Improvement of Support to Caregivers of Patients in Specialized Palliative Care at Home

NCT03466580 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 466

Last updated 2021-01-27

No results posted yet for this study

Summary

The aim of the project is to evaluate the use of the caregiver-led 'CSNAT intervention' to identify, prioritize and address support needs among caregivers of patients who are starting in specialized palliative care at home in Denmark

Conditions

  • Palliative Care

Interventions

BEHAVIORAL

The Carer Support Needs Assessment Tool (CSNAT) intervention

The CSNAT intervention is a caregiver-led approach where the caregiver first identifies his/her needs of support in the CSNAT, which consists of 14 support domains. Then the practitioner facilitates the intervention where the caregiver prioritizes which domains to discuss. In the conversation, the caregiver's domain priorities and subsequently identified support needs are discussed with the practitioner to agree on actions/solutions and a shared action plan. The intervention will be offered each caregiver twice: the first time between 0 and 13 days after enrollment, and the second time between 15 and 27 days after enrollment.

Sponsors & Collaborators

  • Danish Cancer Society

    collaborator OTHER
  • The A.P. Moeller Foundation

    collaborator UNKNOWN
  • The Palliative Unit, Amager-Hvidovre Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • Arresoedal Hospice

    collaborator UNKNOWN
  • Diakonissestiftelsens Hospice

    collaborator UNKNOWN
  • Hospice Soendergaard

    collaborator UNKNOWN
  • Nordsjaellands Hospital

    collaborator OTHER
  • The Palliative Team NORTH, University Hospital Sjaelland

    collaborator OTHER
  • Soenderjylland Hospital

    collaborator UNKNOWN
  • Bispebjerg Hospital

    lead OTHER

Principal Investigators

  • Mogens Groenvold, DMSc PhD MD · Bispebjerg Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-15
Primary Completion
2019-07-31
Completion
2019-12-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03466580 on ClinicalTrials.gov