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NCT05505305Completed

Time-restricted Eating and Interval Training With Digital Follow-up

Effects of Time-restricted Eating and Interval Training With Digital Follow-up: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 21 Jun 2024

Brief summary (registry, in English)

This study will investigate the effects of seven weeks of time-restricted eating combined with high-intensity interval training compared with a control group on body composition in adults with overweight/obesity. Participants in the intervention group will complete the intervention remotely and will receive weekly follow-up through online platforms (telephone, video call). Before and after the intervention, the investigators will measure the participants' body composition, physical fitness, fasting blood glucose and insulin, blood lipids, and blood pressure. Physical activity, diet, sleep quality, appetite, and adherence to the intervention will also be measured. Secondary sub-analyses of sex differences in the responses to the intervention will be performed.

Status (registry)
Completed
Study type
Interventional
Enrollment
52 (actual)
First submitted
16 Aug 2022
Start date
1 Sept 2022
Primary completion date
13 May 2024
Lead sponsor
Norwegian University of Science and Technology
Diseases
Obesity
NCT number
NCT05505305

What you commit to

  • Study type: Interventional
  • Participants enrolled: 52
  • From 1 Sept 2022 to the primary completion date, 13 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Body mass variation ≥ 4 kg three months prior to study commencement

Other illness

  • Known diabetes mellitus (type 1 or 2) or cardiovascular disease

Lab values

  • Taking hypertension, glucose-, or lipid-lowering drugs

Other

  • On-going pregnancy
  • Lactation within 24 weeks of study commencement
  • High-intensity exercise ≥ 1/week
  • Habitual eating window ≤12 hours/day
  • Working night shifts

Who the study is looking for

  • Body mass index ≥ 27 kg/m²
  • Able to walk or ride a bike \> 60 min

Age in the registry: 18 years to 50 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of circulation and medical imaging, NTNU
Coordinator of this site? Confirm its status
TrondheimNorwayUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.