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The effects of the National Quality Improvement Program Palliative Care

The effectivensess of the National Quality Improvement Program Palliative Care on the number of patients that die at the preferred place, the patients’ and family’s experienced control regarding end-of-life care, the patients’ and family’s experienced coordination of end-of-life care, the patients’ and family’s experienced concordant care with their needs, preferences and values, and the number of patients and families that receive care for their needs in the physical, psychosocial, and spiritual domains

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26353
Enrollment
510
Registered
2013-07-22
Start date
2013-02-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

palliative care

Interventions

National Quality Improvement Program Palliative Care. Implementing 'good pracitces'
• PaTz – a systematic approach to improve the quality and organization of care by timely identification of patients in need of palliative care and by drafting an advance care plan. (Dutch equivalent o

Sponsors

NIVEL, Netherlands institute for health services research.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria for patients are; • Adult patients (18 years and older) • Patient has a life expectancy of less than 6 months, measured by the surprise question, and/or undergoes palliative treatment, such as palliative chemotherapy, palliative radiotherapy, palliative surgery, or other treatments that aim to improve the quality of life and/or to extend life, but do not aim to cure the disease • Patient is physically and mentally capable to respond to questionnaires and to understand Dutch. Inclusion criteria for bereaved relatives are; • Adult person (18 years and older) • Has been a contact person (first contact person) of a deceased patient and has been involved in the care of the deceased patient who died after a sickbed • The decease of the patient has been no shorter than 6 weeks ago and not longer than 6 months ago.

Exclusion criteria

Exclusion criteria: Exclusion criteria for patients are; • Comatose, deeply sedated, or dying patients • Patients who have a care relationship shorter than one week Exclusion criteria for bereaved relatives are; • A contact person of a patient who died suddenly and unexpected.

Design outcomes

Primary

MeasureTime frame
Quality indicators palliative care: a. the number of patients that die at the preferred place b. the patients’ and family’s experienced control regarding end-of-life care c. the patients’ and family’s experienced coordination of end-of-life care d. the patients’ and family’s experienced concordant care with their needs, preferences and values e. the number of patients and families that receive care for their needs in the physical, psychosocial, and spiritual domains

Secondary

MeasureTime frame
2. a. In which way and to what extent are the good practices implemented? b. What are barriers and facilitators of the implementation of the good practices and what are the realised conditions for future sustainability of the ‘good practices’? c. Are implementation processes realised as planned beforehand? 3. What other factors might have influenced the measured effects within the organisations?

Contacts

Public ContactN.J.H. Raijmakers

University Medical Center Utrecht (UMCU), Department of Orthopaedics, P.O. Box 85500

n.j.h.raijmakers@chir.azu.nl+31 (0)30 2506972

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)