PERFECTED: Caring for Patients With Hip-fracture & Memory Difficulties

Dementia Clinical Trial

— PERFECTED  

Official title:

PERFECTED WP1 P4: A Qualitative Exploration of Lay and Professional Stakeholder Views of Care Delivery in Hospitals for Patients With Hip-fracture & Memory Difficulties

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03308123
• Other study ID #: 15/EE/0007
• Secondary ID: DTC-RP-PG-0311-1
• Status: Completed
• Phase: N/A
• First received: August 9, 2017
• Last updated: October 11, 2017
• Start date: February 1, 2015
• Est. completion date: February 22, 2016

Study information

• Verified date: August 2017
• Source: University of East Anglia
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: February 22, 2016
• Est. primary completion date: July 1, 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• A hip-fracture patient recently discharged (within a month) from an acute hospital in one of the study locations.

• 60 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

Exclusion Criteria:

• Lacks mental capacity

Related Conditions & MeSH terms

• Dementia
• Fractures, Bone
• Hip Fractures

Intervention

Other:
• Observational study, not interventional
Not an intervention study

Locations

Country	Name	City	State
United Kingdom	University of East Anglia	Norwich	Norfolk

Sponsors (1)

Lead Sponsor	Collaborator
University of East Anglia

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Semi-Structure Interview	Stakeholder experiences	1 month