The Acute T-Rex (Timing of Resistance Exercise) Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-74
SponsorUniversity of Utah

About this trial

The primary aim of this study is to evaluate if a single bout of AM vs PM resistance exercise has different effects on insulin sensitivity and sleep. A randomized cross-over trial be used to compare resistance exercise at two different times of the day. Each condition will take place in a laboratory setting. Each condition will consist of exercise, overnight sleep, and oral glucose tolerance tests the following day. The AM exercise will occur \~1.5 hours after habitual wake, and PM exercise will occur \~11 hours after habitual wake. After a 2-6 week washout, participants will complete the other condition. The hypothesis is that PM exercise will be more beneficial than AM exercise in improving insulin sensitivity. This study could identify if there is a better time of day to perform resistance exercise to decrease risk of developing Type 2 Diabetes Mellitus.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Men and women, all ethnicities, aged 50-74 years

BMI ≥25 kg/m² and <45 kg/m²

Weight stable (less than 5% change in the past 6 months)

Generally healthy individuals

Disqualifiers

Uncontrolled cardiovascular, metabolic, renal, or pulmonary disease

Cancer treatment in the past 5 years

Untreated thyroid disease or other medical conditions affecting weight or energy metabolism

Current use of weight loss medication or other medications likely to impact energy balance

Trial design

Design model

Crossover

Treatments tested in this trial

  • Resistance Exercise Timing

    Behavioral

    1 resistance exercise session consisting of 3 sets, 10 repetitions per set, on 12 different exercises

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: AM Resistance ExerciseExperimental treatment 1 intervention
Group B: PM Resistance ExerciseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Insulin sensitivity

Insulin sensitivity will be calculated using the Matsuda Insulin Sensitivity Index

Time frame
1 day

Secondary outcomes

1

Sleep Duration

Sum of time spent in stage 1, stage 2, stage 3 and rapid eye movement stage (REM) as assessed via polysomnography.

Time frame
1 day

Other outcomes

1

Sleep Staging

Time spent in stage 1, stage 2, stage 3 and REM sleep assessed by polysomnography.

Time frame
1 day
2

Sleep Quality

As assessed via Pittsburg Sleep Quality Index Questionnaire (scale:0-21, higher scores=worse outcome) and polysomnography

Time frame
1 day
3

Sleep Efficiency

Ratio of time in bed vs time asleep

Time frame
1 day
4

Muscular Strength

Muscular strength as assessed via 10 repetition maximum test

Time frame
1 day

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