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Self-Management Behaviors of Caregivers of the Chronically Critically Ill (ASSIST)

Primary Purpose

Critical Illness

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ASSIST
Attention-Control
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Critical Illness focused on measuring caregiver, chronically critically ill

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • aged 18 years or older
  • recognized as the family member who will assume the caregiver role for a critically ill adult requiring at least 72 hours of mechanical ventilation and scheduled for a discharge to an extended care facility
  • speak and comprehend English

Exclusion Criteria:

  • currently practicing mindfulness-based interventions
  • require psychotherapy or required psychotherapy within the last three months
  • have a history of dementia or major neurological illness
  • pregnant
  • history of medical conditions or procedures that is contraindicated for fMRI scanning
  • claustrophobia requiring anxiolytics or sedation
  • expected to relocate from Northeast Ohio within two months

Sites / Locations

  • University Hospitals Case Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

ASSIST

Attention-Control

Arm Description

The ASSIST intervention will deliver daily doses of MMT and vary dose intensity of all components each day based on the subject's biophysical data. Across a 30-day period, the ASSIST intervention will capture and analyze data to deliver on-demand MMT, guided practices to promote sleep hygiene and physical activity. Each day, subjects will receive at least one prompt to practice MMT (about 5 minutes at a time). However, based on the subject's biophysical sensor data, subjects could receive a maximum of 5 alerts or prompts per day from the device to enhance stress reduction, sleep hygiene, or physical activity.

This intervention exposes subjects to the wearable technology without the self-management components to minimize novelty effects. Subjects assigned to this condition will wear the device for 30 days, which offers them an opportunity to experientially learn to self-monitor and employ self-regulatory skills by viewing the display biophysical data. Subjects in this condition will not receive any prompts from the device.

Outcomes

Primary Outcome Measures

Repeated Measures
ANCOVA Model (F-Statistic)

Secondary Outcome Measures

Change in Active Living Protocol (captured on wearable device)
Measure of Caregiver Sleep Activity
Change in Daily Diary of Physical Activity (captured on wearable device)
Measure of Caregiver Physical Activity
Change in Perceived Stress Scale
Measure of Caregiver Stress
Change in PROMIS-29 Scale
Measure of Caregiver Anxiety and Depression
Change in Zarits Burden Interview
Measure of Caregiver Burden
Change in Health Behaviors Questionnaire
Measure of Caregiver Health Related Quality of Life
Change in Heart Rate Variability (captured on wearable device)
Measure of Caregiver Heart Rate Variablity

Full Information

First Posted
February 6, 2017
Last Updated
July 8, 2018
Sponsor
Case Western Reserve University
Collaborators
National Institutes of Health (NIH), National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT03065829
Brief Title
Self-Management Behaviors of Caregivers of the Chronically Critically Ill
Acronym
ASSIST
Official Title
The Mediating Effects of Decentering on Self-Management Behaviors in Caregivers of Critically Chronically Ill Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
February 2016 (Actual)
Primary Completion Date
July 31, 2017 (Actual)
Study Completion Date
July 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
National Institutes of Health (NIH), National Institute of Nursing Research (NINR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
For family members of chronically critically ill (CCI) patients, an ICU admission marks a significant milestone in the patient's illness trajectory that highlights the onset of end of-life issues and an abrupt need for family members to assume the caregiver role for the first time. Assuming the caregiver role can have devastating and longstanding health consequences for family members, which can impair their ability to sustain caregiving behaviors for a CCI patient. The unrelenting psychological distress perceived by caregivers of CCI patients is linked to significant reductions in their self-management and health outcomes. The purpose of this study is to evaluate a theoretically-derived Adaptive SenSor-Based Intervention for Caregiver Self-ManagemenT (ASSIST) intervention compared to an attention control condition for first time caregivers of CCI patients discharged to an extended care facility. One group will be exposed to the ASSIST intervention and will wear the sensor-based technology for 30 days and receive a daily dose of MMT. Biophysical sensor data (blood pressure, heart-rate variability, pedometry, and actigraphy) will be continuously acquired and analyzed using anomaly detection and machine learning techniques to vary the dose intensity (number of doses per day) of the two components of ASSIST adding a real-time, adaptive feature to promote caregiver self-management. The other group will wear the sensor-based technology for 30 days but will not receive the daily dose of MMT. The investigators will randomly assign participants to each group.
Detailed Description
The investigators will conduct a randomized controlled trial to examine the ASSIST intervention compared to an attention control condition among 20 first time caregivers of CCI patients discharged to an extended care facility. The investigators will collect mixed methods data at baseline (T1) on Day 15 (T2) and Day 30 (T3) after subject enrollment to describe changes in proximal and distal outcomes. We have chosen our time points to capture neural and behavioral changes associated with the intervention. The investigators aim to: Determine whether there are differences in the distal outcomes [psychological burden (anxiety, depression, caregiver burden, HRQoL), cardiovascular health (BP and HRV) and economic costs] between subjects who were exposed to ASSIST compared to those exposed to the attention control condition. Examine whether decentering, self-efficacy, decision-making, motivation, caregiver activation, and perceived stress mediate the relationship between exposure to a self-management condition (ASSIST vs. attention control) and the proximal (self-management) outcomes (stress reduction behaviors, sleep hygiene behaviors, and physical activity). Determine if social support and demographics (gender and age) moderate the proximal outcomes [emotional distress, sleep quality, and physical activity] or distal outcomes [psychological burden (anxiety, depression, caregiver burden, HRQoL), cardiovascular health (BP and HRV) and economic costs]. Explore the differences in brain activation (structural and fMRI scans) and HPA function and stress response (hair cortisol, inflammation panel) between subjects exposed to ASSIST compared to those exposed to the attention control condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness
Keywords
caregiver, chronically critically ill

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Our model posits that effective caregiver self-management depends on analytic and emotional processing. The investigators hypothesize the ASSIST intervention will improve analytic processing by improving self-monitoring. ASSIST will expose subjects to mindfulness meditation training and promote self-awareness, which will aid the regulation of their emotional processing and improve proximal outcomes. The investigators expect proximal self-management outcomes to influence the distal outcomes of caregiver health. Our model will also test the mediating effects of decentering, processing, the hypothalamic-pituitary axis (HPA), inflammatory stress response, and cognitive mediators. The influence of potential moderators will be assessed for their effect on the relationship between the self-management intervention and the proximal and distal outcomes.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ASSIST
Arm Type
Experimental
Arm Description
The ASSIST intervention will deliver daily doses of MMT and vary dose intensity of all components each day based on the subject's biophysical data. Across a 30-day period, the ASSIST intervention will capture and analyze data to deliver on-demand MMT, guided practices to promote sleep hygiene and physical activity. Each day, subjects will receive at least one prompt to practice MMT (about 5 minutes at a time). However, based on the subject's biophysical sensor data, subjects could receive a maximum of 5 alerts or prompts per day from the device to enhance stress reduction, sleep hygiene, or physical activity.
Arm Title
Attention-Control
Arm Type
Experimental
Arm Description
This intervention exposes subjects to the wearable technology without the self-management components to minimize novelty effects. Subjects assigned to this condition will wear the device for 30 days, which offers them an opportunity to experientially learn to self-monitor and employ self-regulatory skills by viewing the display biophysical data. Subjects in this condition will not receive any prompts from the device.
Intervention Type
Behavioral
Intervention Name(s)
ASSIST
Intervention Description
Wearable sensor technology delivering mindfulness meditation training (MMT) and health promotion (sleep hygiene and physical activity) .
Intervention Type
Behavioral
Intervention Name(s)
Attention-Control
Intervention Description
Wearable sensor technology only viewing biophysical sensor data.
Primary Outcome Measure Information:
Title
Repeated Measures
Description
ANCOVA Model (F-Statistic)
Time Frame
Baseline to 30 days
Secondary Outcome Measure Information:
Title
Change in Active Living Protocol (captured on wearable device)
Description
Measure of Caregiver Sleep Activity
Time Frame
From Baseline to up to 30 days
Title
Change in Daily Diary of Physical Activity (captured on wearable device)
Description
Measure of Caregiver Physical Activity
Time Frame
From Baseline to up to 30 days
Title
Change in Perceived Stress Scale
Description
Measure of Caregiver Stress
Time Frame
From Baseline to up to 30 days
Title
Change in PROMIS-29 Scale
Description
Measure of Caregiver Anxiety and Depression
Time Frame
From Baseline to up to 30 days
Title
Change in Zarits Burden Interview
Description
Measure of Caregiver Burden
Time Frame
From Baseline to up to 30 days
Title
Change in Health Behaviors Questionnaire
Description
Measure of Caregiver Health Related Quality of Life
Time Frame
From Baseline to up to 30 days
Title
Change in Heart Rate Variability (captured on wearable device)
Description
Measure of Caregiver Heart Rate Variablity
Time Frame
From Baseline to up to 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: aged 18 years or older recognized as the family member who will assume the caregiver role for a critically ill adult requiring at least 72 hours of mechanical ventilation and scheduled for a discharge to an extended care facility speak and comprehend English Exclusion Criteria: currently practicing mindfulness-based interventions require psychotherapy or required psychotherapy within the last three months have a history of dementia or major neurological illness pregnant history of medical conditions or procedures that is contraindicated for fMRI scanning claustrophobia requiring anxiolytics or sedation expected to relocate from Northeast Ohio within two months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald L. Hickman, PhD, RN
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospitals Case Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32205788
Citation
Moore SM, Musil CM, Alder ML, Pignatiello G, Higgins P, Webel A, Wright KD. Building a Research Data Repository for Chronic Condition Self-Management Using Harmonized Data. Nurs Res. 2020 Jul/Aug;69(4):254-263. doi: 10.1097/NNR.0000000000000435.
Results Reference
derived

Learn more about this trial

Self-Management Behaviors of Caregivers of the Chronically Critically Ill

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