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ZOE-AFFIRM: Relative Validation of a Novel Food Frequency Questionnaire

Relative Validation of a Remote Novel Food Frequency Questionnaire Compared to 24hr Recalls in the ZOE AFFIRM Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05612997
Enrollment
80
Registered
2022-11-14
Start date
2022-11-08
Completion date
2022-12-20
Last updated
2022-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diet Habit

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.

Detailed description

Research Question: What is the relative validity of a novel FFQ (Food Frequency Questionnaire) compared to a widely accepted 24h dietary recall tool in a remote setting? Research Aim: This study aims to relatively validate the ZFFQ (ZOE Food Frequency Questionnaire; ZOE Ltd) by assessing its agreement with a widely accepted 24h diet recall tool, Intake24 (Newcastle University) in a remote population. Design: This study will be conducted in a single-arm design with the intake period under assessment comprising one month. 1. Participants will complete two periods of 3 consecutive days each (one weekend-day and two weekdays, i.e. Sunday-Tuesday or Thursday-Saturday), in which they will complete 6 total rounds of Intake24 (one completion per previous 24 hours). The two periods must be at least 14 days apart; participants will be given multiple options of dates to choose from in November/December that satisfy these requirements. 2. Once the two recall periods are completed, the participant will be asked to fill out the ZFFQ recalling food frequency (without portion sizes) over the preceding month (which encompasses the two recall periods). Population: In brief, participants are generally healthy UK-based adults who provided consent to participation in this remote study. Please see the eligibility section for full criteria. Participants provided consent before undertaking any study procedures. Data analysis: Agreement analysis will be used to compare both dietary assessment methods and evaluate the relative validity of the ZOE FFQ. Data collection: * Baseline demographic data (age, sex, BMI, ethnicity, smoking, socio-economic status) * Dietary data (FFQ and 24hr dietary recall)

Interventions

OTHERDietary Assessment

Food Frequency Questionnaire and 24h Recalls.

Sponsors

Zoe Global Limited
CollaboratorOTHER
King's College London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 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

Exclusion criteria

\- Do not meet the inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Food Frequency Questionnaire30 days
24h Recalls6 days

Countries

United Kingdom

Contacts

Primary ContactEmily R Leeming, PhD
emily.leeming@kcl.ac.uk07791131380
Backup ContactInbar Linenberg, MS
inbar.linenberg@kcl.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026