- ICH GCP
- Registre américain des essais cliniques
- Essai clinique 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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Maxine Claes, Msc
- Numéro de téléphone: +3211268443
- E-mail: maxine.claes@uhasselt.be
Sauvegarde des contacts de l'étude
- Nom: Joke Spildooren, Prof.dr
- Numéro de téléphone: +3211269178
- E-mail: joke.spildooren@uhasselt.be
Lieux d'étude
-
-
Antwerpen
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Deurne, Antwerpen, Belgique
- Pas encore de recrutement
- Nursing home
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Zoersel, Antwerpen, Belgique
- Recrutement
- Nursing home
-
-
Limburg
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Tongeren, Limburg, Belgique
- Recrutement
- Nursing home
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- None beyond being a licensed physiotherapist working in a Flemish nursing home and willing to participate.
Exclusion Criteria:
- None
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Guideline Adherence to IAGG-GARN Recommendations
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Exercise Description
Délai: 2 weeks
|
Narrative description of each exercise performed during a physiotherapy sessions.
|
2 weeks
|
|
Use of Equipment, Aids or Materials
Délai: 2 weeks
|
Type of equipment, aids or materials used during each exercise.
|
2 weeks
|
|
Exercise format
Délai: 2 weeks
|
Whether the exercise is performed individually or in a group setting.
|
2 weeks
|
|
Group Size
Délai: 2 weeks
|
Number of participants involved in group-based exercises.
|
2 weeks
|
|
Level of supervision
Délai: 2 weeks
|
Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)
|
2 weeks
|
|
Exercise Start and End Time
Délai: 2 weeks
|
Start and end time of each exercise performed during physiotherapy sessions
|
2 weeks
|
|
Rest Periods During Exercises
Délai: 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
Délai: 2 weeks
|
Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)
|
2 weeks
|
|
Exercise Volume - Repetitions
Délai: 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
Délai: 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
Délai: 2 weeks
|
Parameters during walking or treadmill exercises (incline and speed).
|
2 weeks
|
|
Cycling Parameters
Délai: 2 weeks
|
Parameters recorded during cycling exercises (rounds per minute, resistance and distance)
|
2 weeks
|
|
Speed of movement
Délai: 2 weeks
|
Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).
|
2 weeks
|
|
External Load (Resistance)
Délai: 2 weeks
|
External load applied during exercises (kg).
|
2 weeks
|
|
Contextual Factors
Délai: 2 weeks
|
Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.
|
2 weeks
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Background information physiotherapists
Délai: 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
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Joke Spildooren, Prof.dr, UHasselt
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- B1152025000037
- BOF25OWB11 (Autre subvention/numéro de financement: Bijzonder Onderzoekfonds (BOF))
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
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