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Physiotherapy Practice in Flemish Nursing Homes

4 de maio de 2026 atualizado por: Joke Spildooren, Hasselt University

Physiotherapy in Flemish Nursing Homes: Insights Into Practice, Barriers, and Facilitators

The goal of this observational study is to evaluate the extent to which physiotherapy sessions in Flemish nursing homes adhere to the IAGG-GARN guidelines and to explore factors influencing clinical practice among physiotherapists.

The study targets multiple nursing homes across Flanders, with 3 to 5 centers in each of the provinces of Limburg, Antwerp, and Flemish Brabant. This selection ensures variation in geographic location and organizational context. The participants in this study are physiotherapists working in the participating nursing homes.

The main questions it aims to answer are:

  • To what extent do the physiotherapy sessions align with the IAGG-GARN guidelines?
  • Are there differences in physiotherapy session content and volume according to physiotherapist characteristics and resident characteristics?
  • What barriers and facilitators do physiotherapists experience when implementing guideline-based practice in Flemish nursing homes?

Researchers will observe physiotherapy sessions delivered as part of routine care and document session content and duration using structured observation diaries. Participating physiotherapists will also take part in focus groups discussing experiences with guideline implementation, barriers, facilitators, and clinical decision-making.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Tipo de estudo

Observacional

Inscrição (Estimado)

40

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

Estude backup de contato

Locais de estudo

    • Antwerpen
      • Deurne, Antwerpen, Bélgica
        • Ainda não está recrutando
        • Nursing home
      • Zoersel, Antwerpen, Bélgica
        • Recrutamento
        • Nursing home
    • Limburg
      • Tongeren, Limburg, Bélgica
        • Recrutamento
        • Nursing home

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

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Método de amostragem

Amostra Não Probabilística

População do estudo

The study population consists of licensed physiotherapists working in Flemish nursing homes who provide physiotherapy to older residents

Descrição

Inclusion Criteria:

  • None beyond being a licensed physiotherapist working in a Flemish nursing home and willing to participate.

Exclusion Criteria:

  • None

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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Guideline Adherence to IAGG-GARN Recommendations
Prazo: 2 weeks
Overall adherence of physiotherapy sessions in Flemish nursing homes to IAGG-GARN recommendations. Adherence is assessed through structured direct observation of the routine physiotherapy sessions. The secondary outcomes are operationalize adherence to the guideline (frequency, exercise intensity, exercise duration, exercise type and personalization)
2 weeks

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Exercise Description
Prazo: 2 weeks
Narrative description of each exercise performed during a physiotherapy sessions.
2 weeks
Use of Equipment, Aids or Materials
Prazo: 2 weeks
Type of equipment, aids or materials used during each exercise.
2 weeks
Exercise format
Prazo: 2 weeks
Whether the exercise is performed individually or in a group setting.
2 weeks
Group Size
Prazo: 2 weeks
Number of participants involved in group-based exercises.
2 weeks
Level of supervision
Prazo: 2 weeks
Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)
2 weeks
Exercise Start and End Time
Prazo: 2 weeks
Start and end time of each exercise performed during physiotherapy sessions
2 weeks
Rest Periods During Exercises
Prazo: 2 weeks
Rest periods during physiotherapy exercises, recorded separately as (1) rest periods instructed or allowed by the physiotherapist and (2) rest periods actually taken by the resident during exercise.
2 weeks
Exercise Category
Prazo: 2 weeks
Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)
2 weeks
Exercise Volume - Repetitions
Prazo: 2 weeks
Number of repetitions per exercise, recorded separately as (1) repetitions prescribed by the physiotherapist and (2) repetitions actually performed by the resident during the exercise.
2 weeks
Exercise Intensity
Prazo: 2 weeks
Intensity of each exercise performed during physiotherapy sessions, including whether intensity was explicitly determined during the exercise, the method used to determine intensity, the recorded intensity value, and the observer's interpretation (high, medium or low intensity).
2 weeks
Walking or Treadmill parameters
Prazo: 2 weeks
Parameters during walking or treadmill exercises (incline and speed).
2 weeks
Cycling Parameters
Prazo: 2 weeks
Parameters recorded during cycling exercises (rounds per minute, resistance and distance)
2 weeks
Speed of movement
Prazo: 2 weeks
Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).
2 weeks
External Load (Resistance)
Prazo: 2 weeks
External load applied during exercises (kg).
2 weeks
Contextual Factors
Prazo: 2 weeks
Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.
2 weeks

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Background information physiotherapists
Prazo: baseline

Age, gender, year of graduation, specialization, number of years of experience as a physiotherapist, educational level (e.g., bachelor, master…), employment regime (full-time, part-time, other appointment), number of years working within the nursing home and continuing education participation

This information is pseudonymously linked to the observation data with the aim of identifying interpersonal differences in therapy approach.

baseline
Background information residents
Prazo: baseline

In addition, the physiotherapeutic interventions will be linked to residents' background information to determine the extent to which the physiotherapists adapt their therapy to the specific needs of the patient. The following information will be used:

  • Age category: 65-70, 71-75, 76-80, 81-85, 86-90, 91-95, 96-100 and 100+
  • Gender: male / female / other
  • Stable medical status: yes/no
  • Cognitive status (MMSE score): 25-30 (normal), 21-24 (mild cognitive impairment), 10-20 (moderate cognitive impairment), 0-9 (severe cognitive impairment)
  • Ability to walk (maximum achievable level for resident): independent, independent with walking aid, with assistance from caregiver, wheelchair-bound, bedridden
  • Ability to transfer (maximum achievable level for resident): independent, with aid, with assistance from caregiver, with hoist
  • Following physiotherapy: yes/no
  • With which (main) physiotherapist: physiotherapist ID
baseline
Focus groups with physiotherapists
Prazo: 2 days

Step 1: Center-specific After completion of the observations, a center-specific feedback session will be held at each nursing home. These sessions (60-90 minutes, 2-8 therapists) present and discuss the results with physiotherapists, focusing on their work context, its influence on care delivery, and the reasoning behind their choices.

Step 2: Validation Following the feedback sessions, a validation focus group will be organized at a neutral location (UHasselt), including 1-2 representatives per center and additional physiotherapists (10 participants, 60-90 minutes). Results from the observations and all feedback sessions will be presented anonymously. The discussion will focus on validating and deepening findings, identifying key themes and patterns, and determining priorities for further development

Digital recordings of the focus groups will be made during the session. At the end of the focus groups, the recordings will be transcribed and anonymized for analysis.

2 days

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Joke Spildooren, Prof.dr, UHasselt

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)

23 de março de 2026

Conclusão Primária (Estimado)

1 de janeiro de 2028

Conclusão do estudo (Estimado)

1 de dezembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

2 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

4 de maio de 2026

Primeira postagem (Real)

8 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

4 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • B1152025000037
  • BOF25OWB11 (Número de outro subsídio/financiamento: Bijzonder Onderzoekfonds (BOF))

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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