Skip to main content
OpenTrials
Completed

NCT Number: NCT04638608

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Danish national Rehabilitation Center for neuromuscular diseases

Aarhus, 8000, Denmark

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

-

Treatment and study plan

EMBRACE (relatives)

Other

Online support program for both relatives

EMBRACE (Health care providers)

Other

Online support program for health care providers

Primary outcomes

  1. Coping with ALS and cognitive impairments

    Time frame: 0-4 month

    Framework of Complex Intervention in Health: MRC-guidelines according to acceptability, implementation and integration

Secondary outcomes

  1. Burden

    Time frame: 0-4 month

    The Zarit Burden Interview (ZBI-22) questionnaires at baseline (Pre and post intervention)

  2. Anxiety and Stress

    Time frame: 0-4 month

    Hospital Anxiety and Depression Scale (HADS) (Pre and post intervention)

Sponsors and collaborators

Lead sponsor

Danish Rehabilitation Centre for Neuromuscular Diseases

Other

Registry information

Official study 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

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Nov 20, 2020
Registry last updated
Feb 16, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.