ZOE Health Study: The Intermittent Fasting Study

Intermittent Fasting Clinical Trial

Official title:

The Intermittent Fasting ZOE Health Study: Effects on Hunger, Mood, Energy and Symptom Burden in a UK Cohort

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05558423
• Other study ID #: ZHS-IF
• Status: Recruiting
• Phase: N/A
• Start date: October 24, 2022
• Est. completion date: October 24, 2023

Study information

• Verified date: September 2022
• Source: Zoe Global Limited
• Contact: Christina Hu
• Phone: 07950 335916
• Email: zoehealthstudy[@]kcl.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150000
• Est. completion date: October 24, 2023
• Est. primary completion date: October 24, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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:

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

Exclusion Criteria:

• Unable to provide written informed consent

Related Conditions & MeSH terms

• Intermittent Fasting
• Time Restricted Feeding

Intervention

Behavioral:
• Time Restricted Eating
Participants are asked to follow a Time Restricted Eating regimen with eating window of =10 hours.

Locations

Country	Name	City	State
United Kingdom	ZOE Limited	London

Sponsors (2)

Lead Sponsor	Collaborator
Zoe Global Limited	King's College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	TRE window clock time	The chosen clock time for the TRE window (early, vs. middle, vs. late)	2 weeks
Primary	Habitual eating window clock time	The chosen clock time for the habitual eating window	1 weeks
Primary	Hunger	Hunger levels reported by visual analogue scale ("how hungry did you feel yesterday?"; 0-10; where 10 is the most hungry)	3 weeks (plus optional unlimited weeks)
Primary	Mood	Mood levels reported by visual analogue scale ("how was your mood yesterday?"; 0-10; where 10 is most positive)	3 weeks (plus optional unlimited weeks)
Primary	Energy	Energy levels reported by visual analogue scale ("how energetic did you feel yesterday?"; 0-10; where 10 is most energetic)	3 weeks (plus optional unlimited weeks)
Primary	Symptom burden	The self-reported symptom burden while completing both habitual and TRE phases	3 weeks (plus optional unlimited weeks)
Secondary	Body weight	Self-reported in the study app (optional)	3 weeks (plus optional unlimited weeks)
Secondary	Gastrointestinal symptoms	Gastrointestinal symptoms self-reported by questionnaire	3 weeks (plus optional unlimited weeks)
Secondary	Eating habits	Eating habits self-reported by questionnaire, including number of main meals and snacks per day	3 weeks (plus optional unlimited weeks)