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The Feasibility of Early Time-Restricted Eating in a Student Population

The Feasibility of Early Time-Restricted Eating in a Student Population

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05750277
Enrollment
16
Registered
2023-03-01
Start date
2023-04-19
Completion date
2023-05-19
Last updated
2023-04-24

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

Conditions

Intermittent Fasting, Time Restricted Feeding

Keywords

Students, Metabolism, Appetite

Brief summary

This study proposes to investigate the effect of a self-selected early time-restricted eating window in University students.

Detailed description

There were over 2.3 million students registered at Higher Education institutes in the UK. Early adulthood is a critical time for establishing self-care habits which will ultimately influence health outcomes later in adulthood and studies suggest that the overall health of students is poor relative to that of their age-matched peers not in education. Therefore, the investigators would like to assess the feasibility of adopting a novel, nutritional intervention in this important, understudied population. Previous research has shown Early Time-Restricted Eating can reduce daily energy consumed and improve markers of health over time, in a range of populations. Therefore, the investigators are investigating how often participants can eat within an early 8 hour eating window, starting no earlier than 8am (finishing calorie intake by 4pm), or no later than 10am (finishing calorie intake by 6pm). The investigators will be measuring how often the participants can adhere to this eating window between Monday to Friday, with the study lasting 4 weeks in total. This is a feasibility study, so this study will investigate whether this intervention is achievable and what social barriers may exist which reduce adherence to this eating window. Participants will visit the laboratory on 3 occasions (at the start, halfway point, and at the end of the intervention) to measure any changes in health markers across the intervention. The lab visits will involve providing a finger-tip blood sample, and measuring body mass, blood pressure, and waist-to-hip circumference. Outside of the laboratory, participants are required to record their eating window on a mobile app and an investigator-created trial sheet. Further measures outside of the laboratory will include a weekly questionnaire and motivational correspondence via mobile text message.

Interventions

OTHEREvening Time-Restricted Eating

Eating between 8am-6pm.

Sponsors

Nottingham Trent University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Registered student

Exclusion criteria

* Not taking any medication which is known to affect appetite

Design outcomes

Primary

MeasureTime frameDescription
Successful bouts of Early Time-Restricted Eating4 weeksSuccessful Early Time-Restricted Eating occasions will be recorded by the participant on a mobile device and an investigator-created trial sheet.

Secondary

MeasureTime frameDescription
Insulin4 weeksHow their Insulin concentrations change over the trial
HbA1C4 weeksHow their HbA1CA concentrations change over the trial
Body mass4 weeksHow their body mass changes over the trial
Glucose4 weeksHow their glucose concentrations change over the trial
Body fat percentage4 weeksHow their body fat percentage changes over the trial
Waist to hip ratio4 weeksHow their waist to hip ratio changes over the trial
Appetite4 weeksInvestigators will record appetite sensations, such as; hunger, fullness, prospective food consumption, desire to eat and nausea. Investigators will record these validated sensations to observe any changes across the trial. A visual analogue scale (100mm) will be digitised and sent to the participant by mobile text to record changes in the aforementioned appetitte sensations.
Blood pressure4 weeksHow blood pressure (systolic and diastolic) changes over the trial

Countries

United Kingdom

Outcome results

None listed

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