Resistance Exercise, Metabolism and Time of Day

March 25, 2025 updated by: Stuart Gray, University of Glasgow

The Impact of the Time of Day on Metabolic Responses to Resistance Exercise in Adults Who Are Obese or Overweight: a Randomised Controlled Trial

The aim of the current study is to determine the effect of time of day on the muscle and metabolic responses to resistance exercises in obese or overweight adults. To achieve this aim we have the following objectives:

  1. Compare the effects of resistance exercise training performed in the morning vs the evening on insulin sensitivity
  2. Compare the effects of resistance exercise training performed in the morning vs the evening on gains in muscle mass and strength
  3. Compare the acute glucose responses to resistance exercise performed in the morning vs the evening

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • pass the physical activity readiness questionnaire
  • body mass index (BMI) >27kg/m² and limited to 40 kg/m².

Exclusion Criteria:

  • Prior surgery for weight loss
  • Prior history of heart, lung, cancer, endocrine or liver disease
  • Participating in more than 1 hour structured exercise training per week

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Habitual physical activity
Experimental: Morning exercise
Exercise training in the morning (6:00-10:00am)
Exercise will consist of 1 set x 9 exercises x 3 sessions per week x 6 weeks. The load to be used during training will be calculated as 80% of one-repetition maximum (1RM) with each set performed to failure. 1RM will be re-tested on week 3, and the load adjusted accordingly, and upon completion of the study. During the training period, all sessions of training will be supervised by the researcher. The following exercises will be performed: Bench press, biceps curl, lat pull down, overhead press, lateral raise, leg extension, leg curl and calf raise.
Experimental: Evening exercise
Exercise training in the evening (4:00-8:00pm)
Exercise will consist of 1 set x 9 exercises x 3 sessions per week x 6 weeks. The load to be used during training will be calculated as 80% of one-repetition maximum (1RM) with each set performed to failure. 1RM will be re-tested on week 3, and the load adjusted accordingly, and upon completion of the study. During the training period, all sessions of training will be supervised by the researcher. The following exercises will be performed: Bench press, biceps curl, lat pull down, overhead press, lateral raise, leg extension, leg curl and calf raise.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in insulin sensitivity
Time Frame: Change from baseline to 6 weeks
Insulin sensitivity calculated via the Matsuda Index during an oral glucose tolerance test
Change from baseline to 6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in vastus lateralis muscle thickness
Time Frame: Change from baseline to 6 weeks
Muscle thickness of the vastus lateralis muscle measured via ultrasound
Change from baseline to 6 weeks
Change in whole body lean mass
Time Frame: Change from baseline to 6 weeks
whole body lean mass measured via bio-electrical impedance
Change from baseline to 6 weeks
Change in whole body fat mass
Time Frame: Change from baseline to 6 weeks
whole body fat mass measured via bio-electrical impedance
Change from baseline to 6 weeks
Change in one-repetition maximum muscle strength
Time Frame: Change from baseline to 6 weeks
Sum of one-repetition maximum of Bench press, biceps curl, lat pull down, overhead press, lateral raise, leg extension, leg curl and calf raise exercise
Change from baseline to 6 weeks
Change in knee extensor maximal isometric torque
Time Frame: Change from baseline to 6 weeks
Knee extensor maximal isometric torque measured during a maximal voluntary contraction
Change from baseline to 6 weeks
Change in grip strength
Time Frame: Change from baseline to 6 weeks
Grip strength measured with a hand held dynamometer
Change from baseline to 6 weeks
Change in mean glucose levels
Time Frame: Change from baseline to 6 weeks
Mean glucose levels measured via continuous glucose monitors
Change from baseline to 6 weeks
Change in glucose variability
Time Frame: Change from baseline to 6 weeks
Glucose variability measured via continuous glucose monitors
Change from baseline to 6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2022

Primary Completion (Actual)

February 1, 2024

Study Completion (Actual)

February 1, 2024

Study Registration Dates

First Submitted

April 1, 2022

First Submitted That Met QC Criteria

April 1, 2022

First Posted (Actual)

April 11, 2022

Study Record Updates

Last Update Posted (Actual)

March 30, 2025

Last Update Submitted That Met QC Criteria

March 25, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 200210068

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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