NCT05612997

Brief Summary

Dietary assessment is critical for dietary research. Food Frequency Questionnaires (FFQ) measure habitual dietary intake and are low user and researcher burden. The ZOE AFFIRM study aims to assess the relative validity of a novel FFQ compared to a widely accepted 24h dietary recall tool in a remote setting.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 4, 2022

Completed
4 days until next milestone

Study Start

First participant enrolled

November 8, 2022

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 14, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 20, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2022

Completed
Last Updated

November 14, 2022

Status Verified

October 1, 2022

Enrollment Period

1 month

First QC Date

November 4, 2022

Last Update Submit

November 4, 2022

Conditions

Diet Habit

Outcome Measures

Primary Outcomes (2)

  • Food Frequency Questionnaire

    30 days

  • 24h Recalls

    6 days

Study Arms (1)

Relative Validation Arm

Other: Dietary Assessment

Interventions

Dietary AssessmentOTHER

Food Frequency Questionnaire and 24h Recalls.

Relative Validation Arm

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

United Kingdom-based adult population who have subscribed to the ZOE Product waitlist.

You may qualify if:

  • Can provide written informed consent
  • Are willing and able to comply with all study protocols
  • Are willing to complete their dietary recall periods on specified dates
  • Have BMI 18 and above
  • Are any sex
  • Are aged 18 years old and above
  • Live in England, Scotland, Wales or Northern Ireland

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

ZOE Ltd.

London, United Kingdom

Location

MeSH Terms

Conditions

Feeding Behavior

Interventions

Nutrition Assessment

Condition Hierarchy (Ancestors)

Behavior, AnimalBehavior

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationEpidemiologic MeasurementsPublic HealthEnvironment and Public Health

Study Officials

  • Sarah E Berry, PhD

    King's College London and Consultant at ZOE Ltd

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Emily R Leeming, PhD

CONTACT

07791131380emily.leeming@kcl.ac.uk

Inbar Linenberg, MS

CONTACT

inbar.linenberg@kcl.ac.uk

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 4, 2022

First Posted

November 14, 2022

Study Start

November 8, 2022

Primary Completion

December 20, 2022

Study Completion

December 20, 2022

Last Updated

November 14, 2022

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations

GB(1)