A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and Cognitive Impairments in Coping With Challenges
Primary Purpose
Relatives, Health Care Providers, Cognitive Impairment
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
EMBRACE (relatives)
EMBRACE (Health care providers)
Sponsored by
About this trial
This is an interventional supportive care trial for Relatives focused on measuring Relatives, informal carer, family carer, ALS/MND, Cognitive impairment, Palliative rehabilitation, Blended learning, Online support, telehealth, e-learning, Peer-support, Health care providers
Eligibility Criteria
Inclusion Criteria: Relatives
- relatives (spouse or partner) living with a person with ALS and cognitive impairments (rated on the ALS-FTD-Q by the relative, cut-off >22) Able to talk and understand proficient danish referred to the national rehabilitation center for neuromuscular diseases and have had a visit from an als-consultant
Exclusion Criteria:
-
Sites / Locations
- The Danish national Rehabilitation Center for neuromuscular diseases
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
EMBRACE (Relatives)
EMBRACE (Health care providers)
Arm Description
Feasibility test of a new palliative rehabilitation blended learning program for relatives of people with ALS/cognitive impairments
Feasibility test of a new palliative rehabilitation blended learning program health care providers helping people with ALS/cognitive impairments
Outcomes
Primary Outcome Measures
Coping with ALS and cognitive impairments
Framework of Complex Intervention in Health: MRC-guidelines according to acceptability, implementation and integration
Secondary Outcome Measures
Burden
The Zarit Burden Interview (ZBI-22) questionnaires at baseline (Pre and post intervention)
Anxiety and Stress
Hospital Anxiety and Depression Scale (HADS) (Pre and post intervention)
Full Information
NCT ID
NCT04638608
First Posted
November 10, 2020
Last Updated
February 14, 2023
Sponsor
Danish Rehabilitation Centre for Neuromuscular Diseases
1. Study Identification
Unique Protocol Identification Number
NCT04638608
Brief Title
A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and Cognitive Impairments in Coping With Challenges
Official Title
A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and FTD in Coping With Challenges
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
October 31, 2022 (Actual)
Study Completion Date
October 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Danish Rehabilitation Centre for Neuromuscular Diseases
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
A complex intervention study on a palliative rehabilitation blended learning program to support relatives and health care providers of people with ALS and cognitive impairments in coping with challenges.
Detailed Description
The projects concerns tree studies.
Identifying experience-based evidence of relative of deceased people with ALS/cognitive impairments and health care providers (working with these persons) and develop an intervention program.
Developing a palliative rehabilitation blended learning program for relatives of people with ALS and cognitive impairments and for the health care providers.
Feasibility testing of the two palliative rehabilitation blended learning programs for relatives and health care providers.
Though online palliative rehabilitation the intervention aims to support both relatives of people with ALS/cognitive impairments and health care providers in coping with challenges related to the diseases.
The intervention consists of blended learning through online videos and virtual group meetings, where peer-support play an essential role. The videos consists of a psycho education, mindfulness based stress reduction, relationship changes, intimacy, sorrow and grief, control management, planning the future, how to communicate, hope, creating memories, external support offers. Besides the videos and group meetings, the relatives are given the possibility to make Ecomaps and diary reflections.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Relatives, Health Care Providers, Cognitive Impairment, Rehabilitation
Keywords
Relatives, informal carer, family carer, ALS/MND, Cognitive impairment, Palliative rehabilitation, Blended learning, Online support, telehealth, e-learning, Peer-support, Health care providers
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare Provider
Allocation
Non-Randomized
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EMBRACE (Relatives)
Arm Type
Other
Arm Description
Feasibility test of a new palliative rehabilitation blended learning program for relatives of people with ALS/cognitive impairments
Arm Title
EMBRACE (Health care providers)
Arm Type
Other
Arm Description
Feasibility test of a new palliative rehabilitation blended learning program health care providers helping people with ALS/cognitive impairments
Intervention Type
Other
Intervention Name(s)
EMBRACE (relatives)
Intervention Description
Online support program for both relatives
Intervention Type
Other
Intervention Name(s)
EMBRACE (Health care providers)
Intervention Description
Online support program for health care providers
Primary Outcome Measure Information:
Title
Coping with ALS and cognitive impairments
Description
Framework of Complex Intervention in Health: MRC-guidelines according to acceptability, implementation and integration
Time Frame
0-4 month
Secondary Outcome Measure Information:
Title
Burden
Description
The Zarit Burden Interview (ZBI-22) questionnaires at baseline (Pre and post intervention)
Time Frame
0-4 month
Title
Anxiety and Stress
Description
Hospital Anxiety and Depression Scale (HADS) (Pre and post intervention)
Time Frame
0-4 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Relatives
relatives (spouse or partner) living with a person with ALS and cognitive impairments (rated on the ALS-FTD-Q by the relative, cut-off >22) Able to talk and understand proficient danish referred to the national rehabilitation center for neuromuscular diseases and have had a visit from an als-consultant
Exclusion Criteria:
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charlotte Handberg, senior researcher
Organizational Affiliation
The National Rehabilitation Center for Neuromuscular Diseases
Official's Role
Study Chair
Facility Information:
Facility Name
The Danish national Rehabilitation Center for neuromuscular diseases
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35610609
Citation
Olesen LK, la Cour K, With H, Mahoney AF, Handberg C. A cross-sectional evaluation of acceptability of an online palliative rehabilitation program for family caregivers of people with amyotrophic lateral sclerosis and cognitive and behavioral impairments. BMC Health Serv Res. 2022 May 24;22(1):697. doi: 10.1186/s12913-022-07986-4.
Results Reference
derived
PubMed Identifier
35187490
Citation
Olesen LK, la Cour K, With H, Handberg C. Reflections of family caregivers and health professionals on the everyday challenges of caring for persons with amyotrophic lateral sclerosis and cognitive impairments: a qualitative study. Palliat Care Soc Pract. 2022 Feb 15;16:26323524221077702. doi: 10.1177/26323524221077702. eCollection 2022.
Results Reference
derived
Learn more about this trial
A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and Cognitive Impairments in Coping With Challenges
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