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Acute Blood Flow Restriction Walking on Immune Cell Phenotype and Function

3 de novembro de 2026 atualizado por: Jonathan Little, University of British Columbia

Impact of Acute Blood Flow Restriction Walking on Immune Cell Phenotype and Function in Adults withT2D

To conduct a randomized control trial to determine the impact of acute blood flow restriction treadmill walking on immune cell counts, function, and phenotype in adults living with type 2 diabetes.

Visão geral do estudo

Status

Recrutamento

Condições

Descrição detalhada

Participants will be randomized to a regular treadmill walking condition or treadmill walking with blood flow restriction (BFR) condition. In both groups participants will complete 32 minutes of treadmill walking at a speed and grade that elicit 40-50% heart rate reserve. In the BFR group the cuffs will be inflated based on each participants individualized limb occlusion pressure (LOP). The cuffs will remain inflated for the entire session but will deflate for 1 minute every 10 minutes based on safety recommendations. The percentage of LOP will 60%. Blood samples will be obtained pre-exercise (PRE), during the final 2 minutes of the final occlusion cycle (OCC), and 3 minutes into the recovery period post-exercise (POST) to measure outcomes.

Tipo de estudo

Intervencional

Inscrição (Estimado)

20

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.

Contato de estudo

Locais de estudo

    • British Columbia
      • Kelowna, British Columbia, Canadá, V1V 1V7
        • Recrutamento
        • University of British Columbia Okanagan
        • Contato:

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

19 anos a 64 anos (Adulto)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Aged 19-64 years
  • Diagnosed with type 2 diabetes with current HbA1c 5.7-9.0%
  • Completing <150 minutes of moderate-vigorous physical activity per week.

Exclusion Criteria:

  • Chronic musculoskeletal condition or recent (within 2 years) cardiovascular event preventing participation in exercise.
  • Unstable type 2 diabetes medication of the last 3 months
  • Absolute contraindications to BFR (i.e., peripheral vascular disease)
  • A self-reported diagnosis of low iron concentrations, anemia, or being treated for these conditions
  • A diagnosis of any red blood cell-altering condition (i.e., sickle cell anemia, poikilocytosis)
  • Currently living with any cardiovascular disease, which would impact the ability to participate in exercise safely
  • Currently prescribed any medication which would impact the ability to use a heart rate monitor to accurately track intensity

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: Ciência básica
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Treadmill walking with blood flow restriction

Treadmill walking with blood flow restriction.

Participants will complete 32 minutes of treadmill walking at a speed and grade that elicit 40-50% heart rate reserve. The cuffs will be inflated based on each participants individualized limb occlusion pressure (LOP). The cuffs will remain inflated for the entire session but will deflate for 1 minute every 10 minutes based on safety recommendations. The percentage of LOP will 60%.

Comparador Ativo: Treadmill Walking

Treadmill walking.

Participants will complete 32 minutes of treadmill walking at a speed and grade that elicit 40-50% heart rate reserve.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in white blood cell count before, during, and after exercise.
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The white blood cell count will be measured using a hematology analyzer before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in monocyte count before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The monocyte count will be measured using a hematology analyzer before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in neutrophil count before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The neutrophil count will be measured using a hematology analyzer before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in eosinophil count before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The eosinophil count will be measured using a hematology analyzer before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in CD66b+ expression before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The CD66b+ expression will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in CD11b+ expression before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The CD11b+ expression will be measured using flow cytometer before, during, and after exercise

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in CD63+ expression before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The CD63+ expression will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in % of classical monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The % of classical monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in % of intermediate monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The % of intermediate monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in % of non-classical monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The % of non-classical monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in TLR-4 expression on classical monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The TLR-4 expression on classical monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in TLR-4 expression on intermediate monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The TLR-4 expression on intermediate monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in TLR-4 expression on non-classical monocytes before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The TLR-4 expression on non-classical monocytes will be measured using flow cytometry before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in plasma IL-6 before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The plasma IL-6 concentration will be measured using a multiplex assay before, during, and after exercise

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in plasma IL-10 before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The plasma IL-10 concentration will be measured using a multiplex assay before, during, and after exercise.

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in plasma TNF-α before, during, and after exercise
Prazo: Pre-exercise, during 32 minute of exercise, immediately post-exercise

The plasma TNF-α concentration will be measured using a multiplex assay before, during, and after exercise

Pre-exercise, during 32 minute of exercise, immediately post-exercise
Change in 4-h LPS-induced TNF-α before and after exercise
Prazo: Pre-exercise, immediately post-exercise

The LPS-induced TNF-α concentration will be measured from whole-blood culture supernatant using an ELISA before and after exercise.

Pre-exercise, immediately post-exercise
Change in 4-h LPS+IL10-induced TNF-α before and after exercise
Prazo: Pre-exercise, immediately post-exercise

The LPS+IL10-induced TNF-α concentration will be measured from whole-blood culture supernatant using an ELISA before and after exercise.

Pre-exercise, immediately post-exercise

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

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)

11 de fevereiro de 2026

Conclusão Primária (Estimado)

31 de dezembro de 2027

Conclusão do estudo (Estimado)

31 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

23 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

3 de novembro de 2026

Primeira postagem (Real)

10 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

10 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

3 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

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

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