INSPIRE study: INvestigating Social and PractIcal suppoRts at the End of life.
- Conditions
- Palliative and end of life care.Not ApplicablePalliative and end of life care
- Registration Number
- ISRCTN18400594
- Lead Sponsor
- Dr Kathleen McLoughlin
- Brief Summary
2015 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/26603516
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 80
Community dwelling adults (over 18 years) living with a life-limiting illness in Limerick, considered by a member of the primary care / hospice at home team to be in their last year of life and/or their carer are eligible to participate in this study. Those who meet the criteria on the brief screening tool as having unmet social / practical needs are eligible for inclusion in the RCT.
In the event that a person with a life limiting illness is not able to engage in the study, as indicated by the nurse responsible for their care, due to their condition or a cognitive impairment, data will not be collected from them directly, but their carer will instead be given the option to engage and complete measures relevant to them.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of the intervention on Instrumental Activities of Daily Living (IADLs) after eight weeks.
- Secondary Outcome Measures
Name Time Method Effect of the intervention on quality of life, social connectedness, psychosocial wellbeing, unscheduled health service utilisation, caregiver burden, adverse impacts, and satisfaction with intervention after eight weeks.