PERFECTED: Caring for Patients With Hip-fracture & Memory Difficulties
PERFECTED
PERFECTED WP1 P4: A Qualitative Exploration of Lay and Professional Stakeholder Views of Care Delivery in Hospitals for Patients With Hip-fracture & Memory Difficulties
2 other identifiers
observational
52
1 country
1
Brief Summary
This qualitative study is part of the 5-year long (2013-18) PERFECTED (Peri-operative Enhanced Recovery hip-fracture Care of paTiEnts with Dementia) National Institute for Health Research (NIHR) funded research programme. PERFECTED's overall aim is to develop and pilot an evidence-based intervention to improve the hospital care of patients living with dementia who have fractured their hip. The findings from this particular study will support PERFECTED's other activities by exploring stakeholder (lay and professional) views of the hospital care experiences of hip-fracture patients who are experiencing memory difficulties. Best practices and priorities, including attention to cost-consequences will be explored. Semi-structured interviews will be conducted with 15-30 hip-fracture patients with mild memory difficulties recently discharged from acute hospitals in Norwich, Nottingham and Bradford. Equal attention will be given to those patients discharged directly home and those discharged to community hospitals for further rehabilitation. Interviews will be conducted with 15-30 recognised carers of hip-fracture patients with moderate/severe memory difficulties who have recently been discharged from acute hospitals in the same three regions. Semi-structured interviews will also be carried out with a nominated dementia lead in each region. Finally, in each region, small focus groups, face-to-face or telephone interviews will be conducted, with clinical staff of various grades and professions, hospital managers and with NHS commissioners. This study will enable a range of topics and perspectives to be explored and potential components for PERFECTED's intervention to be identified. As part of PERFECTED's on-going commitment to Public Patient Involvement (PPI), lay researchers will be trained to assist in interviewing recognised carers of hip-fracture patients with moderate/severe memory difficulties. Interviews and focus groups will be recorded, transcribed and analysed thematically. Resulting data will address the pre-defined aims of the current study and feed into findings reported across the whole of Work Package 1 of PERFECTED.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
February 22, 2016
CompletedFirst Submitted
Initial submission to the registry
August 9, 2017
CompletedFirst Posted
Study publicly available on registry
October 12, 2017
CompletedOctober 12, 2017
August 1, 2017
5 months
August 9, 2017
October 11, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Semi-Structure Interview
Stakeholder experiences
1 month
Study Arms (3)
Health Care Professionals
Health care professionals
Carers of hip-fracture patients with moderate/severe
Carers of hip-fracture patients with moderate/severe
Discharged hip-fracture patient with memory difficulty
Discharged hip-fracture patient with memory difficulty
Interventions
Not an intervention study
Eligibility Criteria
Recently discharged (within a month) hip-fracture patients with mild memory difficulties
You may qualify if:
- A hip-fracture patient recently discharged (within a month) from an acute hospital in one of the study locations.
- years or older
- Having some memory difficulties as recognised by a relevant member of their care team - supported by an AMT score of 5-8 if required
- Has the cognitive ability to engage with a research interview as determined by a relevant member of their care team
You may not qualify if:
- Lacks mental capacity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of East Anglia
Norwich, Norfolk, NR4 7TJ, United Kingdom
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
George C Fox
University of East Anglia
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 9, 2017
First Posted
October 12, 2017
Study Start
February 1, 2015
Primary Completion
July 1, 2015
Study Completion
February 22, 2016
Last Updated
October 12, 2017
Record last verified: 2017-08