Actively Recruiting
Physiotherapy in Flemish Nursing Homes: Insights Into Practice, Barriers, and Facilitators
Led by Hasselt University · Updated on 2026-05-08
40
Participants Needed
3
Research Sites
47 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating how well physiotherapy sessions in Flemish nursing homes follow the IAGG-GARN guidelines and what factors influence physiotherapists' clinical practices. The study focuses on multiple nursing homes across the provinces of Limburg, Antwerp, and Flemish Brabant to capture a variety of geographic and organizational settings. It aims to understand the content and volume differences in physiotherapy sessions and to identify challenges and supports physiotherapists face when applying these guidelines. The study involves observing routine physiotherapy sessions delivered by licensed physiotherapists in these nursing homes. Researchers will document session details such as content, duration, exercise type, use of equipment, supervision levels, intensity, and other factors over a two-week period using structured diaries. Participating physiotherapists will also join focus groups to discuss their experiences, barriers, facilitators, and decision-making related to guideline-based care. Participants will be monitored through direct observation and focus group discussions. The main outcome is the adherence to IAGG-GARN guidelines within two weeks. Secondary measures include detailed exercise descriptions, equipment use, group size, supervision level, exercise timing, rest periods, intensity, and contextual factors. The study is observational, with no treatments assigned, and aims to provide insights into real-world physiotherapy practices and guideline implementation in Flemish nursing homes.
CONDITIONS
Brief Title
Physiotherapy Practice in Flemish Nursing Homes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Licensed physiotherapist working in a Flemish nursing home
- Willing to participate in the study
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 weeks
Participants are observed during the mapping of therapy sessions provided by physical therapists in Flemish nursing homes.
Observations during routine therapy sessions over 2 weeks
Trial Site Locations
Total: 3 locations
1
Nursing home
Deurne, Antwerpen, Belgium
Not Yet Recruiting
2
Nursing home
Zoersel, Antwerpen, Belgium
Actively Recruiting
3
Nursing home
Tongeren, Limburg, Belgium
Actively Recruiting
Research Team
M
Maxine Claes, Msc
J
Joke Spildooren, Prof.dr
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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