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A randomized controlled trial of geriatric liaison intervention in frail surgical oncology patients

A randomized controlled trial of geriatric liaison intervention in frail surgical oncology patients - geriatric intervention

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON30407
Enrollment
294
Registered
2006-12-13
Start date
2007-01-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

cancer in the elderly

Interventions

Intervention: The intervention entails participation of a geriatric nurse and geriatrician in the perioperative treatment of the oncogeriatric surgical patient.

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: frail elderly patients in need for a cancer operation

Exclusion criteria

Exclusion criteria: unable to comply outcome questionaires no compiance for follow-up

Design outcomes

Primary

MeasureTime frame
Main study parameters/endpoints: The main endpoint is the cumulative incidence of delirium (measured with the Delirium Observation Scale and the DSM IV criteria) up to 10 days postoperatively. Secondary endpoints are: returning to the pre-operative living situation within 3 months postoperatively,the Physical Component Summary measure (PCS) of the SF-36, the Mental Component Summary measure (MCS) of the SF-36, complications during hospital stay including mortality, care Dependence Scale at discharge. Direct health care and non-health care costs will be used as economic indicators

Secondary

MeasureTime frame
see above

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)