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

2. Oktober 2026 aktualisiert von: Gdansk University of Physical Education and Sport

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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

62

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Gdansk, Polen
        • University of Physical Education and Sport

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 35 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria for the training group:

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Sonstiges
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Block Periodization (BP)

Participants 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.

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).

Andere Namen:
  • BP
Aktiver Komparator: Daily Undulating Periodization (DUP)

Participants 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.

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).

Andere Namen:
  • DUP
Kein Eingriff: Control (CON)

Participants did not participate in the resistance training intervention and were instructed to maintain their usual physical activity throughout the 12-week study period.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
maximal and rapid force production characteristics derived from the IMTP, including net peak force and force expressed at 150-, 200-, and 250 ms
Zeitfenster: At the start and end of the 12-week intervention
At the start and end of the 12-week intervention

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Omega-3 assessments
Zeitfenster: At the beginning and at the end of the 12-week training period

Assessment of fatty acids: EPA, DHA; omega-3 index, AA/EPA, omega-6: omega-3 in erythrocytes of participants.

At the beginning and at the end of the 12-week training period

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

4. September 2023

Primärer Abschluss (Tatsächlich)

2. Juni 2024

Studienabschluss (Tatsächlich)

26. Juni 2024

Studienanmeldedaten

Zuerst eingereicht

28. September 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. Oktober 2026

Zuerst gepostet (Tatsächlich)

6. Oktober 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. Oktober 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. Oktober 2026

Zuletzt verifiziert

1. Oktober 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • AWFiS/2025_2_MK

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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