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Translation and validation of the Dutch System Usability Scale

Translation and validation of the System Usability Scale – Dutch version

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27796
Enrollment
60
Registered
2021-01-05
Start date
2021-01-10
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Not relevant

Interventions

None listed

Sponsors

Sint Maartenskliniek
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Adult patient or therapist (18 years or older). - Able to understand the Dutch language. - Experience (for at least 4 different moments in time) with either walking assistance devices (ankle-foot orthosis, Rewalk), eHealth applications (Dr. Bart App) or training devices (GRAIL, C-Mill, Zero-G, Lokomat).

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
The main study parameter is the construct validity of the D-SUS according to the definition of the COSMIN Criteria. Correlations between D-SUS, D-QUEST, and the general usability question (‘Overall, how would you rate the application on a scale from 0 to 10?’) will be assessed by the Spearman Correlation Coefficient (level of significance p0.8) as a measure of construct validity.

Secondary

MeasureTime frame
The secondary study parameter is test-retest reliability of the D-SUS. This will be determined by Blant-Altman plots, Intraclass Correlation Coefficient (ICC) and percentage of agreement between the results of the first and second moment of filling out the D-SUS, D-QUEST, and the general usability question.

Contacts

Public ContactCarmen Ensink

Sint Maartenskliniek

c.ensink@maartenskliniek.nl024-365 9140

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)