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Tele-based Psychological Emotional Support for Informal CARegivers of COVID-19 Patients in Intensive Care (CO-CarES)

Primary Purpose

Posttraumatic Stress Disorder, Prolonged Grief Disorder, COVID

Status
Active
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Tele-delivered psychological intervention
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Posttraumatic Stress Disorder focused on measuring Informal caregiver, COVID-19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • close relatives or friends of a patient hospitalized in an intensive care or intermediary care wards with COVID-19
  • capable of completing online questionnaires
  • speak Danish sufficiently for a therapeutic dialogue
  • provide informed consent

Exclusion Criteria:

  • suffering from a severe psychiatric disorder (such as schizophrenia) or in ongoing psychotherapeutic treatment for a psychiatric disorder (such as major depression generalized anxiety disorder or others), that cannot be paused
  • unable to complete verbal phone- or videoconferencing calls
  • unable to complete electronic questionnaires

Sites / Locations

  • Skejby Hospital
  • Rigshospitalet
  • Hospitalsenheden Vest, Horsens
  • Hvidovre Hospital
  • Sygehus Lillebælt, Kolding
  • Odense University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tele-delivered psychological intervention

Arm Description

Weekly tele-delivered psychological intervention

Outcomes

Primary Outcome Measures

Recruitment rate
Rate of consent among informed eligible participants
Completion rate
Rates of completion of intervention sessions among participants
Peri-traumatic distress inventory (negative emotions)
Symptoms of peri-traumatic distress, min. score 0, max score 24, higher score corresponds to worse distress
Impact of Events Scale (6 item)
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress
Impact of Events Scale (6 item)
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress
Impact of Events Scale (6 item)
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress

Secondary Outcome Measures

Prolonged Grief-13-scale
Prolonged Grief, scored according to diagnostic criteria for prolonged grief disorder
PROMIS Depression (8 item scale)
Symptoms of depression, min. score 8, max score 40, higher score corresponds to worse symptoms
PROMIS Anxiety (8 item scale)
Symptoms of anxiety, min. score 8, max score 40, higher score corresponds to worse symptoms
Perceived Stress Scale (4 item)
Perceived stress, min. score 0, max score 16, higher score corresponds to worse stress

Full Information

First Posted
May 22, 2020
Last Updated
October 27, 2022
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT04409821
Brief Title
Tele-based Psychological Emotional Support for Informal CARegivers of COVID-19 Patients in Intensive Care
Acronym
CO-CarES
Official Title
COVID-19 Caregiver Emotional Support
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 29, 2020 (Actual)
Primary Completion Date
May 31, 2022 (Actual)
Study Completion Date
February 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

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
The experience of a loved one's stay in a COVID-19 intensive care unit (ICU), either intubated or on respiratory support, forces family caregivers (hereafter 'caregivers') to face core existential fears, such as uncertainty and death. It also poses a serious threat to basic human needs for autonomy, competence, and relatedness, as family caregivers have no control over the illness, and limited prior competence in dealing with critical illness. COVID-19 likely aggravates this experience, as social distancing cuts caregivers off from visiting patients in the ICU, from using their usual social supportive network and the threat of infection extends to caregivers themselves, their children and family. Combined, these extreme circumstances put caregivers in emotional turmoil and in need of psychological support and assistance in managing difficult emotions. ICU caregivers are at risk of developing clinically relevant symptoms of anxiety or posttraumatic stress. During the patient's ICU stay, caregivers experience peri-traumatic distress, such as helplessness, grief, frustration and anger, that may predict later posttraumatic stress disorder (PTSD). Symptoms of anxiety and PTSD may last for months to years after the patient's discharge. Further, caregivers of patients who die in an ICU may be at greater risk of prolonged grief disorder. Supportive interventions may reduce psychological late effects in ICU caregivers, but the primary focus of the majority of interventions has been on communication or surrogate decision making. The CO-CarES study aims to develop and test the feasibility of a tele-delivered psychological intervention to enable caregivers of ICU patients with COVID-19 to better endure the overwhelming uncertainty and emotional strain and reduce the risk of posttraumatic stress and prolonged grief. The study hypothesizes that providing psychological intervention during and after the patients' hospitalization, can decrease peri-traumatic distress during ICU hospitalization and decrease risk of post-traumatic stress, anxiety, depression and perceived stress following discharge, as well as prolonged grief in bereavement. A secondary hypothesis is that changes in emotion regulation mediate effects of the intervention on long-term psychological outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder, Prolonged Grief Disorder, COVID
Keywords
Informal caregiver, COVID-19

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Feasibility study
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tele-delivered psychological intervention
Arm Type
Experimental
Arm Description
Weekly tele-delivered psychological intervention
Intervention Type
Behavioral
Intervention Name(s)
Tele-delivered psychological intervention
Intervention Description
The intervention consists of two (or one, if preferred by caregivers) weekly tele-sessions during the ICU stay, lasting up to 30 minutes, and two sessions in the month after discharge from or death in the ICU. Sessions will be conducted via phone-calls or video-conferencing. Therapists will 1) validate caregivers' subjective experience, 2) normalize and psychoeducate about emotional reactions, and 3) offer emotion regulation drawing on contemporary cognitive treatment packages of decentering, acceptance and emotion tolerance. Sessions for bereaved caregivers will include psycho-education about grief, assessment of risk for adverse outcomes and information about available support, if needed. The intervention will be performed based on an intervention manual. The content of the intervention will be continually adapted and tailored to the needs of the participating caregivers by involving all caregivers in co-creating the intervention trough brief post-session interviews.
Primary Outcome Measure Information:
Title
Recruitment rate
Description
Rate of consent among informed eligible participants
Time Frame
At inclusion
Title
Completion rate
Description
Rates of completion of intervention sessions among participants
Time Frame
During and post-intervention (1 month)
Title
Peri-traumatic distress inventory (negative emotions)
Description
Symptoms of peri-traumatic distress, min. score 0, max score 24, higher score corresponds to worse distress
Time Frame
Pre-post intervention (1 month after discharge/death)
Title
Impact of Events Scale (6 item)
Description
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress
Time Frame
1 month post intervention
Title
Impact of Events Scale (6 item)
Description
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress
Time Frame
6 months post intervention
Title
Impact of Events Scale (6 item)
Description
Posttraumatic stress, min. score 6, max score 24, higher score corresponds to worse distress
Time Frame
12/13 months post intervention
Secondary Outcome Measure Information:
Title
Prolonged Grief-13-scale
Description
Prolonged Grief, scored according to diagnostic criteria for prolonged grief disorder
Time Frame
6 and 13 months
Title
PROMIS Depression (8 item scale)
Description
Symptoms of depression, min. score 8, max score 40, higher score corresponds to worse symptoms
Time Frame
Baseline to 1, 6, and 12/13 months
Title
PROMIS Anxiety (8 item scale)
Description
Symptoms of anxiety, min. score 8, max score 40, higher score corresponds to worse symptoms
Time Frame
Baseline to 1, 6, and 12/13 months
Title
Perceived Stress Scale (4 item)
Description
Perceived stress, min. score 0, max score 16, higher score corresponds to worse stress
Time Frame
Baseline to 1, 6, and 12/13 months
Other Pre-specified Outcome Measures:
Title
Short Penn State Worry Questionnaire (3 items)
Description
Worry, min. score 3, max score 15, higher score corresponds to greater worry
Time Frame
Baseline to 1, 6, and 12/13 months
Title
Brooding subscale of Ruminative Responses Scale
Description
Brooding, min. score 5, max score 20, higher score corresponds to greater brooding/rumination
Time Frame
Baseline to 1, 6, and 12/13 months
Title
Intolerance of uncertainty Scale (2 item)
Description
Intolerance of uncertainty, min score 2, max score 8, greater score indicates greater uncertainty intolerance
Time Frame
Baseline to 1, 6, and 12/13 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: close relatives or friends of a patient hospitalized in an intensive care or intermediary care wards with COVID-19 capable of completing online questionnaires speak Danish sufficiently for a therapeutic dialogue provide informed consent Exclusion Criteria: suffering from a severe psychiatric disorder (such as schizophrenia) or in ongoing psychotherapeutic treatment for a psychiatric disorder (such as major depression generalized anxiety disorder or others), that cannot be paused unable to complete verbal phone- or videoconferencing calls unable to complete electronic questionnaires
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Annika von Heymann, PhD
Organizational Affiliation
Department of Oncology, Rigshospitalet, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Skejby Hospital
City
Aarhus
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Hospitalsenheden Vest, Horsens
City
Horsens
Country
Denmark
Facility Name
Hvidovre Hospital
City
Hvidovre
Country
Denmark
Facility Name
Sygehus Lillebælt, Kolding
City
Kolding
Country
Denmark
Facility Name
Odense University Hospital
City
Odense
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Tele-based Psychological Emotional Support for Informal CARegivers of COVID-19 Patients in Intensive Care

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