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Evaluation of a mobile application for independent cognitive training – effects on cognitive abilities and quality of life in patients with Parkinson’s disease (PD) and mild cognitive impairment (MCI)

Evaluation of a mobile application for independent cognitive training – effects on cognitive abilities and quality of life in patients with Parkinson’s disease (PD) and mild cognitive impairment (MCI) - IPS-NeNaE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00040251
Enrollment
50
Registered
2026-05-21
Start date
2023-01-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

G20 F06.7

Interventions

Group 1: Participants with idiopathic Parkinson’s disease and mild cognitive impairment receive app-based cognitive training using NeuroNation MED for 12 weeks. Training is performed three times per w

Sponsors

Asklepios Fachklinikum
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of idiopathic Parkinson’s disease (ICD-10: G20) Mild cognitive impairment (MCI/F06.7) Mild impairment in at least one CERAD subdomain Capacity to provide informed consent Ability to use a mobile device Availability of a mobile device Ability to understand German-language instructions

Exclusion criteria

Exclusion criteria: Moderate or severe dementia Severe cognitive impairment (CERAD z < -1.64) Legal guardianship Paresis of the dominant hand or arm Relevant visual field deficits Severe non-correctable visual impairment Severe aphasia Use of other cognitive training programs or training applications

Design outcomes

Primary

MeasureTime frame
Change in general cognitive performance after 12 weeks of intervention measured by the Neuropsychological Assessment Battery (NAB). Time points: Baseline (T1); After 12 weeks (T2) Assessment method: Standardized neuropsychological assessment using the NAB.

Secondary

MeasureTime frame
Changes in psychological well-being, self-efficacy, depressive symptoms, subjective cognitive functioning, health-related quality of life, health literacy, and usability after 12 weeks. Assessment instruments: Health-49 HADS-D FLei PDQ-39 HLQ-G System Usability Scale (SUS) Time points: Baseline (T1); After 12 weeks (T2)

Countries

Germany

Contacts

Public ContactDavid Weise

Asklepios Fachklinkikum

da.weise@asklepios.com+4936428561375

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026