search
Back to results

Viamigo for People With Dementia and Their Informal Caregivers

Primary Purpose

Dementia

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Viamigo
Sponsored by
Maastricht University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dementia focused on measuring social participation, community, technology, mobile application, feasibility

Eligibility Criteria

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

Inclusion Criteria people with dementia: Capacity to give informed consent; Diagnosis of mild to moderate dementia as evaluated by a healthcare professional and as reported by the person with dementia and the informal caregiver (by asking when and where the person has been diagnosed and by who); Living in the community (alone or with family/roommate(s)/friends); Taking part in social activities outside the home; Availability of an informal caregiver who is interested to take part in this study; Having an Android smartphone, as the Viamigo application to be used by the person with dementia is currently exclusively available for Android. Inclusion criteria informal caregivers: Family caregiver of participant diagnosed with mild to moderate dementia; Aged 18+; Having at least weekly contact with the person with dementia; Having an Android or Apple smartphone and laptop/computer. Exclusion Criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: No informed consent given; Concurrent participation in any other interventional study.

Sites / Locations

  • Maastricht UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Viamigo intervention

Arm Description

All eligible and consenting dyads will be asked to participate in the Viamigo intervention (mobile application), consisting of three main components: (1) a face-to-face technology training session of 60 minutes, (2) a 3-month period of using the Viamigo intervention with support phone calls of approximately 5 minutes by the coordinating investigator once every two weeks, and (3) an evaluation phone call of 5-10 minutes.

Outcomes

Primary Outcome Measures

Overall feasibility of Viamigo intervention
Semi-structured interviews with dyads (participants with dementia and informal caregivers)
Recruitment and drop-out rates
Number of referred dyads, number of eligible participants who are willing to participate, number of eligible participants who are not willing to participate, including reasons for declined participation (if provided); number of dropouts during the baseline assessment (after signing informed consent and before starting the intervention) as well as reasons for dropout, if provided; number of dropouts after starting the intervention and reasons for dropout, if provided
Recruitment time
Amount of spent time on recruiting participants (recruitment capability) in weeks
Data collection methods of Viamigo intervention
Notes on: if outcome measures were sensitive to change; how understandable data collection procedures were for study participants; and how much time was required to fill in questionnaires
Social validity of Viamigo intervention
measured by selfreported Program Participation Questionnaire (PPQ)
Practicality of Viamigo intervention
Practical constraints in the context and environment to implement the Viamigo intervention (e.g. time or resource availability) will be tracked with notes
Adaptability of Viamigo intervention
Aspects facilitating or impeding the flexibility of the intervention, as well as a potential needed set of requirements to implement the intervention with people with dementia and their informal caregivers will be tracked with notes

Secondary Outcome Measures

Change in out-of-home mobility of participants with dementia at 3 months
Measured by a travel diary
Change in social participation of participants with dementia at 3 months
Measured by the Engagement and Independence in Dementia Questionnaire (EID-Q), the Lubben Social Network Scale - 6 (LSNS-6), and the post-intervention semi-structured interview
Change in quality of life of informal caregivers at 3 months
Measured by the Investigating Choice Experiments CAPability measure for Older people (ICECAP-O)
Change in caregiver burden at 3 months
Measured by the Burden Scale for Family Caregivers - short version (BSFC-s)
Change in gains in dementia caregiving at 3 months
Measured by Gain in Alzheimer care INstrument (GAIN)

Full Information

First Posted
October 5, 2022
Last Updated
February 27, 2023
Sponsor
Maastricht University
search

1. Study Identification

Unique Protocol Identification Number
NCT05648864
Brief Title
Viamigo for People With Dementia and Their Informal Caregivers
Official Title
Geographic Information System (GIS) Based Intervention 'Viamigo' for People With Dementia and Their Informal Caregivers: A Single-arm Trial to Evaluate the Feasibility and Preliminary Participant Responses
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 7, 2023 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
August 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University

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
The main objective of this study is to evaluate the feasibility of the Geographic Information System (GIS)-based mobile application 'Viamigo' among people with dementia living in the community and their informal caregivers. Viamigo aims to support the independent out-of-home mobility of the user and to reduce informal caregiver's burden by teaching users a known individual route, which they can accomplish independently while being monitored by an informal caregiver. Although Viamigo was initially developed for persons with intellectual disabilities, it is expected that it can also support and improve out-of-home mobility and thereby the social participation of people with dementia. The design of the study is a mixed methods single-arm pre-post design with a baseline assessment, a 3-month intervention period, and a post-intervention assessment. Dyads (n=24) of people with mild to moderate dementia living in the community and their informal caregivers will use the mobile application for 3 months. The main study parameter is the feasibility of the Viamigo intervention for people with dementia and their informal caregivers. Secondary study parameters for people with dementia include out-of-home mobility and social participation. Secondary study parameters for informal caregivers include quality of life, caregiver burden, and gains in dementia caregiving.
Detailed Description
Rationale: People with dementia living in the community experience reduced out-of-home mobility and participate less in activities outside the home. This results in reduced social participation outside the home, which can negatively affect their health (e.g. leads to social isolation and increased risk of depressive symptoms). Technological interventions show promise in enhancing the social participation of people with dementia. However, there is a lack of technological interventions that facilitate social participation outside the home. While a growing body of evidence highlights the potential of Geographic Information Systems (GIS) in facilitating the out-of-home mobility of people with dementia and reducing informal caregivers' feelings of worry, very little attention is paid to the potential of GIS in enhancing the social participation of people with dementia. The GIS-based mobile application Viamigo aims to support the independent out-of-home mobility of the user and to reduce informal caregiver's burden by teaching users a known individual route, which they can accomplish independently afterwards while being monitored by an informal caregiver. Although Viamigo was initially developed for persons with intellectual disabilities, it is expected that it can also support and improve out-of-home mobility and thereby the social participation of people with dementia. Objective: The main objective of this study is to evaluate the feasibility of the Viamigo intervention among people with dementia living in the community and their informal caregivers. The secondary objective of this study is to assess the first responses of people with dementia and informal caregivers to the Viamigo intervention. Study design: This feasibility study includes a mixed methods single-arm pre-post design with a baseline assessment, a 3-month intervention period, and a post-intervention assessment. Study population: The study population consists of dyads (n=24) of people with mild to moderate dementia living in the community and their informal caregivers. There are no restrictions regarding sex, educational level, or cultural background. Intervention (if applicable): All eligible and consenting dyads will be asked to participate in the Viamigo intervention, consisting of three main components: (1) a face-to-face technology training session of 60 minutes, (2) a 3-month period of using the Viamigo intervention with support phone calls of approximately 5 minutes by the coordinating investigator once every two weeks, and (3) an evaluation phone call of 5-10 minutes. Main study parameters/endpoints: The main study parameter is the feasibility of the Viamigo intervention for people with dementia and their informal caregivers. Secondary study parameters for people with dementia include out-of-home mobility and social participation. Secondary study parameters for informal caregivers include quality of life, caregiver burden, and gains in dementia caregiving. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: People with dementia will be asked to fill in the same two questionnaires (approximately 20 minutes in total) during the baseline and post-intervention assessment. Additionally, they are asked to fill in a daily travel diary for one week at baseline and during the last week of the intervention period. Informal caregivers will be asked to fill in the same three questionnaires (approximately 25 minutes in total) during the baseline and post-intervention assessment, and another 15-minutes questionnaire during the post-intervention assessment. Additionally, a smaller sample of the dyads (10 dyads) will be asked to share their experiences using the Viamigo intervention in a semi-structured post-intervention interview of approximately 30 minutes. Dyads will be asked whether they prefer to conduct the different assessments at home or at another location (e.g. Maastricht University). By participating in the study, a participant with dementia might be more often exposed to potentially risky situations in his or her living environment (e.g. traffic). Participation in a technological intervention study can be time-consuming and demanding. One way to reduce the burden of the study is to give participants the freedom to use the Viamigo application at their own pace.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia
Keywords
social participation, community, technology, mobile application, feasibility

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
dyads of people living with dementia (n=24) and their informal caregivers (n=24)
Allocation
N/A
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Viamigo intervention
Arm Type
Experimental
Arm Description
All eligible and consenting dyads will be asked to participate in the Viamigo intervention (mobile application), consisting of three main components: (1) a face-to-face technology training session of 60 minutes, (2) a 3-month period of using the Viamigo intervention with support phone calls of approximately 5 minutes by the coordinating investigator once every two weeks, and (3) an evaluation phone call of 5-10 minutes.
Intervention Type
Device
Intervention Name(s)
Viamigo
Intervention Description
Mobile application with the aim to enhance the independent outdoor mobility of the user while a coach (informal caregiver) can monitor the route from a distance.
Primary Outcome Measure Information:
Title
Overall feasibility of Viamigo intervention
Description
Semi-structured interviews with dyads (participants with dementia and informal caregivers)
Time Frame
3 months
Title
Recruitment and drop-out rates
Description
Number of referred dyads, number of eligible participants who are willing to participate, number of eligible participants who are not willing to participate, including reasons for declined participation (if provided); number of dropouts during the baseline assessment (after signing informed consent and before starting the intervention) as well as reasons for dropout, if provided; number of dropouts after starting the intervention and reasons for dropout, if provided
Time Frame
3 months
Title
Recruitment time
Description
Amount of spent time on recruiting participants (recruitment capability) in weeks
Time Frame
3 months
Title
Data collection methods of Viamigo intervention
Description
Notes on: if outcome measures were sensitive to change; how understandable data collection procedures were for study participants; and how much time was required to fill in questionnaires
Time Frame
3 months
Title
Social validity of Viamigo intervention
Description
measured by selfreported Program Participation Questionnaire (PPQ)
Time Frame
3 months
Title
Practicality of Viamigo intervention
Description
Practical constraints in the context and environment to implement the Viamigo intervention (e.g. time or resource availability) will be tracked with notes
Time Frame
3 months
Title
Adaptability of Viamigo intervention
Description
Aspects facilitating or impeding the flexibility of the intervention, as well as a potential needed set of requirements to implement the intervention with people with dementia and their informal caregivers will be tracked with notes
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change in out-of-home mobility of participants with dementia at 3 months
Description
Measured by a travel diary
Time Frame
3 months
Title
Change in social participation of participants with dementia at 3 months
Description
Measured by the Engagement and Independence in Dementia Questionnaire (EID-Q), the Lubben Social Network Scale - 6 (LSNS-6), and the post-intervention semi-structured interview
Time Frame
3 months
Title
Change in quality of life of informal caregivers at 3 months
Description
Measured by the Investigating Choice Experiments CAPability measure for Older people (ICECAP-O)
Time Frame
3 months
Title
Change in caregiver burden at 3 months
Description
Measured by the Burden Scale for Family Caregivers - short version (BSFC-s)
Time Frame
3 months
Title
Change in gains in dementia caregiving at 3 months
Description
Measured by Gain in Alzheimer care INstrument (GAIN)
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Stage of dementia
Description
Measured by the Clinical Dementia Rating (CDR)
Time Frame
week 0 (baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria people with dementia: Capacity to give informed consent; Diagnosis of mild to moderate dementia as evaluated by a healthcare professional and as reported by the person with dementia and the informal caregiver (by asking when and where the person has been diagnosed and by who); Living in the community (alone or with family/roommate(s)/friends); Taking part in social activities outside the home; Availability of an informal caregiver who is interested to take part in this study; Having an Android smartphone, as the Viamigo application to be used by the person with dementia is currently exclusively available for Android. Inclusion criteria informal caregivers: Family caregiver of participant diagnosed with mild to moderate dementia; Aged 18+; Having at least weekly contact with the person with dementia; Having an Android or Apple smartphone and laptop/computer. Exclusion Criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: No informed consent given; Concurrent participation in any other interventional study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pascale Heins, MSc
Phone
0031433881022
Email
p.heins@maastrichtuniversity.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marjolein E. de Vugt, Prof.
Organizational Affiliation
Maastricht University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maastricht University
City
Maastricht
ZIP/Postal Code
6229 ET
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pascale Heins, MSc
Phone
0031433881022
Email
p.heins@maastrichtuniversity.nl
First Name & Middle Initial & Last Name & Degree
Marjolein E de Vugt, Prof
First Name & Middle Initial & Last Name & Degree
Frans RJ Verhey, Prof
First Name & Middle Initial & Last Name & Degree
Lizzy MM Boots, PhD
First Name & Middle Initial & Last Name & Degree
An Neven, PhD
First Name & Middle Initial & Last Name & Degree
Pascale Heins, MSc

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After completion of the study, an anonymised version of the data will be made available for reuse on a data repository, such as Dataverse.nl. No personal data will be included. Access to this data will be allowed under specified conditions (still in discussion with the legal advisor of Maastricht University). All participants will be asked for consent to reuse their data.
IPD Sharing Time Frame
Anonymised data will become available right after the completion of the study. All data will be securely stored and available for 15 years after the last publication on the data.
IPD Sharing Access Criteria
Access to the data collection will be restricted by conditions for use. These conditions will be determined in consultation with a legal adviser of Maastricht University. The legal adviser has been contacted via e-mail (privacy@maastrichtuniversity.nl).

Learn more about this trial

Viamigo for People With Dementia and Their Informal Caregivers

We'll reach out to this number within 24 hrs