ClinicalTrials.gg
CompletedNCT07905690BICEPS-PTUpdated Oct 29, 2026

Adaptations in the Biceps Brachii Muscles to Different Modalities of Resistance Training

An interventional study of Strength training in Exercise Training, sponsored by Umeå University. Completed. Open to male participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Umeå University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 22 years 1 month after the study started (first participant enrolled Sep 2004, registered Oct 2026).
Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

This study examined how two types of resistance training affect the biceps muscle over six weeks in healthy young men. Participants performed either low-repetition, heavy-load training designed to improve maximal strength or high-repetition training designed to improve muscular endurance. Training was supervised and performed twice weekly.

Researchers measured arm strength and muscular endurance before and after training. They also collected small samples of biceps muscle tissue to examine muscle-fibre characteristics and changes in muscle proteins. These protein measurements were intended to identify early changes in muscle that may occur before visible changes in muscle size or measurable improvements in performance.

The study found no clear differences between the two training approaches in strength, endurance, muscle-fibre size, or muscle-fibre type after six weeks. However, the two programs were associated with different patterns of change in muscle proteins. These findings may help researchers understand the early biological processes through which different types of resistance exercise affect skeletal muscle. This was a small exploratory study, so the results may not apply to other populations or longer training programs.

Read the detailed description

This randomized pilot study examined early changes in the biceps brachii muscle after two different resistance-training programs. The study was conducted in Umeå, Sweden, between January and December 2005. Its purpose was to compare changes in muscle strength, muscular endurance, muscle-fibre characteristics, blood markers, and muscle proteins after six weeks of either heavy, low-repetition resistance training or high-repetition resistance training.

Ten healthy male university students, aged 18 to 40 years and recreationally resistance trained, provided written informed consent and were randomly assigned to one of two groups. Five participants performed maximal-strength training and five performed endurance-oriented strength training. The random sequence was computer-generated by a researcher not involved in outcome assessment. Participants and instructors knew the assigned program, but laboratory staff and data analysts were blinded to group assignment.

Both groups trained their biceps muscles twice weekly for six weeks under individual supervision. Training consisted of bilateral preacher curls with free weights. The maximal-strength group performed five sets of three repetitions using a weight that could be lifted for three repetitions, with four minutes of rest between sets. The endurance-oriented group performed three sets of 30 repetitions using a weight that could be lifted for 30 repetitions, also with four minutes of rest. Training loads were adjusted as participants' strength changed.

Before and after the training period, participants completed tests of right-arm biceps strength and endurance using an isokinetic dynamometer. The study measured peak elbow-flexion force, total work during repeated contractions, and fatigue during the endurance test. Blood samples were collected before and after training to measure selected hormones and creatine kinase. Muscle-biopsy samples were collected before training from the left biceps and after training from the right biceps, using local anaesthesia. The samples were examined for muscle-fibre type and size and for changes in muscle proteins using proteomic methods.

The study was exploratory and included a small number of participants. No intervention-related adverse events were reported. One participant developed a small raised scar after a muscle biopsy. The findings were intended to help identify early molecular changes in muscle that may occur before measurable changes in strength, endurance, or muscle size.

02

Conditions studied

  • Exercise Training

Browse trials for

Keywords

  • muslce
  • proteomics
  • exercise
03

In context

Motor Activity

2,684 studies on the registry are indexed under Motor Activity; 1,217 are open to participants now.

This study's enrollment of 10 is below the median of 60 across 2,344 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Umeå University is the lead sponsor of 272 studies on the registry; 60 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
No

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

  • Male.
  • Aged 18 to 40 years.
  • Healthy.
  • Recreationally resistance trained.
  • Able and willing to provide informed consent and complete the six-week supervised resistance-training program, strength testing, blood sampling, and muscle-biopsy procedures.

Exclusion criteria

Exclusion Criteria:

  • Female sex.
  • Younger than 18 years or older than 40 years.
  • Not recreationally resistance trained.
  • Unable or unwilling to provide informed consent or complete the study procedures.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
10 participants (actual)

Study arms

  • Experimental
    Maximal-Strength Training (MaxST)

    A supervised, isolated biceps-brachii resistance-training intervention delivered twice weekly for six weeks. Participants performed bilateral preacher curls (Scott curls) with free weights on an EZ bar, using a standardized range of motion from full elbow extension to 135 degrees of elbow flexion. Each session comprised five sets of three-repetition maximum (3RM) with four minutes of rest between sets. The concentric phase was performed at maximal intended speed, while the eccentric phase was controlled over approximately three seconds. The load was individually progressed as the participant's 3RM improved. This intervention differs from the endurance-oriented arm primarily in its low-repetition, high-load prescription

    Behavioral: Strength training

  • Experimental
    Endurance-Oriented Strength Training (EndST)

    A supervised, isolated biceps-brachii resistance-training intervention delivered twice weekly for six weeks. Participants performed bilateral preacher curls (Scott curls) with free weights on an EZ bar, using the same standardized range of motion from full elbow extension to 135 degrees of elbow flexion. Each session comprised three sets of 30-repetition maximum (30RM) with four minutes of rest between sets. The concentric phase was performed at maximal intended speed, while the eccentric phase was controlled over approximately three seconds. The load was individually progressed as the participant's 30RM improved. This intervention differs from the maximal-strength arm primarily in its high-repetition, lower-load prescription.

    Behavioral: Strength training

Interventions

  • BehavioralStrength training

    A supervised, isolated biceps-brachii resistance-training intervention delivered twice weekly for six weeks. Participants performed bilateral preacher curls (Scott curls) with free weights on an EZ bar, using a standardized range of motion from full elbow extension to 135 degrees of elbow flexion.

06

What researchers measure

Primary outcomes

  1. Change in biceps brachii muscle protein profile

    Muscle-protein abundance was assessed in biceps brachii biopsy samples collected before and after the training intervention. Intact proteins were separated and quantified using two-dimensional difference gel electrophoresis (2D-DIGE). Protein spots with changed abundance were selected for identification by mass spectrometry. The outcome was the within-group change in abundance of individual protein spots from baseline to after training, compared between the maximal-strength and endurance-oriented strength-training groups.

    Time frame: Baseline and immediately after the 6-week resistance-training intervention (approximately Day 45).

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Hammert WB, Yamada Y, Kataoka R, Song JS, Spitz RW, Wong V, Seffrin A, Loenneke JP. Changes in Absolute and Relative Muscular Endurance After Resistance Training: A Review of the Literature With Considerations for Future Research. J Strength Cond Res. 2025 Apr 1;39(4):474-491. doi: 10.1519/JSC.0000000000005084. PubMed 40153563 ↗

Individual participant data

Plan to share: No

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Sep 2004 to primary completion in Jan 2014, 112 months.

Of 1,755 non-industry interventional studies with no phase under Motor Activity, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 46. This study's 112 months is above that.

Counting every sponsor, half of 1,767 studies reached it within 23 months; a quarter within 9 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 23, 2026
First posted
Oct 29, 2026
StartActual
Sep 1, 2004
Primary completionActual
Jan 23, 2014
CompletionActual
Jun 29, 2026
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 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
NCT07905690
Lead sponsor
Umeå University
Responsible party
Sponsor
First posted
Oct 29, 2026
Start date
Sep 1, 2004
Primary completion
Jan 23, 2014
Completion
Jun 29, 2026
Last update
Oct 29, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion