ClinicalTrials.gg
CompletedNCT07914361Updated Nov 3, 2026

Myo-Reps Versus Traditional Sets for Muscle Strength, Fat-Free Mass, and Time Efficiency

An interventional study of Myo-Reps resistance training and Traditional three-set resistance training in Resistance Exercise and Muscle Strength Development, sponsored by Norwegian University of Science and Technology. Completed at 1 site in Norway. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Aug 2025, registered Oct 2026).
Updated Nov 3, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This study compared two ways of doing strength training in healthy adults. The first, called Myo-Reps, is a time-saving method: one hard first set of 8-15 repetitions, followed by three short "mini-sets" of 3-5 repetitions with only 10-20 seconds of rest in between. The second is traditional training: three sets of 8-15 repetitions with 1-3 minutes of rest between sets.

Thirty-four adults were randomly assigned, by chance, to one of the two groups. For nine weeks everyone trained twice a week, under supervision, doing full-body workouts on 10 gym machines. The researchers measured how much stronger people became on each exercise, how much their fat-free mass (muscle and other lean tissue) changed, how hard the sessions felt, how much weight and how many repetitions were lifted, and how long the sessions took.

The aim was to find out whether the shorter Myo-Reps workouts can build strength and fat-free mass as well as traditional training.

Read the detailed description

Rationale: Lack of time is a common barrier to resistance training. The study tested two competing predictions. If total volume load (load × repetitions) is the main driver of adaptation, traditional three-set training should give greater improvements. If repetitions performed close to failure matter more, Myo-Reps could give similar or greater improvements despite less volume and shorter sessions.

Design: Parallel-group randomized trial in healthy adults, 1:1 allocation, stratified by gender and age, using a central web-based randomization system run by an independent trial unit; allocation was concealed until enrolment. All sessions were directly supervised, and load progression rules were identical in both groups. Week 1: familiarization and baseline body composition. Week 2: baseline strength testing. Weeks 3-11: training. Week 12: repeat testing.

Analysis: No sample-size calculation was performed (convenience sample). Strength comparisons are exploratory and analysed separately for each exercise.

Registration note: This record was registered retrospectively, after data collection was completed. Outcomes are described as defined in the manuscript submitted for publication.

02

Conditions studied

  • Resistance Exercise
  • Muscle Strength Development

Keywords

  • Myo-Reps
  • resistance training
  • strength training
  • rest-pause training
  • training volume
  • time efficiency
  • muscle strength
  • fat-free mass
03

In context

Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 495 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18-65 years
  • Generally good health
  • No medical for heavy resistance training

Exclusion criteria

Exclusion Criteria:

  • highly advanced trainees
  • pregnancy
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
34 participants (actual)

Study arms

  • Experimental
    Myo-Rep

    Nine weeks (weeks 3-11) of two supervised full-body sessions per week on 10 resistance-training machines. For each exercise: one activation set of 8-15 repetitions close to failure, followed by three mini-sets of 3-5 repetitions with the same load, separated by 10-20 seconds of rest. Load progression criteria were identical to the traditional training group.

    Other: Myo-Reps resistance training

  • Active comparator
    Traditional three-set training

    Nine weeks (weeks 3-11) of two supervised full-body sessions per week on the same 10 resistance-training machines. For each exercise: three sets of 8-15 repetitions separated by 1-3 minutes of rest. Load progression criteria were identical to the Myo-Reps group.

    Other: Traditional three-set resistance training

Interventions

  • OtherMyo-Reps resistance training

    Supervised full-body machine-based resistance training, twice weekly for nine weeks. Each exercise: one activation set of 8-15 repetitions close to failure, then three mini-sets of 3-5 repetitions with the same load and 10-20 seconds of rest between sets.

  • OtherTraditional three-set resistance training

    Supervised full-body machine-based resistance training, twice weekly for nine weeks, using the same 10 exercises. Each exercise: three sets of 8-15 repetitions with 1-3 minutes of rest between sets.

06

What researchers measure

Primary outcomes

  1. Change in exercise-specific muscular strength (estimated one-repetition maximum, e1RM) across 10 machine exercises

    e1RM was derived from 3-10 repetition-maximum tests (Epley equation) for each of the 10 trained machine exercises. Each exercise was analysed separately, and the between-group difference in change from baseline to post-intervention is the outcome.

    Time frame: Baseline (week 2) to post-intervention (week 12)

Secondary outcomes

  1. Change in fat-free mass

    Measured by bioelectrical impedance (InBody 770).

    Time frame: Baseline (week 1) to post-intervention (week 12)

  2. Session duration

    Time taken to complete a training session, averaged per participant.

    Time frame: Training weeks 3-11

  3. Weekly volume load

    Load × repetitions, summed across exercises and averaged per week.

    Time frame: Training weeks 3-11

  4. Repetitions close to failure

    Estimated number of repetitions performed close to muscular failure during training.

    Time frame: raining weeks 3-11

  5. Session rating of perceived exertion (session RPE)

    Participant-rated exertion for each training session.

    Time frame: Training weeks 3-11

07

Study locations

1 site
  • Sit Trening HelgasetrSit
    Trondheim, Trøndelag 7030, Norway
08

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data underlying the published results will be made available to qualified researchers on reasonable request to the corresponding author, after publication of the main article. Requests should include a brief research proposal.

Time frame: Data will be available beginning after publication of the main article and for at least 5 years thereafter.

Access criteria: De-identified individual participant data will be shared with qualified researchers on reasonable request to the corresponding author (Philip Meisterl, NTNU), who will review each request. Requesters should provide a short research proposal. Data are shared only for scientific research purposes, consistent with participants' consent and Norwegian data protection regulations (GDPR). Data will be sent securely by email or a secure file-transfer link.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07914361
Responsible party
Sponsor
First posted
Nov 3, 2026
Start date
Aug 26, 2025
Primary completion
Dec 3, 2025
Completion
Dec 3, 2025
Last update
Nov 3, 2026

Study contacts

Marius S Fimland, Phd
principal investigator · NTNU - Norwegian University of Science and Technology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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