Clinical Trials Directory

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UnknownNCT06483958

Palliative Care Protocol for Adult Patients Hospitalized in Critical Care Units.

Palliative Care Protocol for Adult Patients at High Risk of Death in Critical Care Units: A Multicentric Stepped Wedge Cluster Randomised Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
248 (estimated)
Sponsor
University of Chile · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to determine the effectiveness of a palliative care protocol in improving the quality of care of adult patients at high risk of dying hospitalized in the critical care unit. Assessing symptom burden (dyspnea, pain and/or anxiety/agitation) until death or day 5 (whichever comes first) Researchers will compare the impact of the palliative care protocol with standard care to see if it improves the quality of care. Participants will: 1. Symptom management. 2. Respect for the autonomy of the patient and his/her family environment. 3. Respectful management of clinical information. 4. Provision of holistic care and support.

Detailed description

We designed a stepped wedge cluster randomized trial The study is implementation in 5 Chilean hospitals, admitting 248 patients. Pre-intervention (control): The practices of each ICU will be maintained, until the moment that according to randomization corresponds the beginning of the intervention, in each center. Post-intervention: Palliative care protocol to improve the quality of care

Conditions

Interventions

TypeNameDescription
BEHAVIORALpalliative care protocol1. Symptom management 2. Respect for patient and family autonomy. 3. Respectful management of clinical information. 4. Provision of holistic care and support.

Timeline

Start date
2024-01-02
Primary completion
2025-07-31
Completion
2025-12-30
First posted
2024-07-03
Last updated
2024-07-03

Locations

1 site across 1 country: Chile

Source: ClinicalTrials.gov record NCT06483958. Inclusion in this directory is not an endorsement.