Individualised Informal Caregiver Training for Palliative Care at Home

NCT ID: NCT02591693

Last Updated: 2016-06-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-08-31
• Study Completion Date: 2016-04-30

Brief Summary

The purpose of this study is to determine whether a training intervention to improve caregiver confidence for family caregivers of patients with palliative care needs at home, is acceptable to patients and their caregivers.

Detailed Description

Many patients with terminal illnesses rely on friends and family for much of their practical day to day care. These friends and family members often lack the skills and confidence to carry out these tasks and studies have shown that many would want more support. Studies have also shown that many patients feel they are a burden.

This study involves carers receiving training to learn the skills they need to care for their loved one. Adult patients with terminal illnesses, currently receiving care from a specified hospice in the South East of England, who have a friend or family member caring for them at home are eligible to be referred for this study.

The training of the carer will be carried out over three sessions by an Occupational Therapist in the patient's own home.The training will focus on goals that the patient and carer have chosen together.

The carer will be asked to complete before and after questionnaires and some will be asked to take part in interviews to see how they felt about the study.

The potential benefits of this study are to increase carer confidence in caring for their loved one.

The overall aim of this study is to test out the research method to see if patients and carers find this training and the outcome measures acceptable. If they do then the investigators plan to learn from this study to design a larger randomised control trial which would be the best way of knowing for sure whether and in what ways this training is helpful.

Conditions

Palliative Care

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Caregiver Training

Three home visits by a specialist occupational therapist, each lasting 1-2 hours. Assessment and training to confidently achieve up to three goals relating to practical activities of daily living identified by patient and caregiver.

On-going usual care from multi-professional team at hospice.

Group Type: EXPERIMENTAL

Caregiver training

Intervention Type: BEHAVIORAL

Occupational therapy training focuses on improving confidence to manage practical aspects of care in areas of daily life important to patient and caregiver, in which caregiver reports or anticipates low levels of confidence.

Usual Care

On-going usual care from multi-professional team at hospice.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Caregiver training

Occupational therapy training focuses on improving confidence to manage practical aspects of care in areas of daily life important to patient and caregiver, in which caregiver reports or anticipates low levels of confidence.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Patient currently at home, reliant on family/friends (lay carers) some or all of the time to help with practical or personal care.
• The carer is aged 18 years or over.
• The carer and the patient have the capacity to consent to being involved in the study.

Exclusion Criteria

• There is a current plan in place for all care to be provided by paid carers full time.
• The patient currently receiving more than one contact with Hospice Specialist Occupational Therapy or is likely to develop needs requiring more than one contact Hospice Occupational Therapy over the four week study intervention period.
• Patients and carers who are not able to speak or understand adequate English for consent to be obtained, to be able to undertake carer training and to complete the study outcome measures.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Oxford University Hospitals NHS Trust

OTHER

Sponsor Role: collaborator

Oxford Brookes University

OTHER

Sponsor Role: collaborator

University of Southampton

OTHER

Sponsor Role: collaborator

University of Oxford

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bee Wee, MB BCh PhD

Role: STUDY_CHAIR

Oxford University Hospitals NHS Trust and University of Oxford

Locations

Sir Michael Sobell House Hospice

Oxford, Oxfordshire, United Kingdom

Countries

United Kingdom

Other Identifiers

REC number 14/SC/1104

Identifier Type: -

Identifier Source: org_study_id