeine intake < 100 mg/day
  • total sugars intake < 10% energy
  • sodium intake < 1500 mg/day

Trial design

138 participants in 2 patient groups

Dietary advice with genetic information
Experimental group
Description:
This group will receive dietary advice for caffeine, vitamin C, sugar and sodium based on genetic information.
Treatment:
Other: Dietary advice with genetic information
General dietary recommendations
Active Comparator group
Description:
This group will receive general dietary recommendations for caffeine, vitamin C, sugar and sodium from recognized health institutions (caffeine: Health Canada; sugar: the World Health Organization; vitamin C and sodium: the Institute of Medicine).
Treatment:
Other: General dietary recommendations

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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