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Individualized Versus Non-Individualized Resistance Training

5. November 2026 aktualisiert von: Christophe Delecluse, Universitaire Ziekenhuizen KU Leuven

Eine maßgeschneiderte Intervention zur Vorbeugung altersbedingter Rückgänge der Muskelkraft und Funktionsfähigkeit

Preserving functional ability is crucial for healthy aging. Unfortunately, age-related decreases in muscle power often lead to declines in functional ability. As power is the product of force and velocity, decreases in power can originate from changes in muscle force, contraction velocity, or both, varying between individuals. The primary method to prevent functional disability is power-based resistance training. Although training interventions are effective for most older adults, they do not induce substantial improvements in a subset of the population. These inconsistent outcomes may arise from neglecting the observed differences in the force-velocity (F-V) profiles between individuals. Therefore, this study provides a novel approach to resistance exercise, in which exercise dose is tailored according to the individual's F-V profile. The effectiveness of the tailored method will be assessed in a randomized control trial, comparing the effects of an individualized and a non-individualized 12-week training intervention on muscle power parameters and functional ability.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Tatsächlich)

80

Phase

  • Unzutreffend

Kontakte und Standorte

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

Studienorte

    • Vlaams-Brabant
      • Leuven, Vlaams-Brabant, Belgien, 3000
        • KU Leuven - Department of Movement Sciences

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

65 Jahre und älter (Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Community-dwelling adults
  • At least 65 years old

Exclusion Criteria:

  • Systematic engagement in resistance exercise during the past year
  • Unstable cardiovascular disease, neuromuscular disease, acute infection or fever
  • Recent surgery
  • Lower-extremity injuries
  • Low levels of functional ability (i.e., SPPB score ≤ 9)
  • Cognitive malfunctioning (i.e., Mini-Mental State Examination < 24)

Studienplan

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

Wie ist die Studie aufgebaut?

Designdetails

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

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Individualized resistance exercise program

Individualized exercise dose. All individuals perform resistance exercises at a load that targets their deficit. Individuals with a velocity deficit train at low loads while individuals with a force deficit train at high loads.

2x/week, 35-45 min sessions, on leg press machine

Aktiver Komparator: Non-individualized resistance exercise program

Non-individualized exercise dose. All individuals perform resistance exercises at a load that does not target their deficit. Individuals with a velocity deficit train at high loads while individuals with a force deficit train at low loads.

2x/week, 35-45 min sessions, on leg press machine

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Maximal power (Pmax)
Zeitfenster: Change from baseline at 6 and 12 weeks

Participants performed explosive unilateral leg extensions with the dominant leg at five submaximal loads on a pneumatic leg press (Leg Press Air 400, Keiser, USA). Submaximal loads were scaled to the estimated maximal isometric force derived from the familiarization session. The three lighter loads were performed three times each and the two heavier loads twice, with the repetition yielding the highest mean concentric velocity retained for analysis. Participants subsequently performed single repetitions at incrementally increasing loads until 1-RM was reached. Rest intervals were adjusted according to the load of the preceding trial: 60 s after the three lightest loads, 90 s after the two heavier loads, and 120 s during the incremental trials leading to 1-RM. For each load, the mean concentric velocity of the best trial was used to establish the individual force-velocity (F-V) relationship using linear regression, from which the maximal power (Pmax; W) was estimated.

Change from baseline at 6 and 12 weeks
Maximal isometric force (F0)
Zeitfenster: Change from baseline at 6 and 12 weeks

Participants performed explosive unilateral leg extensions with the dominant leg at five submaximal loads on a pneumatic leg press (Leg Press Air 400, Keiser, USA). Submaximal loads were scaled to the estimated maximal isometric force derived from the familiarization session. The three lighter loads were performed three times each and the two heavier loads twice, with the repetition yielding the highest mean concentric velocity retained for analysis. Participants subsequently performed single repetitions at incrementally increasing loads until 1-RM was reached. Rest intervals were adjusted according to the load of the preceding trial: 60 s after the three lightest loads, 90 s after the two heavier loads, and 120 s during the incremental trials leading to 1-RM. For each load, the mean concentric velocity of the best trial was used to establish the individual force-velocity (F-V) relationship using linear regression, from which maximal isometric force (F0; N) was estimated.

Change from baseline at 6 and 12 weeks
Maximal unloaded velocity (V0)
Zeitfenster: Change from baseline at 6 and 12 weeks

Participants performed explosive unilateral leg extensions with the dominant leg at five submaximal loads on a pneumatic leg press (Leg Press Air 400, Keiser, USA). Submaximal loads were scaled to the estimated maximal isometric force derived from the familiarization session. The three lighter loads were performed three times each and the two heavier loads twice, with the repetition yielding the highest mean concentric velocity retained for analysis. Participants subsequently performed single repetitions at incrementally increasing loads until 1-RM was reached. Rest intervals were adjusted according to the load of the preceding trial: 60 s after the three lightest loads, 90 s after the two heavier loads, and 120 s during the incremental trials leading to 1-RM. For each load, the mean concentric velocity of the best trial was used to establish the individual force-velocity (F-V) relationship using linear regression, from which maximal unloaded velocity (V0; m/s) was estimated.

Change from baseline at 6 and 12 weeks
Force-velocity slope
Zeitfenster: Change from baseline at 6 and 12 weeks

Participants performed explosive unilateral leg extensions with the dominant leg at five submaximal loads on a pneumatic leg press (Leg Press Air 400, Keiser, USA). Submaximal loads were scaled to the estimated maximal isometric force derived from the familiarization session. The three lighter loads were performed three times each and the two heavier loads twice, with the repetition yielding the highest mean concentric velocity retained for analysis. Participants subsequently performed single repetitions at incrementally increasing loads until 1-RM was reached. Rest intervals were adjusted according to the load of the preceding trial: 60 s after the three lightest loads, 90 s after the two heavier loads, and 120 s during the incremental trials leading to 1-RM. For each load, the mean concentric velocity of the best trial was used to establish the individual force-velocity (F-V) relationship using linear regression, from which the F-V slope (Ns/m) was derived.

Change from baseline at 6 and 12 weeks

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Short Physical Performance Battery (SPPB)
Zeitfenster: Score at baseline

Total score on the SPPB (min 0, max 12, higher scores indicate better performance)

Score at baseline
Hand grip strength
Zeitfenster: Change from baseline at 6 and 12 weeks

Maximal grip strength (kg) of the dominant hand using an isometric dynamometer adjusted for hand size

Change from baseline at 6 and 12 weeks
Maximal gait speed
Zeitfenster: Change from baseline at 6 and 12 weeks

The average time (s) to walk 10m as fast as possible

Change from baseline at 6 and 12 weeks
Countermovement jump
Zeitfenster: Change from baseline at 6 and 12 weeks

The jump height (mm) in a countermovement jump

Change from baseline at 6 and 12 weeks
Timed up-and-go
Zeitfenster: Change from baseline at 6 and 12 weeks

The time (s) needed to stand up from a chair, walk 3 m, turn, walk back and sit down again as fast as possible

Change from baseline at 6 and 12 weeks
5-repetition sit-to-stand time
Zeitfenster: Change from baseline at 6 and 12 weeks

The time (s) needed to complete the 5-repetition sit-to-stand test

Change from baseline at 6 and 12 weeks
5-repetition sit-to-stand power
Zeitfenster: Change from baseline at 6 and 12 weeks

The average power (watt) produced during the 5-repetition sit-to-stand test

Change from baseline at 6 and 12 weeks
30-second sit-to-stand repetitions
Zeitfenster: Change from baseline at 6 and 12 weeks

The number of repetitions completed during the 30-second sit-to-stand test

Change from baseline at 6 and 12 weeks
30-second sit-to-stand power
Zeitfenster: Change from baseline at 6 and 12 weeks

The average power (watt) produced during the 30-second sit-to-stand test

Change from baseline at 6 and 12 weeks
Stair ascent time
Zeitfenster: Change from baseline at 6 and 12 weeks

The time (s) needed to ascend a flight of stairs

Change from baseline at 6 and 12 weeks
Stair ascent power
Zeitfenster: Change from baseline at 6 and 12 weeks

The average power (Watt) produced during the stair ascent test

Change from baseline at 6 and 12 weeks
Exercise adherence
Zeitfenster: Total adherence over 12-week period

Number of sessions attended as a percentage of total sessions planned

Total adherence over 12-week period
Absolute training load
Zeitfenster: Consistently recorded throughout the 12-week intervention

The absolute load (kg) used during training sessions

Consistently recorded throughout the 12-week intervention
Relative training load
Zeitfenster: Consistently recorded throughout the 12-week intervention

The relative load (%1RM) used during training sessions

Consistently recorded throughout the 12-week intervention
Number of repetitions
Zeitfenster: Consistently recorded throughout the 12-week intervention

The number of repetitions (n) completed per set

Consistently recorded throughout the 12-week intervention
Highest movement velocity within a set
Zeitfenster: Consistently recorded throughout the 12-week intervention

The velocity (m/s) of the fastest repetition in a set (Vmax)

Consistently recorded throughout the 12-week intervention
Lowest movement velocity within a set
Zeitfenster: Consistently recorded throughout the 12-week intervention

The velocity (m/s) of the slowest repetition in a set (Vmin)

Consistently recorded throughout the 12-week intervention
Velocity loss
Zeitfenster: Consistently recorded throughout the 12-week intervention

The percentage difference between the highest and lowest movement velocity in a set = ([Vmax - Vmin] / Vmax) × 100

Consistently recorded throughout the 12-week intervention
Set-volume index
Zeitfenster: Consistently recorded throughout the 12-week intervention

The number of repetitions × relative load (%1-RM) per set

Consistently recorded throughout the 12-week intervention
Session-volume index
Zeitfenster: Consistently recorded throughout the 12-week intervention

The sum of set volumes per session

Consistently recorded throughout the 12-week intervention

Mitarbeiter und Ermittler

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

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

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)

20. Mai 2024

Primärer Abschluss (Tatsächlich)

4. Dezember 2025

Studienabschluss (Tatsächlich)

4. Dezember 2025

Studienanmeldedaten

Zuerst eingereicht

5. März 2024

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. Juni 2024

Zuerst gepostet (Tatsächlich)

10. Juni 2024

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • S68434

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

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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