Monitor-Mi Study Digital Self-Monitoring in People with Mild Cognitive Impairment

Monitor-Mi Study: Digital Self-Monitoring in People with Mild Cognitive Impairment. An evaluation of the feasibility and validity of the PsyMate application in people with mild cognitive impairment

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON24090

Enrollment

Registered

2017-12-11

Start date

2018-03-01

Completion date

Unknown

Last updated

2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Before entering the study, participants will be screened to make sure that they meet all of the inclusion criteria. After informed consent is obtained, the study protocol for each participant includes

Eligibility

Inclusion criteria

Inclusion criteria: - Having a clinical diagnosis of MCI, according to Petersen (2004) criteria - In possession of a smartphone with an operation system from android or iOS. - Written informed consent is obtained from the person with MCI as well as the relevant other.

Exclusion criteria

Exclusion criteria: - Subjects with MCI who have insufficient cognitive abilities to engage with the PsyMate application (based on clinical judgment). - Subjects with MCI who have severe health problems (based on clinical judgment) such as a diagnosis of somatic, psychiatric or neurological disorder potentially causing cognitive dysfunction.

Design outcomes

Primary

Measure	Time frame
The primary objective of this study is to evaluate the feasibility and validity of the ESM use implemented in the PsyMate application in people with MCI.	—

Secondary

Measure	Time frame
No secondary outcome	—

Contacts

Public ContactSara Laureen Bartels

kamer 4.G3.067

sara.bartels@maastrichtuniversity.nl043 38 81321

Outcome results