Investigating the Impact of Early Time-Restricted Eating on Health Outcomes and Quality of Life in Adults With Mild Controlled Asthma Compared to Healthy Adults
This study aims to explore how early time-restricted eating (eTRE) - where all daily meals are eaten within a specific time window - affects health and quality of life in adults. The researchers will compare results between adults with mild, well-controlled asthma and adults without asthma (non-asthma group). Participants can continue to eat their normal food; only the timing of meals will change.
Conditions studied
Asthma Management, Time Restricted Eating
About this study
This study aims to explore how early time-restricted eating (eTRE) - where all daily meals are eaten within a specific time window - affects health and quality of life in adults. The researchers will compare results between adults with mild, well-controlled asthma and adults without asthma (non-asthma group). Participants can continue to eat their normal food; only the timing of meals will change.
Interventions
- Other: Early Time-Restricted Eating (eTRE) and Habitual Diet (HD) — The participants who are assigned to eTRE will be asked to eat from 8 am to 4 pm without restriction on the quantity or amount of food and fast for the rest of the time except for drinking water for one week. After a minimum of two weeks washout period, participants will be asked to follow their habitual diet for one week.
- Other: Habitual Diet (HD) and Early Time-Restricted Eating (eTRE) — The participants will be asked to follow their habitual diet for one week. After a minimum of two weeks washout period, the participants will be assigned to eTRE and asked to eat from 8 am to 4 pm without restriction on the quantity or amount of food and fast for the rest of the time except for drinking water for one week.
Primary outcomes
- Lung Function Parameters, FEV1 in Liters (L) (At baseline and after 1 week in each study arm)
- Lung Function Parameters, FVC in Liters (L) (At baseline and after 1 week in each study arm)
- Lung Function Parameters, FEV1/ FVC ratio (At baseline and after 1 week in each study arm)
Eligibility information
Study locations
- Health and Life Science, Leicester, England United Kingdom
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.