NCT02948517.

Methods	Randomised controlled trial
Participants	31 participants Ages eligible for study: 25 years to 65 years (adult, older adult) Sexes eligible for study: all Accepts healthy volunteers: yes Criteria Inclusion Criteria: Male or female Body mass index (BMI) between 30.0 and 40 kg/m2 Age between 25 and 65 years Sedentary (light exercise less than 1 hour per week) or moderately active (moderate exercise 1 to 2 hours per week) Weight stable for >3 months prior to the beginning of the study (gain or loss <4 kg) Able to give written informed consent
Interventions	Arm Intervention/treatment Experimental: Time restricted feeding Time restricted feeding Other: Time restricted feeding Time restricted feeding No Intervention: Control No intervention
Outcomes	Primary outcome measures: Body weight [ Time Frame: 12 weeks ] Secondary outcome measures: Plasma lipids [ Time Frame: 12 weeks ] Blood pressure [ Time Frame: 12 weeks ] Insulin resistance measured by Homeostatic model assessment (HOMA) [ Time Frame: 12 weeks ] Inflammatory markers: tumour necrosis factor‐alpha (TNF) and Interleukin‐6 (IL‐6) [ Time Frame: 12 weeks ]
Notes	NCT02948517‐ It is unclear from the information above that the intervention meets our predefined criteria.