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Physiotherapy Practice in Flemish Nursing Homes

4 mei 2026 bijgewerkt door: 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.

Studie Overzicht

Studietype

Observationeel

Inschrijving (Geschat)

40

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

    • Antwerpen
      • Deurne, Antwerpen, België
        • Nog niet aan het werven
        • Nursing home
      • Zoersel, Antwerpen, België
        • Werving
        • Nursing home
    • Limburg
      • Tongeren, Limburg, België
        • Werving
        • Nursing home

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Bemonsteringsmethode

Niet-waarschijnlijkheidssteekproef

Studie Bevolking

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

Beschrijving

Inclusion Criteria:

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

Exclusion Criteria:

  • None

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Guideline Adherence to IAGG-GARN Recommendations
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Exercise Description
Tijdsspanne: 2 weeks
Narrative description of each exercise performed during a physiotherapy sessions.
2 weeks
Use of Equipment, Aids or Materials
Tijdsspanne: 2 weeks
Type of equipment, aids or materials used during each exercise.
2 weeks
Exercise format
Tijdsspanne: 2 weeks
Whether the exercise is performed individually or in a group setting.
2 weeks
Group Size
Tijdsspanne: 2 weeks
Number of participants involved in group-based exercises.
2 weeks
Level of supervision
Tijdsspanne: 2 weeks
Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)
2 weeks
Exercise Start and End Time
Tijdsspanne: 2 weeks
Start and end time of each exercise performed during physiotherapy sessions
2 weeks
Rest Periods During Exercises
Tijdsspanne: 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
Tijdsspanne: 2 weeks
Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)
2 weeks
Exercise Volume - Repetitions
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 2 weeks
Parameters during walking or treadmill exercises (incline and speed).
2 weeks
Cycling Parameters
Tijdsspanne: 2 weeks
Parameters recorded during cycling exercises (rounds per minute, resistance and distance)
2 weeks
Speed of movement
Tijdsspanne: 2 weeks
Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).
2 weeks
External Load (Resistance)
Tijdsspanne: 2 weeks
External load applied during exercises (kg).
2 weeks
Contextual Factors
Tijdsspanne: 2 weeks
Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.
2 weeks

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Background information physiotherapists
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Joke Spildooren, Prof.dr, UHasselt

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

23 maart 2026

Primaire voltooiing (Geschat)

1 januari 2028

Studie voltooiing (Geschat)

1 december 2028

Studieregistratiedata

Eerst ingediend

2 april 2026

Eerst ingediend dat voldeed aan de QC-criteria

4 mei 2026

Eerst geplaatst (Werkelijk)

8 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

8 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

4 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • B1152025000037
  • BOF25OWB11 (Ander subsidie-/financieringsnummer: Bijzonder Onderzoekfonds (BOF))

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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