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Adherence monitoring of use of custom-made orthopaedic shoes

Adherence monitoring of use of custom-made orthopaedic shoes - Use of custom-made orthopaedic shoes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43244
Enrollment
1000
Registered
2017-01-06
Start date
2017-01-03
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

Diabetes neurologic disorders

Interventions

Intervention: 300 participants are included in the intervention study: 100 in the control group without knowledge about the actual purpose of the study (adherence monitoring based on temperature dat
Adherence
orthopaedic shoes

Sponsors

Revalidatie
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * Patients with a prescription for their first pair of OS * Mentally competent (*wilsbekwaam*) * Aged 18 years and older. * Able to read and speak Dutch

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Main study parameters: Objective (Orthotimer sensor) and subjective (diary and MOS) use of OS (in days/week and hours/days), relative use of OS (actual use of OS as a percentage of intended use of OS), number of OS adjustments, use and usability of OS measured with a validated questionnaire (MOS).

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)