High-Intensity Functional Training (HIFT) vs Moderate-Intensity Continuous Training (MICT) in College Students
29 de julho de 2026 atualizado por: Arlette Perry, University of Miami
The Effects of Interval Compared to Continuous Training on Physical Variables and Vascular Health in College Students: A Three-Arm Randomized Controlled Trial
The purpose of this study is to compare two types of exercise programs in college students: high-intensity functional training and moderate-intensity continuous training.
The study evaluates whether these exercise programs improve body composition, physical fitness, and blood vessel health compared with a group that does not participate in exercise training.
In addition, the study examines whether changes in body composition and physical fitness are associated with changes in blood vessel health.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Tipo de estudo
Intervencional
Inscrição (Estimado)
90
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
- Nome: Arlette Perry, PhD
- Número de telefone: 305-284-3025
- E-mail: aperry@miami.edu
Locais de estudo
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Florida
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Coral Gables, Florida, Estados Unidos, 33146
- Merrick Building, University of Miami
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Contato:
- Arlette Perry, PhD
- Número de telefone: 305-284-3025
- E-mail: aperry@miami.edu
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-
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
- Adulto
Aceita Voluntários Saudáveis
Sim
Descrição
Inclusion Criteria:
- Age 18 to 35 years.
- Currently enrolled college or university student.
- Able to provide written informed consent.
- Able to attend baseline and post-intervention testing visits and participate in assigned intervention sessions.
- Cleared for exercise participation based on the health screening form and investigator review.
Exclusion Criteria:
- Known cardiovascular, metabolic, pulmonary, renal, neurological, musculoskeletal, or endocrine disorder that would make exercise unsafe or confound outcome measures.
- Current pregnancy or planning pregnancy during the study period.
- Current smoking, vaping nicotine products, or use of tobacco products.
- Uncontrolled hypertension or resting blood pressure values that make exercise testing unsafe based on investigator judgment.
- Use of medications known to substantially affect cardiovascular function, vascular tone, or exercise responses, unless approved by the PI.
- Any injury, orthopedic limitation, or medical condition preventing safe participation in HIFT, MICT, or physical fitness testing.
- Currently participating in structured high-intensity interval, functional, or endurance training more than two days per week during the previous three months.
- Do not speak English.
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: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: High-intensity Functional Training (HIFT) Group
Participants in this group will perform supervised high-intensity functional training (HIFT) using multi-joint functional movements.
Participants will complete training 3 days per week for 8 weeks.
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Participants will perform supervised high-intensity functional training using multi-joint functional movements that may include body-weight exercises, resistance-based movements, step-ups, squats, lunges, push-ups or modified push-ups, core exercises, etc.
The intervention will be conducted over 8 weeks, with participants completing three sessions per week.
Each session will last approximately 40 to 60 minutes.
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Experimental: Moderate-intensity Continuous Training (MICT) Group
Participants in this group will perform supervised moderate-intensity continuous aerobic exercise.
Participants will complete training 3 days per week for 8 weeks.
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Participants will perform supervised moderate-intensity continuous aerobic exercise such as treadmill walking/jogging, cycling, elliptical exercise, or step-based aerobic activity.
The intervention will be conducted over 8 weeks, with participants completing three sessions per week.
Each session will last approximately 40 to 60 minutes.
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Sem intervenção: Control Group
The control group will not receive supervised exercise training during the intervention period.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Carotid-Femoral Pulse Wave Velocity (cfPWV)
Prazo: Baseline and Week 10 (post-intervention)
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Carotid-femoral pulse wave velocity (cfPWV) will be measured in meters per second (m/s) at baseline and post intervention as an indicator of arterial stiffness.
Measurement will be obtained using the SphygmoCor XCEL device (AtCor Medical) with upper arm and thigh cuffs with carotid artery applanation tonometry to assess pulse wave transit time
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Baseline and Week 10 (post-intervention)
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Change in Central Augmentation Index (cAIx)
Prazo: Baseline and Week 10 (post-intervention)
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The central augmentation index (cAIx), expressed as a percentage, will be assessed at baseline and post-intervention using the SphygmoCor XCEL device via pulse wave analysis of the central arterial waveform derived from carotid artery tonometry and peripheral blood pressure measurements.
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Baseline and Week 10 (post-intervention)
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Change in Mean Arterial Pressure (MAP)
Prazo: Baseline and Week 10 (post-intervention)
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Mean arterial pressure (MAP), measured in millimeters of mercury (mmHg), will be assessed at baseline and post-intervention.
MAP will be assessed using the SphygmoCor XCEL system (AtCor Medical) based on an algorithm derived from peripheral blood pressure obtained via an automated upper arm cuff.
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Baseline and Week 10 (post-intervention)
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Percent Change in Flow-Mediated Dilation (FMD)
Prazo: Baseline and Week 10 (post-intervention)
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Flow-Mediated Dilation (FMD) will be measured at baseline and post-intervention using a Philips Affiniti 50 ultrasound system and expressed as the percent (%) change in brachial artery diameter from pre-occlusion baseline to peak dilation following a 5-minute forearm occlusion.
The outcome will be reported as the change in FMD (%) from baseline to post-intervention.
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Baseline and Week 10 (post-intervention)
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Change in Carotid Intima-Media Thickness (cIMT)
Prazo: Baseline and Week 10 (post-intervention)
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Carotid intima-media thickness (cIMT), measured in millimeters (mm), will be assessed using a Philips Affiniti 50 ultrasound system at baseline and post-intervention.
High-resolution B-mode images of the distal common carotid artery will be acquired, and mean wall thickness will be calculated from standardized image segments of the left and right carotid arteries.
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Baseline and Week 10 (post-intervention)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Body mass index (BMI)
Prazo: Baseline and Week 10 (post-intervention)
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Body mass index (BMI), measured in kilograms per meter squared (kg/m²), will be calculated from standardized measurements of height and weight.
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Baseline and Week 10 (post-intervention)
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Change in Waist Circumference (WC)
Prazo: Baseline and 10 weeks (post-intervention)
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Waist circumference (WC), measured in centimeters (cm), will be assessed using a standardized measuring tape at the level of the iliac crest.
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Baseline and 10 weeks (post-intervention)
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Change in Body fat percentage (BF%)
Prazo: Baseline and 10 weeks (post-intervention)
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Body fat percentage (BF%) will be assessed using the SECA mBCA (Medical Body Composition Analyzer) bioelectrical impedance analyzer and reported as a percentage (%).
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Baseline and 10 weeks (post-intervention)
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Change in Skeletal Muscle Mass (SMM)
Prazo: Baseline and 10 weeks (post-intervention)
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Skeletal muscle mass (SMM) will be assessed using the SECA mBCA (Medical Body Composition Analyzer) bioelectrical impedance analyzer and reported in kilograms (kg).
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Baseline and 10 weeks (post-intervention)
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Change in visceral adipose tissue (VAT)
Prazo: Baseline and 10 weeks (post-intervention)
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Visceral adipose tissue (VAT) will be measured using the SECA mBCA (Medical Body Composition Analyzer) bioelectrical impedance analyzer and reported in liters (L).
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Baseline and 10 weeks (post-intervention)
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Change in Muscular Strength
Prazo: Baseline and Week 10 (post-intervention)
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Muscular strength will be measured to include lower body muscular strength and upper body handgrip strength.
Lower body muscular strength will be assessed using a hip-hinge/deadlift-style test with a force plate transducer to measure maximal force production.
Upper body handgrip strength will be assessed using a calibrated hydraulic hand dynamometer.
Results will be reported in kilograms (kg).
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Baseline and Week 10 (post-intervention)
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Change in Cardiorespiratory Fitness
Prazo: Baseline and Week 10 (post-intervention)
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Cardiorespiratory fitness will be assessed using the Queens College Step Test.
Heart rate will be recorded at the end of the test and used to measure cardiorespiratory fitness in milliliters of oxygen consumed per kilogram of body weight per minute (mL / kg / min).
The outcome will be reported as the change from baseline to post-intervention.
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Baseline and Week 10 (post-intervention)
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Change in Muscular Endurance
Prazo: Baseline and Week 10 (post-intervention)
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Muscular endurance will be assessed using the 1-minute curl-up test.
Participants will complete as many correctly performed curl-ups as possible within 1 minute, and the number of valid repetitions will be recorded.
The outcome will be reported as the change from baseline to post-intervention.
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Baseline and Week 10 (post-intervention)
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Change in Flexibility (Sit-and-Reach test)
Prazo: Baseline and Week 10 (post-intervention)
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Flexibility will be assessed using the Sit-and-Reach test.
Participants will reach forward while seated with legs extended, and the maximum distance reached beyond the toes will be recorded in centimeters (cm).
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Baseline and Week 10 (post-intervention)
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Change in Flexibility (Trunk Lift test)
Prazo: Baseline and Week 10 (post-intervention)
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Flexibility will be assessed using the Trunk Lift Test.
Participants will lie prone and lift their upper body off the floor while maintaining a neutral head position.
The vertical distance from the floor to the participant's chin will be measured in centimeters (cm).
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Baseline and Week 10 (post-intervention)
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Arlette Perry, PhD, University of Miami
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 (Estimado)
1 de setembro de 2026
Conclusão Primária (Estimado)
1 de junho de 2028
Conclusão do estudo (Estimado)
1 de junho de 2028
Datas de inscrição no estudo
Enviado pela primeira vez
15 de julho de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
29 de julho de 2026
Primeira postagem (Real)
4 de agosto de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
4 de agosto de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
29 de julho de 2026
Última verificação
1 de junho de 2026
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 20260670
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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