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Individualized Versus Non-Individualized Resistance Training

5 de novembro de 2026 atualizado por: Christophe Delecluse, Universitaire Ziekenhuizen KU Leuven

Uma intervenção personalizada para prevenir declínios relacionados à idade na potência muscular e na capacidade funcional

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.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

80

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

65 anos e mais velhos (Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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)

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
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

Comparador Ativo: 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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Maximal power (Pmax)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Short Physical Performance Battery (SPPB)
Prazo: Score at baseline

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

Score at baseline
Hand grip strength
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: Consistently recorded throughout the 12-week intervention

The sum of set volumes per session

Consistently recorded throughout the 12-week intervention

Colaboradores e Investigadores

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Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

20 de maio de 2024

Conclusão Primária (Real)

4 de dezembro de 2025

Conclusão do estudo (Real)

4 de dezembro de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

5 de março de 2024

Enviado pela primeira vez que atendeu aos critérios de CQ

5 de junho de 2024

Primeira postagem (Real)

10 de junho de 2024

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

5 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • S68434

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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