Actively Recruiting
PROSENIOR. Prevention of Pressure Ulcers, Malnutrition, Poor Oral Health and Falls Among Older Persons Receiving Municipal Health Care and Are Registered in the Quality Registry Senior Alert
Led by Malmö University · Updated on 2025-05-09
330
Participants Needed
1
Research Sites
206 weeks
Total Duration
On this page
Sponsors
M
Malmö University
Lead Sponsor
M
Malmö City
Collaborating Sponsor
AI-Summary
What this Trial Is About
Inclusion criteria for study I and II is nurse aides, registered nurses and managers working in nursing homes who register in Senior Alert. To develop an intervention aiming to reduce the risk of pressure ulcers, malnutrition, poor oral health and falls among older persons in nursing homes, workshops will be conducted in collaboration with nurse aides, registered nurses and managers (study I). Cluster randomization is going to take place via a computerized program prior to the workshops meaning that only those nurse aides, registered nurses and managers working in nursing homes allocated to the intervention group are going to develop an intervention together with the research group and then test it (study II). The remaining nurse aides, registered nurses and managers working in nursing homes in the control group continue with regular care.
CONDITIONS
Official Title
PROSENIOR. Prevention of Pressure Ulcers, Malnutrition, Poor Oral Health and Falls Among Older Persons Receiving Municipal Health Care and Are Registered in the Quality Registry Senior Alert
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Nursing homes registered in the Senior Alert national quality registry
You will not qualify if you...
- Not meeting the inclusion criteria of nursing homes registered in Senior Alert
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Malin Axelsson
Malmö, Sweden, 205 06
Actively Recruiting
Research Team
M
Malin Axelsson, Phd
CONTACT
C
Christine Kumlien, Phd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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