CClinicalTrials.gg
Status unknownNCT05558423Updated Nov 30, 2022

ZOE Health Study: The Intermittent Fasting Study

An interventional study of Time Restricted Eating in Intermittent Fasting and Time Restricted Feeding, sponsored by Zoe Global Limited. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-11-30.

Sponsored by Zoe Global Limited · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Sep 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
150,000
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The timing of food intake (chrononutrition) is emerging as a key regulator of circadian rhythm in metabolic organs. A wealth of research has been conducted on intermittent fasting, and time restricted eating (TRE) specifically, investigating the temporal patterns of diet (eating window, time of eating, time of largest energy intake) and their impact on disease risk, with overall beneficial impact on health. Studies have been conducted in a parallel or single arm design, while cross-over and the efficacy of TRE in ameliorating appetite and symptom burden within an individual remains unclear.

Read the detailed description

Time Restricted Eating (TRE; a type of intermittent fasting) is a dietary pattern based on the 24h day. Practicing individuals restrict their eating/feeding window to a certain number of hours, e.g. 4h, while the remaining hours in the day are non-feeding (fasting) time. The eating window is the duration of time from the start of the first meal to the end of the last meal in a 24 hr period. The eating window in a general population has previously been quantified at 12h (American cohort of n=15,000). It is important to note that TRE differs from other intermittent fasting protocols by (i) not specifying a change in dietary intake, such as requiring caloric restriction, but rather specifying the temporal pattern of intake; and (ii) requiring consistent daily eating windows over several days. TRE protocols can vary in the length of the eating window, as well as the anchoring of that window to the time of day, such that early vs. middle vs. late TRE regimens exist.

While the cardiometabolic benefits TRE are well established by human trials, other outcomes of dietary compliance remain unexplored and thus bring into question the sustainability of and adherence to TRE as a long-term dietary regimen. Perception of hunger, mood and energy, and self-elected timings of TRE eating windows while following the dietary pattern are not well understood. In particular, the relative differences in these outcomes between an habitual and a TRE eating pattern within the same individual must be determined in order to truly evaluate the acceptability of TRE on a per-individual basis.

The Intermittent Fasting Study, a sub-study of the ZOE Health Study (ZHS), will test the effects of habitual eating patterns vs. a TRE protocol on hunger, mood, energy and symptom burden in an adult UK cohort using the ZHS app.

Population:

This study is open to all participants currently enrolled in the ZHS study tracking physical and mental symptom burden on a daily basis. Participants will be invited to take part in the Intermittent Fasting Study and must provide their consent in order to participate.

Design:

The study will take place remotely using a n-of-1 design, consisting of two phases with a non-randomised cross-over. Firstly, the participant will complete a baseline phase of one week, where they follow their habitual eating pattern.

Secondly, for the second and third weeks of the study, the participant will be asked to follow a TRE regimen with an eating window of ≤10 hours. The exact duration of the eating window, its timing relative to time of day, and participant dietary intake, are decisions deliberately left to the participant for two reasons; (i) to enable the participant to choose exactly the right TRE protocol that is most acceptable to them and therefore most likely to be sustainable in the long-term; (ii) to understand the trends in acceptability and feasibility of TRE regimens across this UK cohort. The participant is given the option of continuing their TRE phase beyond the minimum two weeks.

During the two phases, participants are asked to log the following outcomes in the ZHS app, on a daily basis:

  • Hunger (using visual analogue scales, VAS)
  • Mood (using VAS)
  • Energy (using VAS)
  • Symptom burden (using VAS)
  • Body weight (optional)
  • Clock time of the start of their first eating event
  • Clock time of the end of their last eating event

Participants may also be asked to log their diet during their baseline phase and their TRE phase (optional) such that the temporal effect of changing between their habitual and chosen TRE regimens on dietary intake can be determined. They will also be asked to complete questionnaires, at the start and end of the study, about their eating habits, gastrointestinal health, lifestyle and demographic.

Outcome analysis may be stratified according to demographic and other exposure parameters such as early vs. late TRE.

02

Conditions studied

  • Intermittent Fasting
  • Time Restricted Feeding

Keywords

  • Intermittent Fasting
  • Time Restricted Eating
  • Hunger
  • Mood
  • Energy
03

In context

Lead sponsor

Zoe Global Limited is the lead sponsor of 8 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Participants on the ZOE Health Study (ZHS) app are accepted onto the study if they wish to participate and are within the UK.

The ZHS eligibility criteria are as follows:

Inclusion criteria

Inclusion Criteria:

  • Adults of 18 years and above, where the app has been approved for download from the Apple App and Google Play stores.

Exclusion criteria

Exclusion Criteria:

  • Unable to provide written informed consent
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
150,000 participants (estimated)

Study arms

  • Experimental
    Self-controlled

    n-of-1 design. Participants complete a baseline habitual eating phase following by an intervention TRE phase.

    Behavioral: Time Restricted Eating

Interventions

  • BehavioralTime Restricted Eating

    Participants are asked to follow a Time Restricted Eating regimen with eating window of ≤10 hours.

06

What researchers measure

Primary outcomes

  1. TRE window clock time

    The chosen clock time for the TRE window (early, vs. middle, vs. late)

    Time frame: 2 weeks

  2. Habitual eating window clock time

    The chosen clock time for the habitual eating window

    Time frame: 1 weeks

  3. Hunger

    Hunger levels reported by visual analogue scale ("how hungry did you feel yesterday?"; 0-10; where 10 is the most hungry)

    Time frame: 3 weeks (plus optional unlimited weeks)

  4. Mood

    Mood levels reported by visual analogue scale ("how was your mood yesterday?"; 0-10; where 10 is most positive)

    Time frame: 3 weeks (plus optional unlimited weeks)

  5. Energy

    Energy levels reported by visual analogue scale ("how energetic did you feel yesterday?"; 0-10; where 10 is most energetic)

    Time frame: 3 weeks (plus optional unlimited weeks)

  6. Symptom burden

    The self-reported symptom burden while completing both habitual and TRE phases

    Time frame: 3 weeks (plus optional unlimited weeks)

Secondary outcomes

  1. Body weight

    Self-reported in the study app (optional)

    Time frame: 3 weeks (plus optional unlimited weeks)

  2. Gastrointestinal symptoms

    Gastrointestinal symptoms self-reported by questionnaire

    Time frame: 3 weeks (plus optional unlimited weeks)

  3. Eating habits

    Eating habits self-reported by questionnaire, including number of main meals and snacks per day

    Time frame: 3 weeks (plus optional unlimited weeks)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 30, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05558423
Lead sponsor
Zoe Global Limited
Collaborators
King's College London
Responsible party
Sponsor
First posted
Sep 28, 2022
Start date
Oct 24, 2022
Primary completion
Oct 24, 2023 (estimated)
Completion
Oct 24, 2023 (estimated)
Last update
Nov 30, 2022

Study contacts

Christina Hu
Contact
zoehealthstudy@kcl.ac.uk
07950 335916
Tim Spector, Pr
principal investigator · Zoe Ltd, King's College London

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.

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