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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.

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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

62

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Gdansk, Polen
        • University of Physical Education and Sport

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 35 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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).

Andre navn:
  • BP
Aktiv 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).

Andre navn:
  • DUP
Ingen inngripen: 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.

Hva måler studien?

Primære resultatmål

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

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Omega-3 assessments
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

4. september 2023

Primær fullføring (Faktiske)

2. juni 2024

Studiet fullført (Faktiske)

26. juni 2024

Datoer for studieregistrering

Først innsendt

28. september 2026

Først innsendt som oppfylte QC-kriteriene

2. oktober 2026

Først lagt ut (Faktiske)

6. oktober 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

2. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • AWFiS/2025_2_MK

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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