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Muscular StrengthNCT07860151

The Effects of a 12-week Block Periodization vs. Daily Undulating Periodization on Muscular Strength and Cognitive Function in Healthy Young Adults.

A study testing Block Periodization Resistance Training and Daily Undulating Periodization Resistance Training in people with Muscular Strength, run by Gdansk University of Physical Education and Sport at 1 site in Poland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study compared the effects of two resistance training periodization models, block periodization and daily undulating periodization, on muscular strength and force production in healthy young adults with limited resistance training experience. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Muscular Strength
What is being tested?
Block Periodization Resistance Training and Daily Undulating Periodization Resistance Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
62 participants
Where
1 sitePoland
Study dates
4 Sep 2023to 26 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 0-2,5 years of strength training experience
  • between the ages of 18 and 35
  • without chronic diseases that would preclude resistance training

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • University of Physical Education and Sport

    Gdansk

Other trials in Poland

About this study

This study compared the effects of two resistance training periodization models, block periodization and daily undulating periodization, on muscular strength and force production in healthy young adults with limited resistance training experience. Participants were randomly assigned to a block periodization group, a daily undulating periodization group, or a non-training control group. The two training groups completed three supervised resistance training sessions per week for 12 weeks. Both training programs used the same exercises and were designed to have similar total training volume and average programmed relative intensity, but differed in how training volume and intensity were organized over time. Muscular strength and force production were assessed before and after the intervention using the isometric mid-thigh pull and single-joint isometric strength testing of the knee and elbow.

Read the detailed description

This was a randomized, controlled, parallel-group study designed to compare the effects of block periodization (BP) and daily undulating periodization (DUP) on maximal and rapid isometric force production in healthy young adults.

Participants were randomly assigned to one of three groups: block periodization, daily undulating periodization, or a non-training control group. The intervention lasted 12 weeks. Participants in both resistance training groups completed three supervised training sessions per week, for a total of 36 planned sessions.

The BP and DUP groups performed the same resistance exercises and were programmed to complete equivalent total training volume and similar average programmed relative intensity across the 12-week intervention. The principal difference between the groups was the temporal organization of training volume and intensity. In the BP group, training was organized into sequential three-week blocks emphasizing different loading characteristics. In the DUP group, loading variables were varied more frequently between training sessions within each weekly microcycle.

Before and after the 12-week intervention, participants completed assessments of muscular strength and force production. Maximal and rapid force production were assessed using the isometric mid-thigh pull (IMTP), including peak force and force produced at 150, 200, and 250 milliseconds after contraction onset. Single-joint isometric strength of the knee flexors and extensors and elbow flexors and extensors was assessed using a Biodex System 4 Pro dynamometer. Body mass and body composition were also assessed.

The purpose of the study was to determine whether differences in the organization of resistance training, when exercise selection, total training volume, and average programmed relative intensity were controlled, resulted in different adaptations in maximal and rapid force production.In addition, cognitive function was assessed at the beginning and end of the 12-week intervention using the Stroop test.

Being tested
Block Periodization Resistance Training, Daily Undulating Periodization Resistance Training

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Block Periodization Resistance TrainingBehavioural

    Also called BP

    Participants completed a 12-week supervised block periodization resistance training program with three sessions per week. Training was organized into four consecutive three-week blocks. The programmed relative intensities across the four blocks were approximately 70%, 83%, 78%, and 90% of estimated 1RM, respectively, with corresponding changes in sets and repetitions. Exercise selection, total programmed training volume, and average programmed relative intensity across the 12-week intervention were matched to the Daily Undulating Periodization group. Loads were individually adjusted based on performance and repetitions in reserve (RIR).

  • Daily Undulating Periodization Resistance TrainingBehavioural

    Also called DUP

    Participants completed a 12-week supervised daily undulating periodization resistance training program with three sessions per week. Training volume and relative intensity varied between sessions within each weekly microcycle, using loading conditions corresponding to approximately 70%, 78%, 83%, and 90% of estimated 1RM across the intervention. Exercise selection, total programmed training volume, and average programmed relative intensity across the 12-week intervention were matched to the Block Periodization group. Loads were individually adjusted based on performance and repetitions in reserve (RIR).

Study groups in NCT07860151
Study groupRoleWhat they receive
Block Periodization (BP)ExperimentalParticipants completed a 12-week supervised block-periodized resistance training program consisting of three training sessions per week. Training was organized into sequential three-week blocks with systematic changes in training volume and relative intensity. Exercise selection, total programmed training volume, and average programmed relative intensity across the intervention were matched to the Daily Undulating Periodization group.
Receives: Behavioral: Block Periodization Resistance Training
Daily Undulating Periodization (DUP)Active comparatorParticipants completed a 12-week supervised daily undulating resistance training program consisting of three training sessions per week. Training volume and relative intensity varied between training sessions within each weekly microcycle. Exercise selection, total programmed training volume, and average programmed relative intensity across the intervention were matched to the Block Periodization group.
Receives: Behavioral: Daily Undulating Periodization Resistance Training
Control (CON)No interventionParticipants did not participate in the resistance training intervention and were instructed to maintain their usual physical activity throughout the 12-week study period.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. maximal and rapid force production characteristics derived from the IMTP, including net peak force and force expressed at 150-, 200-, and 250 ms

    Measured: At the start and end of the 12-week intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2026
  2. Study start4 Sep 2023
  3. Primary completion2 Jun 2024
  4. Study completion26 Jun 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
62 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07860151
Sponsor's protocol ID
AWFiS/2025_2_MK
Status last verified
Oct 2026
First submitted
28 Sep 2026
Last updated
6 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Block Periodization Resistance Training and Daily Undulating Periodization Resistance Training in people with Muscular Strength, run by Gdansk University of Physical Education and Sport at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

maximal and rapid force production characteristics derived from the IMTP, including net peak force and force expressed at 150-, 200-, and 250 ms (time frame: At the start and end of the 12-week intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2026.

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