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Clinical Trials/NCT05750277
NCT05750277
Active, not recruiting
Not Applicable

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

Nottingham Trent University1 site in 1 country16 target enrollmentApril 19, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Time Restricted Feeding
Sponsor
Nottingham Trent University
Enrollment
16
Locations
1
Primary Endpoint
Successful bouts of Early Time-Restricted Eating
Status
Active, not recruiting
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 19, 2023
End Date
May 19, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

William Mode

Principal Investigator

Nottingham Trent University

Eligibility Criteria

Inclusion Criteria

  • Registered student

Exclusion Criteria

  • Not taking any medication which is known to affect appetite

Outcomes

Primary Outcomes

Successful bouts of Early Time-Restricted Eating

Time Frame: 4 weeks

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

Secondary Outcomes

  • Insulin(4 weeks)
  • Body mass(4 weeks)
  • Blood pressure(4 weeks)
  • Body fat percentage(4 weeks)
  • Waist to hip ratio(4 weeks)
  • HbA1C(4 weeks)
  • Glucose(4 weeks)
  • Appetite(4 weeks)

Study Sites (1)

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