Liberalization of Visiting Policies in ICU for Reducing High Risk of Post-traumatic Stress Disorder (OPEN-UNIT)
Primary Purpose
PTSD in Family Members of ICU Patients
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Visiting policies: 24 hours a day, 7 days a week
Restriction of visiting policies < 6 hours
Sponsored by
About this trial
This is an interventional prevention trial for PTSD in Family Members of ICU Patients focused on measuring Posttraumatic stress disorder (PTSD), ICU, visiting hours policies
Eligibility Criteria
Inclusion criteria :
Patient and family member > 18 years or older,
- mechanical ventilation expected for more than 48 h and inclusion between day 3 and 5 from the beginning of mechanical ventilation,
- patient having a family member speaking and understanding French, and with the ability to visit his/her relative during the ICU stay,
- patient and his/her relative consenting to participate in the study, or obtention of family consent in case of patient incompetency
Exclusion criteria :
- Patient without family available or family not speaking or understanding French"
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Visiting policies: open 24h/24
Restriction of visiting policies
Arm Description
Visiting policies: 24 hours a day, 7 days a week
Restriction of visiting policies < 6 hours
Outcomes
Primary Outcome Measures
Symptoms related to posttraumatic stress disorder (PTSD)
Impact event scale (IES). The Impact of Event scale (IES), which assesses symptoms related to post-traumatic stress disorder (PTSD); scores range from 0 (no PTSD-related symptoms) to 75 (severe PTSD-related symptoms).
Secondary Outcome Measures
Beliefs and attitudes of healthcare workers toward visiting hours
Beliefs and Attitudes toward Visitation in ICU Questionnaire (BAVIQ). Beliefs and attitudes of ICU staff members were recorded at the beginning of period 1 (observation period) and at the end of period 2 (intervention period) using a questionnaire named the Beliefs and Attitudes toward Visitation in ICU Questionnaire (BAVIQ). The "Beliefs" questionnaire contains both positively and negatively formulated questions. To calculate an overall score for nurses 'beliefs, we recoded the responses on the negatively formulated questions. Subsequently, we computed the average score over all the belief items. A score of zero corresponded with beliefs that are strongly opposed to open visitation and a score of 4 corresponded with beliefs that are strongly in favor of open visitation.
Family member's needs
Critical Care Family Needs Inventory (CCFNI) Family needs and satisfaction was measured by a modified version of the Critical Care Family Needs Inventory (CCFNI). The satisfaction score was calculated as the sum of the scores on all items; the smallest possible score was 0 (extreme dissatisfaction) and the highest possible score was 14 (extreme satisfaction).
Family members' symptoms of anxiety and depression
Hospital and Anxiety Depression Scale (HADS) The Hospital and Anxiety and Depression Scale (HADS), subscale scores range from 0 (no distress) to 21 (severe distress), HADS subscales scores 5Anxiety and Depression) above 8 were considered to indicate clinically significant symptoms of anxiety or depression.
the proportion of family members with High risk of PTSD occurrence
Score IES > 30 points
Patients' symptoms of anxiety and depression
Hospital and Anxiety Depression Scale (HADS) The Hospital and Anxiety and Depression Scale (HADS), subscale scores range from 0 (no distress) to 21 (severe distress), HADS subscales scores (Anxiety and Depression) above 8 were considered to indicate clinically significant symptoms of anxiety or depression.
the proportion of patients with High risk of PTSD occurrence
Score IES > 30 points
Full Information
NCT ID
NCT03846323
First Posted
December 6, 2018
Last Updated
February 18, 2019
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT03846323
Brief Title
Liberalization of Visiting Policies in ICU for Reducing High Risk of Post-traumatic Stress Disorder
Acronym
OPEN-UNIT
Official Title
Liberalization of Visiting Policies in ICU for Reducing High Risk of Post-traumatic Stress Disorder (PTSD) in Family Members.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
April 18, 2009 (Actual)
Primary Completion Date
December 17, 2013 (Actual)
Study Completion Date
February 12, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This was a cluster randomized study of an ICU level intervention to reduce high risk of post-traumatic stress disorder (PTSD) in family members of ICU patients.
Participating ICUs had restrictive visiting policies (i.e., <6 hours/day) before randomization.
After an observational period and a washout period, participating ICUs were randomized either to maintain their visiting policies or to liberalize their visiting policies (24 hours a day, 7 days a week.)
Detailed Description
Family members of ICU patients are particularly exposed to anxiety, depressive, acute stress disorder, and posttraumatic stress disorder symptoms (PTSD).
It is currently unknown what type of interventions/ strategies to cope with postintensive care syndrome family would produce the best improvement. Experts suggest that symptoms in family members are potentially amenable to intervention by ICU staff. One intervention to reduce PTSD could be a liberalization of the visiting hours. However, restrictions on visiting hours in the intensive care unit (ICU) are usually adopted worldwide.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PTSD in Family Members of ICU Patients
Keywords
Posttraumatic stress disorder (PTSD), ICU, visiting hours policies
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1289 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Visiting policies: open 24h/24
Arm Type
Experimental
Arm Description
Visiting policies: 24 hours a day, 7 days a week
Arm Title
Restriction of visiting policies
Arm Type
Other
Arm Description
Restriction of visiting policies < 6 hours
Intervention Type
Other
Intervention Name(s)
Visiting policies: 24 hours a day, 7 days a week
Intervention Type
Other
Intervention Name(s)
Restriction of visiting policies < 6 hours
Primary Outcome Measure Information:
Title
Symptoms related to posttraumatic stress disorder (PTSD)
Description
Impact event scale (IES). The Impact of Event scale (IES), which assesses symptoms related to post-traumatic stress disorder (PTSD); scores range from 0 (no PTSD-related symptoms) to 75 (severe PTSD-related symptoms).
Time Frame
at day-90 from patient's ICU discharge
Secondary Outcome Measure Information:
Title
Beliefs and attitudes of healthcare workers toward visiting hours
Description
Beliefs and Attitudes toward Visitation in ICU Questionnaire (BAVIQ). Beliefs and attitudes of ICU staff members were recorded at the beginning of period 1 (observation period) and at the end of period 2 (intervention period) using a questionnaire named the Beliefs and Attitudes toward Visitation in ICU Questionnaire (BAVIQ). The "Beliefs" questionnaire contains both positively and negatively formulated questions. To calculate an overall score for nurses 'beliefs, we recoded the responses on the negatively formulated questions. Subsequently, we computed the average score over all the belief items. A score of zero corresponded with beliefs that are strongly opposed to open visitation and a score of 4 corresponded with beliefs that are strongly in favor of open visitation.
Time Frame
120 days
Title
Family member's needs
Description
Critical Care Family Needs Inventory (CCFNI) Family needs and satisfaction was measured by a modified version of the Critical Care Family Needs Inventory (CCFNI). The satisfaction score was calculated as the sum of the scores on all items; the smallest possible score was 0 (extreme dissatisfaction) and the highest possible score was 14 (extreme satisfaction).
Time Frame
At inclusion
Title
Family members' symptoms of anxiety and depression
Description
Hospital and Anxiety Depression Scale (HADS) The Hospital and Anxiety and Depression Scale (HADS), subscale scores range from 0 (no distress) to 21 (severe distress), HADS subscales scores 5Anxiety and Depression) above 8 were considered to indicate clinically significant symptoms of anxiety or depression.
Time Frame
At inclusion and Day-90 from patient's ICU discharge
Title
the proportion of family members with High risk of PTSD occurrence
Description
Score IES > 30 points
Time Frame
At day-90 from patients'ICU discharge
Title
Patients' symptoms of anxiety and depression
Description
Hospital and Anxiety Depression Scale (HADS) The Hospital and Anxiety and Depression Scale (HADS), subscale scores range from 0 (no distress) to 21 (severe distress), HADS subscales scores (Anxiety and Depression) above 8 were considered to indicate clinically significant symptoms of anxiety or depression.
Time Frame
At day-90 from patients'ICU discharge
Title
the proportion of patients with High risk of PTSD occurrence
Description
Score IES > 30 points
Time Frame
At day-90 from patients'ICU discharge
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria :
Patient and family member > 18 years or older,
mechanical ventilation expected for more than 48 h and inclusion between day 3 and 5 from the beginning of mechanical ventilation,
patient having a family member speaking and understanding French, and with the ability to visit his/her relative during the ICU stay,
patient and his/her relative consenting to participate in the study, or obtention of family consent in case of patient incompetency
Exclusion criteria :
- Patient without family available or family not speaking or understanding French"
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
LILA BOUADMA
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Liberalization of Visiting Policies in ICU for Reducing High Risk of Post-traumatic Stress Disorder
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