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ARTIS: Activating Relatives To get Involved in care after Surgery

ARTIS: Activating Relatives To get Involved in care after Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20346
Enrollment
488
Registered
2018-11-08
Start date
2019-04-26
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

Family-centered care, fundamentals of care, surgery, oncology Familiegecentreerde zorg, basiszorg, chirurgie, oncologie

Interventions

Sponsors

Amsterdam UMC, location AMC, Amsterdam, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age equal or above 18 years; • Scheduled for major surgery as treatment for the following indications: premalignant or malignant pancreatic, esophageal or colorectal tumor • An expected hospital stay of at least 5 days postoperatively; • Presence of a suitable family caregiver who is up to deliver basic care during hospitalization and after discharge (if needed) • Presence of a suitable family caregiver who is able to be present during hospitalization (minimum of 8 hours per day) during the first 5 days on the nursing ward.

Exclusion criteria

Exclusion criteria: Patients: • Patients who are expected to remain in the intensive care unit (ICU) for over 72 hours after surgery • Patients who will be operated in another hospital not participating in this study • Patients unable to provide informed consent • Patients who are unable to communicate in Dutch Family caregivers: • Family caregivers with an age equal or below 17 years • Family caregivers who are not able to be present during hospitalization (minimum of 8 hours per day) during the first 5 postoperative days on the nursing ward • Family caregivers who are not nominated as appointed family caregiver by patient • Family caregivers who receive support from healthcare professionals to carry out self-care activities by

Design outcomes

Primary

MeasureTime frame
Primary outcome measure is the number of first unplanned readmissions within 30 days after discharge.

Secondary

MeasureTime frame
Secondary outcomes are postoperative complications, patients¡¯ quality of life, satisfaction of patients with care, unplanned readmissions caused by complications sensible to basic care activities, healthcare costs, amount of home care after discharge, hospital length of stay, sleep quality, anxiety and depression .

Contacts

Public ContactAnne Eskes

Amsterdam UMC

a.m.eskes@amsterdamumc.nl0031205664565

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)