Extended daily fasting, regulation of energy balance and associated health outcomes: a randomised single centre intervention study with two phases

niversity of Bath (UK)0 sites70 target enrollmentStarted: November 3, 2010Last updated: March 30, 2020

Conditions

Trial Snapshot

•1. Participants may be male or female (females may or may not be taking oral contraceptives but must maintain a record of menstrual cycle phase or contraceptive use prior to entry into the study)
•2. Those within the specified age range (20 - 60 years)
•3. Individuals with a body mass index between 20 - 24 kg/m2 or above 30 kg/m2
•4. Able and willing to safely comply with all study procedures
•5. Able to provide written informed consent for participation whilst acknowledging their freedom to withdraw at any point during the study

•1. Women who are known to be pregnant or who are intending to become pregnant over the course of the study
•2. Women who are breast feeding
•3. Participation in another clinical trial
•4. Any reported use of substances which may pose undue personal risk to participants or introduce bias into the experiment
•5. Any other condition or behaviour deemed either to pose undue personal risk to the participant or introduce bias into the experiment
•6. Individuals with any known bleeding disorder
•7. Individuals currently taking any medication known to act as an anticoagulant

Sponsor

niversity of Bath (UK)