Skip to content

Intensive Care Unit specific Virtual Reality for family members (ICU-VR-F) of patients in the ICU.

Intensive Care Unit specific Virtual Reality for family members (ICU-VR-F) of patients in the ICU. - ICU-VR for family members

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON52583
Enrollment
160
Registered
2020-12-14
Start date
2021-01-27
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

psychische klachten na IC opname van naaste, kwaliteit van leven post-intensive care syndrome family (PICS-F) PTSD

Interventions

Family members will be randomized, based on the patient that is admitted, into two study groups, multiple family members per patient can be included and will be allocated clustered to the same rando

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: • >= 18 years old • First degree family member (sibling, parent, children), responsible for decision making, or sharing the same household (in absence of next of kin) • Able to understand the Dutch language • In possession of a smartphone/tablet which is compatible to watch the ICU-VR module at home • Signed informed consent

Exclusion criteria

Exclusion criteria: • Lack of a formal home address • Family members of patients with an ICU-LOSS

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the effect of ICU-VR-F on the psychological distress (depression, anxiety and PTSD) and HRQoL in family members of ICU patients up to 6 months after ICU discharge.

Secondary

MeasureTime frame
The secondary endpoint is the understanding of the ICU in family members of ICU patients. Other, explorative endpoints are the perceived stress factors of ICU treatment in family members of ICU patients, and the perspective of family members on the ICU-VR-F intervention.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)