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NCT Number: NCT07576751

Physiotherapy Practice in Flemish Nursing Homes

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.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Nursing home, Deurne, Antwerpen, Belgium

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • None

Treatment and study plan

Mapping therapy sessions

Other

Mapping therapy sessions provided by physical therapists in Flemish nursing homes

Primary outcomes

  1. Guideline Adherence to IAGG-GARN Recommendations

    Time frame: 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)

Secondary outcomes

  1. Exercise Description

    Time frame: 2 weeks

    Narrative description of each exercise performed during a physiotherapy sessions.

  2. Use of Equipment, Aids or Materials

    Time frame: 2 weeks

    Type of equipment, aids or materials used during each exercise.

  3. Exercise format

    Time frame: 2 weeks

    Whether the exercise is performed individually or in a group setting.

  4. Group Size

    Time frame: 2 weeks

    Number of participants involved in group-based exercises.

  5. Level of supervision

    Time frame: 2 weeks

    Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)

  6. Exercise Start and End Time

    Time frame: 2 weeks

    Start and end time of each exercise performed during physiotherapy sessions

  7. Rest Periods During Exercises

    Time frame: 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.

  8. Exercise Category

    Time frame: 2 weeks

    Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)

  9. Exercise Volume - Repetitions

    Time frame: 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.

  10. Exercise Intensity

    Time frame: 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).

  11. Walking or Treadmill parameters

    Time frame: 2 weeks

    Parameters during walking or treadmill exercises (incline and speed).

  12. Cycling Parameters

    Time frame: 2 weeks

    Parameters recorded during cycling exercises (rounds per minute, resistance and distance)

  13. Speed of movement

    Time frame: 2 weeks

    Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).

  14. External Load (Resistance)

    Time frame: 2 weeks

    External load applied during exercises (kg).

  15. Contextual Factors

    Time frame: 2 weeks

    Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.

Other outcomes

  1. Background information physiotherapists

    Time frame: 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.

  2. Background information residents

    Time frame: 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
  3. Focus groups with physiotherapists

    Time frame: 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Joke Spildooren, Prof.dr

CONTACT

[email protected]

+3211269178

Maxine Claes, Msc

CONTACT

[email protected]

+3211268443

Sponsors and collaborators

Lead sponsor

Hasselt University

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
May 8, 2026
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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