Assessing the Clinical Effect of Video-Based Training for Family Members on Delirium Care

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00037508

Enrollment

268

Registered

2025-07-21

Start date

2026-06-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

F05

Interventions

Group 1: Intervention group: Patients with upcoming surgical procedure and family members who are able to be present daily. Family members receive structured training on delirium and are encouraged to

Eligibility

Sex/Gender

All

Age

70 Years to No maximum

Inclusion criteria

Inclusion criteria: Clinical Frailty Scale =4, planned surgery (trauma surgery, orthopedic surgery, visceral surgery, urological surgery, gynecological surgery. If not emergency surgery, then surgery duration =1 hour)

Exclusion criteria

Exclusion criteria: Delirium on admission, inability to consent due to insurmountable language barrier (patients and relatives), severe hearing/visual impairment or severe pre-existing dementia (MMSE 24 hours).

Design outcomes

Primary

Measure	Time frame
Incidence of perioperative delirium.	—

Secondary

Measure	Time frame
Duraton of delirium, correct recognition of delirium by family members, adherence of family membersto the study protocol.	—

Countries

Germany

Contacts

Public ContactJohannes Trabert

AGAPLESION MARKUS KRANKENHAUS

johannes.trabert@agaplesion.de00496995335311

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026