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Use of auditory feedback to improve a patients compliance with partial weight bearing

Use of an Auditory BioFeedback system to improve a patient's Partial Weight Bearing compliance: A feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29061
Enrollment
20
Registered
2015-04-09
Start date
2015-05-01
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

Anterior cruciate ligament reconstruction

Interventions

In this study an auditory biofeedback (ABF) device, giving feedback about partial weight bearing (PWB) to the paient will be tested. The device consists out of a measurement insole embedded in a sanda

Sponsors

University Medical Center Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Patients recovering from ACL reconstruction - Younger than 65 years of age - Able to walk with crutches - Able to speak Dutch

Exclusion criteria

Exclusion criteria: - Significant orthopeadic disturbances or pain - serious co-morbidities - Clinically significant hearing problems - Clinically significant neurological problems

Design outcomes

Primary

MeasureTime frame
1. Percentage of incorrect steps: This parameter will be used to evaluate the difference in fractions of incorrect steps, with or without the use of the ABF device. 2. Time interval between incorrect steps (exeeding either the maximum or minimum allowed weight): This parameter will be used to indicate the learning curve involved in adapting to the use of an ABF device.

Secondary

MeasureTime frame
An interview will be conducted after the seccond session, giving an indication of user acceptance of the auditory biofeedback training in general and the tested ABF device.

Contacts

Public ContactIris Bokkes

University Medical Center Groningen, University of Groningen

i.bokkes@student.rug.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)