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Cardiopulmonary Resuscitation Witnessing by a Relative

Interest for a Relative of Seeing Himself Proposing to Witness Resuscitation of a Family Member Victim of a Cardiac Arrest

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01009606
Acronym
PRESENCE
Enrollment
570
Registered
2009-11-09
Start date
2009-11-30
Completion date
2011-12-31
Last updated
2013-01-18

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

Conditions

Cardiac Arrest

Keywords

Out-of-hospital, Emergency, Cardiac arrest, Post-traumatic stress disorder

Brief summary

The bereavement generated by the loss of a family member can induce pathological situations: depressive state, anxiety, post-traumatic stress disorder and complicated grief. These morbid factors can be influenced by the death circumstances and in particular by the possibility given to the family to attend the medical management of the patient. This clinical trial aims to evaluate the psychological consequences of bereavement on the relatives according to the possibility of witnessing the cardiopulmonary resuscitation of a family member. This possibility lies within the scope of a strategy of global management of the relatives.

Detailed description

This clinical trial aims to compare the presence of post-traumatic stress disorder on a relative related to the death of a family member: Test group: the medical team will propose to the relative to witness the cardiopulmonary resuscitation. Control group: the medical team will not modify its usual management of care.

Interventions

Usual strategy

Proposition to a relative to witness the cardiopulmonary resuscitation of a family member and debriefing ot the situation

Sponsors

Ministry of Health, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient victim of a cardiac arrest and resuscitation initiated * Occurrence of cardiac arrest at home * Presence of a relative : * husband or spouse * father or mother * son or daughter * brother or sister * Patient's age ≥ 18 years * Relative's age ≥ 18 years * Consent of the relative to the participation in the study

Exclusion criteria

* No understanding of the explanations (language problem, important agitation) * Non-affiliated to social security

Design outcomes

Primary

MeasureTime frame
Percentage of relatives having a score of the Impact of Events Scale (IES) > 303 months

Secondary

MeasureTime frame
Psychological follow-up3 months
Suicide3 and 12 months
Psychological questionnaires as the hospital anxiety and depression scale (HAD), the Mini International Neuropsychiatric Interview (MINI), the Inventory of Complicated Grief (ICG)3 and 12 months
Quality of the cardiopulmonary resuscitationday 0
Questionnaire evaluating the stress of the medical and paramedical teamday 0
Medico-legal recourse12 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026