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Benefits of the Involvement of Nurses in Meetings Between Physicians and the Families of Patients in the ICU.

Benefits of the Involvement of Nurses in Meetings Between Physicians and the Families of Patients in the ICU.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01745406
Acronym
NEWS
Enrollment
100
Registered
2012-12-10
Start date
2013-01-31
Completion date
2014-10-31
Last updated
2015-08-07

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

Conditions

Family HADS, Family PTSD, Family Satisfaction, Family Traumatic Dissociation, Healthcaregiver Satisfaction

Brief summary

When a patient is admitted to the ICU this often happens so suddenly that this can create a significant amount of stress and anxiety for family members for several reasons. Firstly, the family does not have a pre existing relationship with the ICU team. Secondly, the urgency of the situation and the technic it requires is often such that minimal information can be given to family members. And finally, as a result of the unpredictability of each patient's condition, it can be difficult to predict outcome for family members. Together, these factors compound the stress and anxiety of family members. This anxiety is natural and it is important for health caregivers to be able to offer the best support possible. A high quality communication provided by structured information given by physicians and nurses as well could improve support to the families and lead to greater satisfaction. Giving information to families during meetings is crucial at 3 moments: at the first day when the patient is admitted, at day 3, weekly and each time important news is given (surgery, deterioration in condition, end-of-life). The purpose of this project is to evaluate if the involvement of nurses during those meetings could improve quality in communication which is assessed by mixed methods. Families and healthcare workers satisfaction will be assessed by qualitative methodology. Family peritraumatic stress, symptoms of anxiety and depression and PTSD will be assessed using validated scales. Training of healthcare workers will be done by role play. Information to the families is delivered using a framework for physicians and nurses. All the meetings of the study will be audited by a psychologist.

Detailed description

-Randomized trial with two arms: arm 1: information is delivered by a team (physician and nurse) arm 2: information is delivered by the physician alone -During the different meetings of the study: at day 1, at day 3, weekly and in case of deterioration of the patient condition. The other days, family information is delivered as usually in both arms.

Interventions

None listed

Sponsors

Fondation de France
CollaboratorOTHER
French Society for Intensive Care
CollaboratorOTHER
Fondation Hôpital Saint-Joseph
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. patient : adult, 1 relative at minimum, mechanically ventilated at least 48 hours; and 2. family : french-speaking, adult;

Exclusion criteria

* Conflict, organ donor, refusal to participate.

Design outcomes

Primary

MeasureTime frame
Family satisfaction assessed by qualitative approachPatient's ICU discharge day (up to 3 months after Day 1)

Secondary

MeasureTime frame
Healthcaregivers' satifaction assessed by qualitative approachEnd of the study (up to 2 years)

Other

MeasureTime frame
Family PTSD3 months after patient's ICU discharge (up to 6 months after Day 1)
Family HADS3 months after patient's ICU discharge (up to 6 months after Day 1)
Family peri-traumatic dissociationPatient's ICU discharge (up to 3 months after Day 1)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026