- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07576751
Physiotherapy Practice in Flemish Nursing Homes
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.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Maxine Claes, Msc
- Número de teléfono: +3211268443
- Correo electrónico: maxine.claes@uhasselt.be
Copia de seguridad de contactos de estudio
- Nombre: Joke Spildooren, Prof.dr
- Número de teléfono: +3211269178
- Correo electrónico: joke.spildooren@uhasselt.be
Ubicaciones de estudio
-
-
Antwerpen
-
Deurne, Antwerpen, Bélgica
- Aún no reclutando
- Nursing home
-
Zoersel, Antwerpen, Bélgica
- Reclutamiento
- Nursing home
-
-
Limburg
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Tongeren, Limburg, Bélgica
- Reclutamiento
- Nursing home
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- None beyond being a licensed physiotherapist working in a Flemish nursing home and willing to participate.
Exclusion Criteria:
- None
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Guideline Adherence to IAGG-GARN Recommendations
Periodo de tiempo: 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 resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Exercise Description
Periodo de tiempo: 2 weeks
|
Narrative description of each exercise performed during a physiotherapy sessions.
|
2 weeks
|
|
Use of Equipment, Aids or Materials
Periodo de tiempo: 2 weeks
|
Type of equipment, aids or materials used during each exercise.
|
2 weeks
|
|
Exercise format
Periodo de tiempo: 2 weeks
|
Whether the exercise is performed individually or in a group setting.
|
2 weeks
|
|
Group Size
Periodo de tiempo: 2 weeks
|
Number of participants involved in group-based exercises.
|
2 weeks
|
|
Level of supervision
Periodo de tiempo: 2 weeks
|
Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)
|
2 weeks
|
|
Exercise Start and End Time
Periodo de tiempo: 2 weeks
|
Start and end time of each exercise performed during physiotherapy sessions
|
2 weeks
|
|
Rest Periods During Exercises
Periodo de tiempo: 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
Periodo de tiempo: 2 weeks
|
Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)
|
2 weeks
|
|
Exercise Volume - Repetitions
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 2 weeks
|
Parameters during walking or treadmill exercises (incline and speed).
|
2 weeks
|
|
Cycling Parameters
Periodo de tiempo: 2 weeks
|
Parameters recorded during cycling exercises (rounds per minute, resistance and distance)
|
2 weeks
|
|
Speed of movement
Periodo de tiempo: 2 weeks
|
Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).
|
2 weeks
|
|
External Load (Resistance)
Periodo de tiempo: 2 weeks
|
External load applied during exercises (kg).
|
2 weeks
|
|
Contextual Factors
Periodo de tiempo: 2 weeks
|
Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.
|
2 weeks
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Background information physiotherapists
Periodo de tiempo: 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
Periodo de tiempo: 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:
|
baseline
|
|
Focus groups with physiotherapists
Periodo de tiempo: 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
Patrocinador
Investigadores
- Investigador principal: Joke Spildooren, Prof.dr, UHasselt
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- B1152025000037
- BOF25OWB11 (Otro número de subvención/financiamiento: Bijzonder Onderzoekfonds (BOF))
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
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