Development and Evaluation of the DEA App

Dementia Clinical Trial

— DEA  

Official title:

Development and Evaluation of an Application for Supporting Informal Caregivers of People With Dementia in Their Daily Life

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03819816
• Other study ID #: DEA_APP_2019
• Status: Completed
• Phase: N/A
• Start date: February 1, 2019
• Est. completion date: November 1, 2019

Study information

• Verified date: June 2023
• Source: Medical University of Vienna
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background, current situation, and motivation

According to current estimates, 100,000 people in Austria suffer from various types of dementia. According to forecasts, this number of people will rise to approximately 230,000 by 2050 due to the demographic development and the increase of the prevalence rate. Data from the service statistics show that 85% of dementia patients still live in the community in their homes and informal caregivers, such as relatives, support them. In total, more than 300,000 people care for their relatives in Austria in addition to professional support. However, not only the person affected from dementia suffers from the disease, but also, and often at a higher rate, the informal caregivers. Vice versa, the quality of life of those suffering from dementia is significantly influenced by the caregivers' competences and their strategies for resilience.

Study aim and hypothesis

The aim of this study is to evaluate the usability, acceptance, and effect of an app consisting of three modules that provide multidimensional support for informal caregivers of a person with dementia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: November 1, 2019
• Est. primary completion date: August 1, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• informal caregivers of a person with dementia

• 18 years or older

• enough language skills to participate

• give written and oral informed consent

• have an Android smartphone or tablet (required to use the app).

Exclusion Criteria:

• none

Related Conditions & MeSH terms

• Dementia

Intervention

Other:
• DEA-App
The intervention (DEA) group will receive the newly developed app. DEA will consist of three simultaneous modules that provide multidimensional support for informal caregivers aiming to reduce the caregiver burden: Information module The information module consists of general information on the disease and the care of people suffering from dementia. Activity module The activity module suggests individualized activities and physical fitness exercises by a self-learning algorithm, which supports the caregiver to deliver more targeted and easier care. Communication module If two or more persons are caring for one person with dementia, the communication module provides a networking possibility.
• Standard Information group
The control group will receive a leaflet on some general principles for promoting health and well-being in older adults with dementia.

Locations

Country	Name	City	State
Austria	Medical University of Vienna	Vienna
Austria	University of Applied Sciences FH Campus Wien	Vienna

Sponsors (2)

Lead Sponsor	Collaborator
Valentin Ritschl	FH Campus Wien, University of Applied Sciences

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Burden Scale for Family Caregivers	The Burden Scale for Family Caregivers are rated on a scale from 0 (strongly disagree) to 3 (strongly agree). The score ranges from 0 to 84 points. Higher scores indicate greater caregiver burden	3 month after baseline
Secondary	12-item Short-Form Health Survey	The SF-12 is a shortened version of the 36-item Short Form Health Survey (SF-36). It is developed as an applicable instrument for measuring health-related quality of life.	3 month after baseline
Secondary	Adult carers quality of life questionnaire	The Adult Carer Quality of Life Questionnaire is a simple instrument for use with adult carers. It measures quality of life in eight domains: support for caring,; caring choice,; caring stress,; money matters,; personal growth,; sense of value,; ability to care, and; carer satisfaction.	3 month after baseline