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Guideline ImplementationNCT07576751

Physiotherapy Practice in Flemish Nursing Homes

An observational study of Guideline Implementation and Physiotherapy, run by Hasselt University at 3 sites in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
What is being tested?
Mapping therapy sessions
How many people
40 participants
Where
3 sitesBelgium
Study dates
23 Mar 2026to 1 Dec 2028
How long will I take part?
2 Weeks
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

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

Who may be able to join

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

Who cannot join

  • None

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Maxine Claes, Msc contact

+3211268443

maxine.claes@uhasselt.be

Joke Spildooren, Prof.dr contact

+3211269178

joke.spildooren@uhasselt.be

Belgium3 sites, 3 recruiting
  • Nursing home

    Deurne, Antwerpen

    Not yet recruiting
  • Nursing home

    Tongeren, Limburg

    Recruiting
  • Nursing home

    Zoersel, Antwerpen

    Recruiting

Other trials in Belgium

About this study

Official title: 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.

Read more

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.

Being tested
Mapping therapy sessions
Keywords
Physical therapy, Older adults, Geriatrics, Long-term care, Guideline implementation, Focus groups, Clinical practice

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mapping therapy sessionsOther

    Mapping therapy sessions provided by physical therapists in Flemish nursing homes

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Guideline Adherence to IAGG-GARN Recommendations

    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)

    Measured: 2 weeks

Secondary outcomes (15)
  1. Exercise Description

    Narrative description of each exercise performed during a physiotherapy sessions.

    Measured: 2 weeks

  2. Use of Equipment, Aids or Materials

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

    Measured: 2 weeks

  3. Exercise format

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

    Measured: 2 weeks

  4. Group Size

    Number of participants involved in group-based exercises.

    Measured: 2 weeks

  5. Level of supervision

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

    Measured: 2 weeks

  6. Exercise Start and End Time

    Start and end time of each exercise performed during physiotherapy sessions

    Measured: 2 weeks

  7. Rest Periods During Exercises

    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.

    Measured: 2 weeks

  8. Exercise Category

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

    Measured: 2 weeks

  9. Exercise Volume - Repetitions

    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.

    Measured: 2 weeks

  10. Exercise Intensity

    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).

    Measured: 2 weeks

  11. Walking or Treadmill parameters

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

    Measured: 2 weeks

  12. Cycling Parameters

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

    Measured: 2 weeks

  13. Speed of movement

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

    Measured: 2 weeks

  14. External Load (Resistance)

    External load applied during exercises (kg).

    Measured: 2 weeks

  15. Contextual Factors

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

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 May 2026
  2. Study start23 Mar 2026
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (estimated)
Target duration
2 Weeks
IDs, dates and publications
ClinicalTrials.gov ID
NCT07576751
Sponsor's protocol ID
B1152025000037
Other IDs
BOF25OWB11
Status last verified
May 2026
First submitted
2 Apr 2026
Last updated
8 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Guideline Implementation and Physiotherapy, run by Hasselt University at 3 sites in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 8 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Maxine Claes, Msc (+3211268443, maxine.claes@uhasselt.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Guideline Adherence to IAGG-GARN Recommendations (time frame: 2 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 May 2026.

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