- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07495410
Anderson-Fabry Disease Fitness Improvement Training (A-FAD-FIT)
Anderson-Fabry Disease Fitness Improvement Training: A-FAD-FIT
This study will evaluate physical function, cardiorespiratory fitness, muscle strength, and quality of life in patients with Fabry disease and assess the effects of a 12-week physiotherapy-led exercise programme. Participants will be non-randomly assigned to an exercise intervention group or a control group receiving no study-specific exercise intervention. The intervention group will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline. The control group will be assessed at baseline and 12 months after baseline.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Fabry disease is a rare X-linked lysosomal storage disorder associated with multisystem involvement, reduced exercise tolerance, fatigue, pain, and impaired quality of life. Evidence regarding structured physiotherapy and exercise interventions in this population remains limited.
The aim of this study is to evaluate functional and cardiorespiratory capacity in patients with Fabry disease and to investigate the effects of a 12-week physiotherapy-led exercise programme. Participants will be non-randomly assigned to either an exercise intervention group or a control group receiving no study-specific exercise intervention. Group assignment will primarily reflect participants' willingness to participate in the exercise programme and logistical feasibility, particularly the ability to attend regular supervised exercise sessions.
Participants in the intervention group will complete a 12-week physiotherapy-led programme consisting of one supervised exercise session per week and two home-based exercise sessions per week. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. The programme also includes a progressive increase in daily ambulatory physical activity, monitored primarily by daily step count. Participants in the intervention group will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline.
Participants in the control group will receive no study-specific exercise intervention and will be assessed at baseline and 12 months after baseline. The study will evaluate short-term changes following the exercise intervention as well as longer-term changes in the main study outcomes.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Jan Vávra, Masters
- Número de telefone: +420601200272
- E-mail: Jan.Vavra2@vfn.cz
Locais de estudo
-
-
-
Prague, Tcheca, 12808
- Recrutamento
- General University Hospital
-
Contato:
- Jan Vávra, Masters
- Número de telefone: +420601200272
- E-mail: vavrajan1@gmail.com
-
Contato:
- Vladimír Tuka, doc
- E-mail: Vladimir.Tuka@vfn.cz
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Confirmed diagnosis of Fabry disease
- Age 18 years or older
- Followed at a participating clinical center
- Able to understand the study procedures and provide informed consent
- Clinically stable and medically suitable for exercise testing and participation in the exercise programme
Exclusion Criteria:
- Acute deterioration in health status at the time of enrollment
- Medical contraindication to exercise testing or exercise training
- Severe comorbidity preventing safe participation in the study procedures
- Inability to comply with study procedures or complete follow-up assessments
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Exercise Intervention Group
Participants will complete a 12-week physiotherapy-led exercise programme consisting of one supervised exercise session per week and two home-based exercise sessions per week, together with a progressive increase in daily step count. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. Participants will be assessed at baseline, immediately after the 12-week intervention, and 12 months after baseline. |
A 12-week physiotherapy-led exercise programme consisting of one supervised session and two home-based exercise sessions per week. Supervised sessions include a brief aerobic warm-up followed by strengthening exercises using body weight and resistance bands. The programme also includes a progressive increase in daily ambulatory physical activity, monitored primarily by daily step count. Adherence is monitored using exercise diaries and regular follow-up during supervised sessions. |
|
Sem intervenção: Control Group
Participants will receive no study-specific exercise intervention. They will be assessed at baseline and 12 months after baseline. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change from baseline in peak oxygen uptake (VO2peak) after 12 weeks
Prazo: Baseline and 12 weeks after baseline
|
Change from baseline in peak oxygen uptake (VO2peak), expressed in mL/kg/min, assessed during cardiopulmonary exercise testing (CPET) in the exercise intervention group following the 12-week exercise programme. |
Baseline and 12 weeks after baseline
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change from baseline in peak oxygen uptake (VO2peak) at 12 months
Prazo: Baseline and 12 months after baseline
|
Change from baseline in peak oxygen uptake (VO2peak), expressed in mL/kg/min, assessed during cardiopulmonary exercise testing (CPET). VO2peak will be assessed at baseline and 12 months after baseline in both the exercise intervention and control groups. The change over 12 months will be compared between groups. |
Baseline and 12 months after baseline
|
|
Change in handgrip strength
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in handgrip strength, expressed in kilograms, assessed using handgrip dynamometry. Participants will be assessed in a seated position with the arm close to the body and the elbow flexed at approximately 90 degrees. Three maximal trials will be performed for each hand. The highest value from each hand will be retained, and the mean of the highest right- and left-hand values will be used as the handgrip strength outcome. In the intervention group, handgrip strength will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, handgrip strength will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in 6-minute walk distance
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in distance walked during the 6-minute walk test, expressed in meters. In the intervention group, the 6-minute walk distance will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the 6-minute walk distance will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in 30-second chair stand test performance
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in the number of completed stands during the 30-second chair stand test. In the intervention group, performance will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, performance will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in forced expiratory volume in 1 second (FEV1)
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in forced expiratory volume in 1 second (FEV1), expressed in liters, assessed by pulmonary function testing. In the intervention group, FEV1 will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, FEV1 will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in vital capacity (VC)
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in vital capacity (VC), expressed in liters, assessed by pulmonary function testing. In the intervention group, VC will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, VC will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in diffusing capacity of the lungs for carbon monoxide (DLCO)
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in diffusing capacity of the lungs for carbon monoxide (DLCO), expressed in mmol/min/kPa, assessed by pulmonary function testing. In the intervention group, DLCO will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, DLCO will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in Hospital Anxiety and Depression Scale - Anxiety subscale score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in anxiety symptoms assessed using the Anxiety subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, resulting in a total score ranging from 0 to 21. Higher scores indicate greater severity of anxiety symptoms. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in Hospital Anxiety and Depression Scale - Depression subscale score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in depressive symptoms assessed using the Depression subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, resulting in a total score ranging from 0 to 21. Higher scores indicate greater severity of depressive symptoms. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Physical Functioning domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in physical functioning assessed using the Physical Functioning domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 10 items and is scored from 0 to 100, with higher scores indicating better physical functioning. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Role Physical domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in limitations in usual role activities due to physical health problems assessed using the Role Physical domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 4 items and is scored from 0 to 100, with higher scores indicating fewer limitations due to physical health problems. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Bodily Pain domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in bodily pain assessed using the Bodily Pain domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 2 items and is scored from 0 to 100, with higher scores indicating less pain and less interference of pain with usual activities. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 General Health domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in general health perceptions assessed using the General Health domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 5 items and is scored from 0 to 100, with higher scores indicating better perceived general health. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Vitality domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in vitality assessed using the Vitality domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 4 items and is scored from 0 to 100, with higher scores indicating greater vitality and lower levels of fatigue. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Social Functioning domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in social functioning assessed using the Social Functioning domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 2 items and is scored from 0 to 100, with higher scores indicating better social functioning and less interference of health problems with social activities. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Role Emotional domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in limitations in usual role activities due to emotional problems assessed using the Role Emotional domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 3 items and is scored from 0 to 100, with higher scores indicating fewer role limitations due to emotional problems. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in SF-36 Mental Health domain score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in mental health assessed using the Mental Health domain of the 36-Item Short Form Health Survey (SF-36). The domain consists of 5 items and is scored from 0 to 100, with higher scores indicating better mental health and psychological well-being. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in EQ-5D-5L health state index value
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in health-related quality of life assessed using the EQ-5D-5L descriptive system. The instrument assesses five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each rated across five levels of severity. Responses will be converted to an EQ-5D-5L health state index value using an appropriate validated value set. Higher index values indicate better health-related quality of life. In the intervention group, the index value will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the index value will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in EQ-5D-5L Visual Analogue Scale score
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in self-rated health assessed using the EQ-5D-5L Visual Analogue Scale (EQ VAS). The scale ranges from 0 to 100, where 0 represents the worst health the participant can imagine and 100 represents the best health the participant can imagine. Higher scores indicate better self-rated health. In the intervention group, the score will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, the score will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in skeletal muscle mass
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in skeletal muscle mass, expressed in kilograms, assessed by bioelectrical impedance analysis using the InBody970 device. In the intervention group, skeletal muscle mass will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, skeletal muscle mass will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in body fat mass
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in body fat mass, expressed in kilograms, assessed by bioelectrical impedance analysis using the InBody970 device. In the intervention group, body fat mass will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, body fat mass will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
|
Change in whole-body phase angle
Prazo: Baseline, 12 weeks after baseline, and 12 months after baseline
|
Change in whole-body phase angle, expressed in degrees, assessed at 50 kHz by bioelectrical impedance analysis using the InBody970 device. In the intervention group, whole-body phase angle will be assessed at baseline, immediately after the 12-week exercise intervention, and 12 months after baseline. In the control group, whole-body phase angle will be assessed at baseline and 12 months after baseline. |
Baseline, 12 weeks after baseline, and 12 months after baseline
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Distúrbios Cerebrovasculares
- Doenças Cerebrais
- Doenças do Sistema Nervoso Central
- Doenças do Sistema Nervoso
- Doenças Vasculares
- Doenças cardiovasculares
- Metabolismo, Erros Inatos
- Doenças Genéticas, Congênitas
- Doenças Metabólicas
- Distúrbios do metabolismo lipídico
- Doenças Genéticas, Ligadas ao X
- Doenças de Armazenamento Lisossomal
- Doenças Cerebrais Metabólicas Inatas
- Doenças Cerebrais Metabólicas
- Metabolismo Lipídico, Erros Inatos
- Doenças do Armazenamento Lisossomal, Sistema Nervoso
- Doenças Cerebrais de Pequenos Vasos
- Esfingolipidoses
- Lipidoses
- Doenças e Anormalidades Congênitas, Hereditárias e Neonatais
- Comportamento
- Doenças Nutricionais e Metabólicas
- Doença de Fabry
- Atividade motora
Outros números de identificação do estudo
- A-FAD-FIT
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
There is currently no plan to share individual participant data. Any future data sharing would require separate consideration in accordance with applicable ethics, participant consent, and data protection requirements.
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
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 .