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Physical and Cognitive Outcomes After Post-Transplant Physiotherapy in Liver Transplant Recipients

9 de julho de 2026 atualizado por: İlker DEMİR, Hasan Kalyoncu University

Evaluation of Physical and Cognitive Outcomes in Liver Transplant Recipients Who Participated in a Post-Transplant Physiotherapy Program

Liver transplantation is the most effective treatment for end-stage liver disease. However, many recipients continue to experience problems such as reduced physical function, impaired balance, fatigue, and cognitive difficulties even after successful transplantation. Although physiotherapy is commonly provided during the early postoperative period, its long-term benefits are not well understood.

This observational cross-sectional study evaluated the long-term physical and cognitive outcomes of adult liver transplant recipients approximately one year after transplantation. A total of 106 participants were included and divided into two groups according to whether they had participated in a routine post-transplant physiotherapy and rehabilitation program. Physical performance, balance, functional exercise capacity, cognitive function, and fatigue were assessed using standardized clinical outcome measures.

The study aimed to determine whether participation in a routine physiotherapy program was associated with better long-term functional outcomes after liver transplantation. The findings may help improve long-term rehabilitation strategies and support the integration of physiotherapy into routine multidisciplinary follow-up care for liver transplant recipients.

Visão geral do estudo

Descrição detalhada

Detailed Description

Liver transplantation is the standard treatment for end-stage liver disease and has substantially improved long-term survival. As survival has increased, greater attention has been directed toward long-term functional recovery, including the restoration of physical performance, cognitive function, and independence in daily living. Despite successful transplantation, many recipients continue to experience persistent impairments such as reduced mobility, balance deficits, fatigue, and cognitive dysfunction, which may negatively affect quality of life and long-term health outcomes.

Physiotherapy and rehabilitation are widely recommended during the postoperative period to promote recovery and prevent complications. Although previous studies have demonstrated the short-term benefits of rehabilitation after liver transplantation, evidence regarding its long-term effects remains limited. In particular, few studies have evaluated whether improvements achieved during the early postoperative period are maintained approximately one year after transplantation.

This observational cross-sectional study was conducted to evaluate the long-term physical and cognitive outcomes of liver transplant recipients who had participated in a routine post-transplant physiotherapy program compared with recipients who had not received postoperative physiotherapy. The study assessed functional mobility, balance, functional exercise capacity, cognitive performance, and fatigue using standardized clinical assessment tools.

The findings of this study are expected to provide further evidence regarding the long-term contribution of routine physiotherapy to functional recovery after liver transplantation and to support the development of multidisciplinary rehabilitation strategies for transplant recipients.

Tipo de estudo

Observacional

Inscrição (Real)

106

Contactos e Locais

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Locais de estudo

      • Malatya, Turquia (Türkiye), 44280
        • Liver Transplant Institute Hospital, Turgut Özal Medical Center, İnönü University

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
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

Adult liver transplant recipients who underwent liver transplantation at Turgut Özal Medical Center, İnönü University, and were evaluated approximately one year after transplantation. Participants were classified according to whether they had participated in a routine post-transplant physiotherapy and rehabilitation program.

Descrição

Inclusion Criteria:

  • Adult liver transplant recipients aged 18 years or older.
  • At least 1 year since liver transplantation.
  • Spontaneous breathing.
  • Hemodynamically stable.
  • Able to read and write.
  • Willing and able to provide written informed consent.

Exclusion Criteria:

  • History of a neurological disorder.
  • Presence of a neuropsychiatric disorder.
  • Orthopedic or rheumatologic conditions that could interfere with the assessments.
  • Advanced cardiopulmonary disease.
  • Visual or hearing impairment that prevented completion of the assessments. Refusal to participate in the study.

Plano de estudo

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Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
Routine Physiotherapy Group
Adult liver transplant recipients who completed the routine post-transplant physiotherapy and rehabilitation program. Participants were assessed approximately one year after liver transplantation.
Participation in the routine postoperative physiotherapy and rehabilitation program provided after liver transplantation as part of standard clinical care. The program included breathing exercises, progressive mobilization, muscle strengthening, balance training, gait training, and functional exercises. Participants were not assigned to this intervention by the study protocol; the intervention had been completed before enrollment in this observational study.
Control Group
Adult liver transplant recipients who did not participate in any postoperative physiotherapy or rehabilitation program and were evaluated approximately one year after transplantation.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Functional Mobility
Prazo: Approximately 1 year after liver transplantation
Functional mobility assessed using the Timed Up and Go (TUG) Test. The outcome is recorded as the time required to complete the test, measured in seconds (minimum possible value: 0 seconds; no predefined maximum value). Lower completion times indicate better functional mobility.
Approximately 1 year after liver transplantation
Static Balance
Prazo: Approximately 1 year after liver transplantation
Static balance assessed using the Single-Leg Stance Test. Participants were instructed to stand on their dominant leg for as long as possible while maintaining balance. The duration of single-leg stance was recorded in seconds (minimum possible value: 0 seconds; no predefined maximum value), and the best performance was used for analysis. Longer standing times indicate better static balance.
Approximately 1 year after liver transplantation
Cognitive Function
Prazo: Approximately 1 year after liver transplantation
Cognitive function assessed using the Montreal Cognitive Assessment (MoCA). Scores range from 0 to 30, with higher scores indicating better cognitive performance.
Approximately 1 year after liver transplantation

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Functional Exercise Capacity
Prazo: Approximately 1 year after liver transplantation
Functional exercise capacity assessed using the Six-Minute Walk Test (6MWT). Walking distance was measured in meters (minimum possible value: 0 meters; no predefined maximum value). Greater walking distances indicate better functional exercise capacity.
Approximately 1 year after liver transplantation
Fatigue Severity
Prazo: Approximately 1 year after liver transplantation
Fatigue severity assessed using the Fatigue Severity Scale (FSS). Total scores range from 9 to 63, with higher scores indicating greater fatigue severity.
Approximately 1 year after liver transplantation

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)

27 de outubro de 2024

Conclusão Primária (Real)

15 de junho de 2026

Conclusão do estudo (Real)

15 de junho de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

3 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

3 de julho de 2026

Primeira postagem (Real)

9 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

10 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

9 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

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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