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Physiotherapy Practice in Flemish Nursing Homes

4 maj 2026 uppdaterad av: 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.

Studieöversikt

Status

Rekrytering

Intervention / Behandling

Studietyp

Observationell

Inskrivning (Beräknad)

40

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Studieorter

    • Antwerpen
      • Deurne, Antwerpen, Belgien
        • Har inte rekryterat ännu
        • Nursing home
      • Zoersel, Antwerpen, Belgien
        • Rekrytering
        • Nursing home
    • Limburg
      • Tongeren, Limburg, Belgien
        • Rekrytering
        • Nursing home

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Testmetod

Icke-sannolikhetsprov

Studera befolkning

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

Beskrivning

Inclusion Criteria:

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

Exclusion Criteria:

  • None

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Guideline Adherence to IAGG-GARN Recommendations
Tidsram: 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

Sekundära resultatmått

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

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Background information physiotherapists
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Joke Spildooren, Prof.dr, UHasselt

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

23 mars 2026

Primärt slutförande (Beräknad)

1 januari 2028

Avslutad studie (Beräknad)

1 december 2028

Studieregistreringsdatum

Först inskickad

2 april 2026

Först inskickad som uppfyllde QC-kriterierna

4 maj 2026

Första postat (Faktisk)

8 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

8 maj 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

4 maj 2026

Senast verifierad

1 maj 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • B1152025000037
  • BOF25OWB11 (Annat bidrag/finansieringsnummer: Bijzonder Onderzoekfonds (BOF))

Läkemedels- och apparatinformation, studiedokument

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