Resistance Exercise, Metabolism and Time of Day

Sponsor
University of Glasgow (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05321914
Collaborator
(none)
36
1
3
23
1.6

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Impact of the Time of Day on Metabolic Responses to Resistance Exercise in Adults Who Are Obese or Overweight: a Randomised Controlled Trial
Anticipated Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

Habitual physical activity

Experimental: Morning exercise

Exercise training in the morning (6:00-10:00am)

Behavioral: Exercise training
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)

Behavioral: Exercise training
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.

Outcome Measures

Primary Outcome Measures

  1. Change in insulin sensitivity [Change from baseline to 6 weeks]

    Insulin sensitivity calculated via the Matsuda Index during an oral glucose tolerance test

Secondary Outcome Measures

  1. Change in vastus lateralis muscle thickness [Change from baseline to 6 weeks]

    Muscle thickness of the vastus lateralis muscle measured via ultrasound

  2. Change in whole body lean mass [Change from baseline to 6 weeks]

    whole body lean mass measured via bio-electrical impedance

  3. Change in whole body fat mass [Change from baseline to 6 weeks]

    whole body fat mass measured via bio-electrical impedance

  4. Change in one-repetition maximum muscle strength [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

  5. Change in knee extensor maximal isometric torque [Change from baseline to 6 weeks]

    Knee extensor maximal isometric torque measured during a maximal voluntary contraction

  6. Change in grip strength [Change from baseline to 6 weeks]

    Grip strength measured with a hand held dynamometer

  7. Change in mean glucose levels [Change from baseline to 6 weeks]

    Mean glucose levels measured via continuous glucose monitors

  8. Change in glucose variability [Change from baseline to 6 weeks]

    Glucose variability measured via continuous glucose monitors

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stuart Robert Gray Glasgow United Kingdom

Sponsors and Collaborators

  • University of Glasgow

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stuart Gray, Senior Lecturer, University of Glasgow
ClinicalTrials.gov Identifier:
NCT05321914
Other Study ID Numbers:
  • 200210068
First Posted:
Apr 11, 2022
Last Update Posted:
Apr 11, 2022
Last Verified:
Apr 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Stuart Gray, Senior Lecturer, University of Glasgow
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 11, 2022