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Completed

NCT Number: NCT03471390

Improving Pain Management in Nursing Homes: a Pilot Study

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

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Senevita Obstgarten, Affoltern am Albis, Switzerland

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

ProQuaS 2 Intervention

Other

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

Primary outcomes

  1. Self- efficacy in pain management

    Time frame: Change from baseline to 6 months

    Care 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)

Sponsors and collaborators

Lead sponsor

University of Basel

Other

Collaborators

  • Senevita AG

Registry information

Official study title

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

Acronym: ProQuaS

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Mar 20, 2018
Registry last updated
Apr 30, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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