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Clinical study on total hip arthroplasty patients with instrumented shoes

Clinical study on total hip arthroplasty patients with instrumented shoes - Using instrumented shoes in THA patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37965
Enrollment
25
Registered
2011-06-10
Start date
2011-07-08
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Osteoarthritis in the hip/Wear and tear of hipjoint

Interventions

None listed

Sponsors

Universiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: •Age between 50 and 80 years. •Primary, unilateral, osteoarthritis of the hip. •Patients should be selected for a primary THA and undergo the operation within the next 4 months.

Exclusion criteria

Exclusion criteria: •Have bilateral THA. •Have any kind of leg arthroplasties. •Have rheumatoid arthritis •Have any neurological disorder. •Not able to perform the tasks because of pain or impairment. •Suffering also from other degenerative diseases. •Develop a bilateral disease. •Revision/re-operations of primary hip prosthesis •Unable to understand instructions or the questionnaire

Design outcomes

Primary

MeasureTime frame
The main study parameter will be the gait velocity calculated through the IFS (product of the stride length and the stride frequency).

Secondary

MeasureTime frame
Stride length and stride frequency separately as well as the symmetry in ground reaction force will be the secondary parameters. In addition, the IFS parameters correlated to the gait velocity (assessed independently from the IFS) and the outcome of the questionnaires (HHS, WOMAC-FC and VAS) are secondary parameters.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)