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Rehabilitation for Survivors of Out-of-hospital Cardiac Arrest

Primary Purpose

Cardiac Arrest, Heart Arrest, Cardiopulmonary Resuscitation

Status
Recruiting
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Individually tailored rehabilitation intervention
Usual care
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrest focused on measuring Labour marked, Cardiac arrest, Heart Arrest, Cardiopulmonary Resuscitation, Return to work, Return-to-work, Back to Work, Rehabilitation, Recovery of Function, Cardiac Rehabilitation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • ≥18 years of age
  • part of the labor force at the day of enrolling the trial
  • at least two years until qualified to receive retirement state pensions
  • can understand and fulfil the study survey (in Danish).

Exclusion criteria:

  • severe cognitive impairment following the cardiac arrest (i.e. can't be discharged to own home, but require longer (neuro)rehabilitation at higher specialized center),
  • a medical diagnose of dementia, Alzheimer's disease, stroke, or acquired brain injury
  • severe drug abuse (judged by treating physician)
  • severe alcohol abuse (>40 units/week).

Sites / Locations

  • RigshospitaletRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Individually tailored rehabilitation intervention + usual care

Usual care

Arm Description

A comprehensive neurocognitive assessment and a thorough individual assessment of rehabilitation needs will be conducted to inform the individually tailored intervention plan. Core intervention elements are: 1) comprehensive assessment of individual rehabilitation needs including neuropsychology tests in order to make a individually tailored intervention plan coordinated with the multidisciplinary rehabilitation team, 2) providing strategies to lessen impact for the individual cognitive impairment, 3) educating survivors and relatives about the impact of a cardiac arrest and consequences on daily life, 4) work preparation, including establishment of routines and opportunities to practice work skills and 5) collaboration with the local municipality's job centre and employers to plan, support and monitor graded RTW, 6) short term therapy by psychologist dealing with thoughts and behaviour in relation to cardiac arrest.

All participants including those allocated to the usual care group will be seen by an occupational therapist if their MoCA screening score ≤26. Furthermore, if considered relevant by the discharging unit, survivors are referred for rehabilitation provided and delivered in the local municipality where the participant is resident. The content of the rehabilitation will typically be based on the content of the rehabilitation plan from the discharging hospital unit and an individual assessment of the survivors' expressed needs, within the local municipality where the participant is resident.

Outcomes

Primary Outcome Measures

Labour market participation using data from the DREAM database
The primary outcome of the clinical trial is labour market participation, defined as a dichotomized outcome, employment vs. on social transfer payment 12 months after hospital discharge.

Secondary Outcome Measures

Return-to-work - Multi-state models of patients change in states from baseline to 12-months after hospital discharge
3 multi-state models (working full-time, Working part-time, sick leave and the absorbing stated retired). Patients are not very likely to die during follow-up; this state may be superfluous. In the model working hours and retirement to private pensions will need to be assessed using self-reported data.
PRO: Readiness for return-to-work (RRTW)
Readiness for return-to-work (RRTW) consisting of 22 items.
PRO: Degree of return-to-work
Single items covering degree of RTW in hours weekly (compared to prior to the cardiac arrest), job describtion (changed Y/N) and job modification (changes Y/N).
PROM: EQ-5D-5L
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. The EQ VAS records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'. The VAS can be used as a quantitative measure of health outcome that reflect the patient's own judgement.
PROM: Multidimensional fatigue inventory (MFI-20)
The MFI is a 20-item self-report instrument designed to measure fatigue. It covers the following dimensions: general fatigue, physical fatigue, reduced activity, reduced motivation and mental fatigue.
PROM: The Hospital Anxiety and Depression Scale (HADS)
The questionnaire comprises seven questions for anxiety and seven questions for depression
PROM: The Pittsburgh Sleep Quality Index (PSQI)
The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The measure consists of 19 individual items, creating 7 components that produce one global score
The Health Literacy Questionnaire (HLQ)
HLQ has nine scales that each measure an aspect of the multidimensional construct of health literacy.
PROM: Disease specific health-related quality of life (HeartQoL)
The HeartQoL questionnaire comprises 14-items forming a physical, emotional subscales and a global score,
The Impact of Event Scale - Revised (IES-R)
The Impact of Event Scale - Revised (IES-R) measures syptoms related to post-traumatic stress disorder (PTSD) The IES-R has 22 questions, that comprises a total subjective stress scale and three subscales (Intrusion, Avoidance, Hyperarousal)

Full Information

First Posted
November 27, 2021
Last Updated
May 11, 2023
Sponsor
Rigshospitalet, Denmark
Collaborators
Copenhagen University Hospital, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT05173740
Brief Title
Rehabilitation for Survivors of Out-of-hospital Cardiac Arrest
Official Title
The ROCK Trial. A Multidisciplinary Rehabilitation Intervention Targeted Return-to-work in Sudden Out-of-hospital Cardiac Arrest Survivors A Pragmatic Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
Copenhagen University Hospital, Denmark

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
This study is a parallel group multicentre investigator-initiated clinical randomised controlled superiority trial that will include a total of 214 survivors of OHCA. Participants will to be randomized with a 1:1 allocation ratio to either a intervention consisting of a comprehensive initiated tailored rehabilitation intervention focusing on supporting RTW plus usual care compared to usual care alone.
Detailed Description
The ROCK trial is a two-arm multicentre investigator-initiated clinical randomised controlled superiority trial evaluating the effectiveness of a comprehensive individually tailored rehabilitation intervention focusing on supporting labour marked participation of survivors of out-of-hospital cardiac arrest compared to usual care, with primary endpoint measured after 12 months follow-up. The overall aim of the ROCK trial is to evaluate the effectiveness of a comprehensive individually tailored multidisciplinary rehabilitation intervention for survivors of OHCA on RTW compared to usual care. The investigators hypothesize that the intervention will result in a higher-level labour marked attachment one year after hospital discharge in addition to increased health-related quality of life. A full statistical analysis plan describing all details have been developed. In short, data from the national register on social transfer payments (DREAM database) will form the basis for the primary outcome. The primary outcome is labour market participation, defined as the proportion of employment vs. on social transfer payment, and the primary end point will be collected 12 months after hospital discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest, Heart Arrest, Cardiopulmonary Resuscitation, Return to Work, Return-to-work, Rehabilitation, Recovery of Function, Cardiac Rehabilitation
Keywords
Labour marked, Cardiac arrest, Heart Arrest, Cardiopulmonary Resuscitation, Return to work, Return-to-work, Back to Work, Rehabilitation, Recovery of Function, Cardiac Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Before data extraction and data analysis all data will be anonymized, and group allocation will be blinded as (group X and Y). Participants will be randomly assigned to either the intervention or the usual care group using a computer random generator, with a 1:1 allocation. The randomisation will be conducted by a blinded investigator.
Allocation
Randomized
Enrollment
214 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Individually tailored rehabilitation intervention + usual care
Arm Type
Experimental
Arm Description
A comprehensive neurocognitive assessment and a thorough individual assessment of rehabilitation needs will be conducted to inform the individually tailored intervention plan. Core intervention elements are: 1) comprehensive assessment of individual rehabilitation needs including neuropsychology tests in order to make a individually tailored intervention plan coordinated with the multidisciplinary rehabilitation team, 2) providing strategies to lessen impact for the individual cognitive impairment, 3) educating survivors and relatives about the impact of a cardiac arrest and consequences on daily life, 4) work preparation, including establishment of routines and opportunities to practice work skills and 5) collaboration with the local municipality's job centre and employers to plan, support and monitor graded RTW, 6) short term therapy by psychologist dealing with thoughts and behaviour in relation to cardiac arrest.
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
All participants including those allocated to the usual care group will be seen by an occupational therapist if their MoCA screening score ≤26. Furthermore, if considered relevant by the discharging unit, survivors are referred for rehabilitation provided and delivered in the local municipality where the participant is resident. The content of the rehabilitation will typically be based on the content of the rehabilitation plan from the discharging hospital unit and an individual assessment of the survivors' expressed needs, within the local municipality where the participant is resident.
Intervention Type
Other
Intervention Name(s)
Individually tailored rehabilitation intervention
Intervention Description
Individually tailored rehabilitation intervention
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual care
Primary Outcome Measure Information:
Title
Labour market participation using data from the DREAM database
Description
The primary outcome of the clinical trial is labour market participation, defined as a dichotomized outcome, employment vs. on social transfer payment 12 months after hospital discharge.
Time Frame
12-months after hospital discharge
Secondary Outcome Measure Information:
Title
Return-to-work - Multi-state models of patients change in states from baseline to 12-months after hospital discharge
Description
3 multi-state models (working full-time, Working part-time, sick leave and the absorbing stated retired). Patients are not very likely to die during follow-up; this state may be superfluous. In the model working hours and retirement to private pensions will need to be assessed using self-reported data.
Time Frame
12-months after hospital discharge
Title
PRO: Readiness for return-to-work (RRTW)
Description
Readiness for return-to-work (RRTW) consisting of 22 items.
Time Frame
2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PRO: Degree of return-to-work
Description
Single items covering degree of RTW in hours weekly (compared to prior to the cardiac arrest), job describtion (changed Y/N) and job modification (changes Y/N).
Time Frame
2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PROM: EQ-5D-5L
Description
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. The EQ VAS records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'. The VAS can be used as a quantitative measure of health outcome that reflect the patient's own judgement.
Time Frame
Baseline (Hospital discharge), 2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PROM: Multidimensional fatigue inventory (MFI-20)
Description
The MFI is a 20-item self-report instrument designed to measure fatigue. It covers the following dimensions: general fatigue, physical fatigue, reduced activity, reduced motivation and mental fatigue.
Time Frame
Baseline (Hospital discharge), 2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PROM: The Hospital Anxiety and Depression Scale (HADS)
Description
The questionnaire comprises seven questions for anxiety and seven questions for depression
Time Frame
Baseline (Hospital discharge), 2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PROM: The Pittsburgh Sleep Quality Index (PSQI)
Description
The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The measure consists of 19 individual items, creating 7 components that produce one global score
Time Frame
Baseline (Hospital discharge), 2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
The Health Literacy Questionnaire (HLQ)
Description
HLQ has nine scales that each measure an aspect of the multidimensional construct of health literacy.
Time Frame
2 weeks, 26 weeks and 52 weeks after hospital discharge
Title
PROM: Disease specific health-related quality of life (HeartQoL)
Description
The HeartQoL questionnaire comprises 14-items forming a physical, emotional subscales and a global score,
Time Frame
2 weeks, 12 weeks, 26 weeks and 52 weeks after hospital discharge
Title
The Impact of Event Scale - Revised (IES-R)
Description
The Impact of Event Scale - Revised (IES-R) measures syptoms related to post-traumatic stress disorder (PTSD) The IES-R has 22 questions, that comprises a total subjective stress scale and three subscales (Intrusion, Avoidance, Hyperarousal)
Time Frame
12 weeks, 26 weeks and 52 weeks after hospital discharge
Other Pre-specified Outcome Measures:
Title
Montreal Cogntive Assessment (MoCA)
Description
The MoCA is a cognitive screening test designed to assist Health Professionals in the detection of mild cognitive impairment
Time Frame
Baseline (Hospital discharge)
Title
Assessment of Motor and Process Skills (AMPS)
Description
Measures the quality of a person's ADL task performance
Time Frame
Baseline (Hospital discharge)
Title
Neurocognitive testing: Trail Making Test (TMT) Parts A and B
Description
the ability to think, reason, and remember
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: The Wechsler Adult Intelligence Scale
Description
WAIS-IV
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: The Repeatable Battery for the Assessment of Neuropsychological Status
Description
RBANS
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: Rey Complex Figure Test
Description
is a neuropsychological assessment in which examinees are asked to reproduce a complicated line drawing
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: The Symbol Digit Modalities Test (SDMT)
Description
A screening instrument to assess neurological dysfunction
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: The Five-Point Test
Description
The Five-Point Test is a test for measuring figural fluency functions
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: The Kohs Block test
Description
a performance test designed to be an IQ test
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: Animal fluency
Description
Verbal fluency tests are a kind of psychological test in which participants have to produce as many words as possible from a category in a given time
Time Frame
1 month after hospital discharge
Title
Neurocognitive testing: Fluency S-words
Description
Verbal fluency tests are a kind of psychological test in which participants have to produce as many words as possible from a category in a given time
Time Frame
1 month after hospital discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: All adult survivors with first time out-of-hospital cardiac arrest Discharged from the Hospitals will be assessed eligible for inclusion Exclusion criteria: Survivors who prior to the cardiac arrest were not part of the labour force with at least two years until they are qualified to receive retirement state pensions Patients that cannot understand and fulfil the study surveys (in Danish) Patients with short witnessed cardiac arrests with return of spontaneous circulation estimated less than 4 minutes and immediate awakening without ICU treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jan Christensen, PhD
Phone
35453001
Email
fysjan@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jan Christensen, PhD
Organizational Affiliation
Department of Occupational Therapy and Physiotherapy, Rigshospitalet, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet
City
Copenhagen
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Christensen, Senior researcher

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
By contacting the corresponding author and upon reasonable request, de-identified data can be made available for individual participant data meta-analysis.
IPD Sharing Time Frame
After publication of all studies explicit stated in the Statistical Analysis Plan (SAP)
IPD Sharing Access Criteria
By contacting the corresponding author and upon reasonable request, de-identified data can be made available for individual participant data meta-analysis.

Learn more about this trial

Rehabilitation for Survivors of Out-of-hospital Cardiac Arrest

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