- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05321914
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:
- Compare the effects of resistance exercise training performed in the morning vs the evening on insulin sensitivity
- Compare the effects of resistance exercise training performed in the morning vs the evening on gains in muscle mass and strength
- 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
-
-
-
Glasgow, United Kingdom
- Stuart Robert Gray
-
-
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.
Sponsor
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
Keywords
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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