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SensiStep Study Resumption of weight bearing among total hip prosthesis patients; a pilot study

SensiStep Study Resumption of weight bearing among total hip prosthesis patients; a pilot study - SensiStep Study in Total Hips

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON41048
Enrollment
24
Registered
2015-01-07
Start date
2015-05-10
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

arthrosis of the hip joint coxarthrosis

Interventions

Weight bearing is registered in both study groups with the SensiStep system. In the intervention group, direct feedback will be given during the weight bearing using a wrist device. Using this devic

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age between 60 and 85 years Elective surgical total hip prosthesis for coxarthrosis Postoperative full weight bearing

Exclusion criteria

Exclusion criteria: Lack of informed consent Cognitive impairment, either pre-existent or occuring in the first day or days after surgery Insufficient knowledge of Dutch language Pre-opeartive comorbidity influencing the mobility other than coxarthrosis (e.g. confined to wheelchair, walking distance

Design outcomes

Primary

MeasureTime frame
The primary outcome parameters are generated by the SensiStep system: - Loading rate - The number of steps per time unit - The number of Periods of Dynamic Loading, PDL

Secondary

MeasureTime frame
N.A.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)