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Completed

NCT Number: NCT02714452

A Person-centred and Thriving Promoting Care Model for Residential Aged Care

The overall aim of this study is to evaluate the effects, meaning and significance of a person-centred and thriving promoting model for residential aged care in Australia, Norway and Sweden. More specifically, the following research questions will be explored:

1. Can a person-centred and thriving promoting care model increase residents' thriving, and have a positive impact on residents' perception of the caring environment? 2. Can a person-centred and thriving promoting care model increase relatives' satisfaction with care, and have a positive impact on their experience of visiting their relative, and perception of the caring environment? 3. Can a person-centred and thriving promoting care model increase staff's job satisfaction, decrease stress of conscience, and have a positive impact on their perception of the caring environment and person-centred care? 4. What meaning and significance do relatives and staff ascribe to the intervention? The study is designed as a multi-centre, controlled group before-after design with participating sites in Victoria (Australia), Oslo (Norway) and Västerbotten (Sweden). Two residential aged care facilities at each site will be allocated to either intervention or control, in total three intervention and three control facilities divided over the three sites.

Care staff at the intervention facilities will participate in a 12-month education on how to integrate aspects of person-centredness, thriving and a caring environment into daily care practice. Participating staff will work together with their colleagues and members from the research group to create a reflective and creative learning environment that builds on and develops the staff members' clinical experience and skills, and combines it with theoretical and research-based knowledge.

At the control facilities, care staff will participate in a 2-hour lecture on the theoretical and philosophical foundations of person-centredness, thriving and a caring environment, and then continue with practice without further involvement from the research team.

Evaluation data will be collected by study specific questionnaires before the education starts, immediately after the education and at a 6-month follow-up. In addition, focus group interviews and individual interviews will be conducted with a selection of staff members and relatives at the intervention facilities to explore meaning and significance of the intervention.

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Key information

Conditions

Aging

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Umeå University

Umeå, SE-90187, Sweden

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • minimum 18 years of age
  • living in the facility for >1 month by the time of data collection
  • visiting the residential aged care facility on a regular basis (>1/month)
  • working in the residential aged care facility on a temporary and or permanent basis (>1month contract)
  • have been working >1 month in the residential aged care facility by the time of data collection.

Exclusion criteria

  • newly moved in to the facility
  • visiting the facility more seldom than once a month
  • working on a short-term contract

Treatment and study plan

Person-centred care

Behavioral

Person-centred and thriving promoting care

Primary outcomes

  1. Change in The Thriving of Older People Assessment Scale between baseline and follow-up

    Time frame: Change from baseline thriving at 12 and 18 months

    Data will be collected from residents at both intervention and control facilities by either self-rating or proxy-rating surveys at baseline and at 12 and 18 months follow-up

  2. Change in relatives' satisfaction with care measured by the Pyramid questionnaire

    Time frame: Change from baseline satisfaction at 12 and 18 months

    Data will be collected from relatives at both intervention and control facilities by self-rating surveys at baseline and at 12 and 18 months follow-up

  3. Change in staff's job satisfaction measured by the The Job satisfaction questionnaire

    Time frame: Change from baseline job satisfaction at 12 and 18 months

    Data will be collected from staff at both intervention and control facilities by self-rating surveys at baseline and at 12 and 18 months follow-up

Secondary outcomes

  1. Change in participants' experience of the caring environment measured by The Person-centred Climate Questionnaire

    Time frame: Change from baseline experience at 12 and 18 months

    Data will be collected from residents, relatives and staff at both intervention and control facilities by either self-rating or proxy-rating surveys at baseline and at 12 and 18 months follow-up

  2. Change in relatives' experienced satisfaction with visiting the nursing home and their relative, measured by Visual Analogue Scales of participants' subjective experiences of 12 statements, ranging from 0 (totally disagree) to 10 (totally agree).

    Time frame: Change from baseline satisfaction at 12 and 18 months

    Data will be collected from relatives at both intervention and control facilities by self-rating surveys at baseline and at 12 and 18 months follow-up. Group level data will be aggregated using mean values of the participants' ratings.

  3. Change in staff's stress of conscience measured by the Stress of Conscience questionnaire

    Time frame: Change from baseline stress of conscience at 12 and 18 months

    Data will be collected from staff at both intervention and control facilities by self-rating surveys at baseline and at 12 and 18 months follow-up

  4. Change in staff's perception of the person-centredness of care measured by the Person-centred Care Assessment Tool

    Time frame: Change from baseline perception at 12 and 18 months

    Data will be collected from staff at both intervention and control facilities by self-rating surveys at baseline and at 12 and 18 months follow-up

Sponsors and collaborators

Lead sponsor

Umeå University

Other

Collaborators

  • La Trobe University
  • University of Oslo

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Mar 21, 2016
Registry last updated
Oct 11, 2018

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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