Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID05308862

Prevention of Pressure Ulcers, Malnutrition, Poor Oral Health and Falls Among Older Persons Receiving Municipal Health Care and Registered in the Senior Alert Quality Registry

Led by Malmö University · Updated on 2025-05-09

330

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

M

Malmö University

Lead Sponsor

M

Malmö City

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating an intervention aimed at reducing the risk of pressure ulcers, malnutrition, poor oral health, and falls among older adults living in nursing homes who are registered in the Senior Alert quality registry. The study involves nurse aides, registered nurses, and managers working in these nursing homes to improve preventive care processes and outcomes. This interventional study uses cluster randomization to compare the new intervention to usual care. The study includes two parts: workshops and intervention testing. Groups of nurse aides, registered nurses, and managers from nursing homes assigned to the intervention group participate in workshops designed to develop a prevention intervention together with the research team. These workshops focus on discussing current challenges, improving preventive care routines, and designing the intervention components, which may include tools, educational support, and new ways of working. Nursing homes in the control group continue with their regular care practices. The intervention's feasibility and impact will be assessed through data collection and analysis. Participants' involvement includes data extraction from the Senior Alert registry on risk assessments and preventive care interventions for falls, pressure ulcers, malnutrition, and oral health at baseline (six months prior) and at one, six, and twelve months after the intervention. Additionally, all nurse aides and registered nurses in participating nursing homes will complete questionnaires on job satisfaction, stress, and conscience stress before and six months after the intervention. Background data such as age, gender, work experience, and education will also be collected. Data analysis will compare outcomes between intervention and control groups to evaluate the intervention's effects.

CONDITIONS

Brief 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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Nursing homes registering in Senior Alert, which is a national quality registry
Not Eligible

You will not qualify if you...

  • Not meeting inclusion criteria

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Workshops and Intervention Development

Duration - Several weeks during the intervention preparation phase

Participants in the intervention group attend workshops with nurse aides, registered nurses, and managers to develop and plan a preventive care intervention focused on reducing risks of pressure ulcers, malnutrition, poor oral health, and falls among older persons in nursing homes.

4 to 5 workshop sessions

Intervention Testing

Duration - At least 6 months

Participants in the intervention group test the developed preventive care intervention focusing on improving risk assessments, care interventions, and preventive care processes in nursing homes.

Ongoing participation with no specific visit schedule

Data Collection and Evaluation

Duration - Up to 12 months including 6 months prior to and 6 months after the intervention

Data on risk assessments, preventive care interventions, and participant questionnaires regarding job satisfaction and stress are collected before and after the intervention to evaluate its effectiveness.

Questionnaires at baseline and 6 months after intervention; registry data extraction at baseline, 1 month, and 6 months post-intervention

Trial Site Locations

Total: 1 location

1

Malin Axelsson

Malmö, Sweden, 205 06

Actively Recruiting

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Research Team

M

Malin Axelsson, Phd

C

Christine Kumlien, Phd

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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Published Research Related To This Trial

The STAIR OF KNOWLEDGE-a codesigned intervention to prevent pressure ulcers, malnutrition, poor oral health and falls among older persons in nursing homes in Sweden: development of a complex intervention.

Merita Neziraj, Malin Axelsson, Christine Kumlien...

https://pubmed.ncbi.nlm.nih.gov/37562934