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Improving Pain Management in Nursing Homes: a Pilot Study

Identification and Development of Interfaces and Processes to Improve Quality of Life of Residents at Senevita ProQuaS 2- Improving Pain Management in Nursing Homes: a Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03471390
Acronym
ProQuaS
Enrollment
250
Registered
2018-03-20
Start date
2017-10-24
Completion date
2019-03-01
Last updated
2021-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Management

Keywords

Nursing Home

Brief summary

This study aims to improve pain management in Swiss nursing homes by addressing behavior change of the care workers with a multilevel intervention

Detailed description

Pain management in nursing homes often is inadequate despite the availability of evidence- based pain management guidelines. Barriers to pain management in nursing homes occur on several levels including lack of knowledge and negative beliefs towards pain of care workers. For this embedded mixed-methods pilot study a convenience sample of maximum six nursing homes will be recruited. The planned intervention comprises the implementation of pain management policies, training of all care workers in pain assessment and management as well as training and introduction of a facility pain champion. Quantitative outcomes assessed at baseline, after three and six months include self-efficacy and attitudes to pain of care workers, functional interference from pain and pain intensity in residents. Feasibility and acceptability of the intervention and potential barriers to its implementation will be explored in focus groups and interviews.

Interventions

OTHERProQuaS 2 Intervention

Training and implementation of facility pain champions, comprehensive training of all care workers in pain assessment and management, implementation of pain management policies

Sponsors

Senevita AG
CollaboratorUNKNOWN
University of Basel
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

non- randomized incomplete stepped-wedge design

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Care workers: * Registered nurses, licensed practical nurses/certified caregivers, nursing assistants, nurse aides and other care workers from the participating nursing home * Working in direct resident care * Participating care workers have to be employed for at least one month at the data collection * Students, apprentices and interns have to be employed at least six months in total * Speak and understand German * Older than 16 years Residents: * All residents living in a participating nursing home, older than 64 years * Written informed consent to participate in data collection signed by the resident or in case of severe cognitive impairment by his/her legally acceptable representative

Exclusion criteria

Care workers: * Temporary employment for less than six months Residents: * Critical current health status or terminal life situation * Known life expectancy less than 3 months * Short term residents (length of stay \<6 months)

Design outcomes

Primary

MeasureTime frameDescription
Self- efficacy in pain managementChange from baseline to 6 monthsCare workers' self-efficacy in pain management scale * investigator-developed scale based on guide for constructing self-efficacy scales (Bandura 2006) * numeric rating scale ranging from 0 =not confident at all to 100=highly confident * total score will be computed by calculating a mean over single item scores (range: 0-100, higher scores indicating better self-efficacy)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026