- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Maxine Claes, Msc
- Phone Number: +3211268443
- Email: maxine.claes@uhasselt.be
Study Contact Backup
- Name: Joke Spildooren, Prof.dr
- Phone Number: +3211269178
- Email: joke.spildooren@uhasselt.be
Study Locations
-
-
Antwerpen
-
Deurne, Antwerpen, Belgium
- Not yet recruiting
- Nursing home
-
Zoersel, Antwerpen, Belgium
- Recruiting
- Nursing home
-
-
Limburg
-
Tongeren, Limburg, Belgium
- Recruiting
- Nursing home
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- None beyond being a licensed physiotherapist working in a Flemish nursing home and willing to participate.
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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)
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exercise Description
Time Frame: 2 weeks
|
Narrative description of each exercise performed during a physiotherapy sessions.
|
2 weeks
|
|
Use of Equipment, Aids or Materials
Time Frame: 2 weeks
|
Type of equipment, aids or materials used during each exercise.
|
2 weeks
|
|
Exercise format
Time Frame: 2 weeks
|
Whether the exercise is performed individually or in a group setting.
|
2 weeks
|
|
Group Size
Time Frame: 2 weeks
|
Number of participants involved in group-based exercises.
|
2 weeks
|
|
Level of supervision
Time Frame: 2 weeks
|
Level of supervision provided by the physiotherapist during exercises (none, intermittent, continuous)
|
2 weeks
|
|
Exercise Start and End Time
Time Frame: 2 weeks
|
Start and end time of each exercise performed during physiotherapy sessions
|
2 weeks
|
|
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.
|
2 weeks
|
|
Exercise Category
Time Frame: 2 weeks
|
Category of each exercise performed during physiotherapy sessions (strength, endurance, mobility/flexibility, balance/coordination, or other)
|
2 weeks
|
|
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.
|
2 weeks
|
|
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).
|
2 weeks
|
|
Walking or Treadmill parameters
Time Frame: 2 weeks
|
Parameters during walking or treadmill exercises (incline and speed).
|
2 weeks
|
|
Cycling Parameters
Time Frame: 2 weeks
|
Parameters recorded during cycling exercises (rounds per minute, resistance and distance)
|
2 weeks
|
|
Speed of movement
Time Frame: 2 weeks
|
Speed of movement during exercises, classified according to the observed execution pace (slow, controlled or fast).
|
2 weeks
|
|
External Load (Resistance)
Time Frame: 2 weeks
|
External load applied during exercises (kg).
|
2 weeks
|
|
Contextual Factors
Time Frame: 2 weeks
|
Contextual elements influencing physiotherapy sessions, such as disturbances (e.g., noise, interruptions) and other relevant observations.
|
2 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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. |
baseline
|
|
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:
|
baseline
|
|
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. |
2 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Joke Spildooren, Prof.dr, UHasselt
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- B1152025000037
- BOF25OWB11 (Other Grant/Funding Number: Bijzonder Onderzoekfonds (BOF))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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