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WalkWell Gait reTrainer: Remote patient monitoring and gait retraining for knee OA

WalkWell Gait reTrainer: Remote patient monitoring and gait retraining for knee OA - WalkWell Gait reTrainer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57285
Enrollment
30
Registered
2024-07-30
Start date
2025-04-07
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

degenerative joint disease osteoarthritis joint disorder

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy controls: over 45 years old able to walk for at least 15 to 30 minutes for 3 to 7 days per week without any walking aids Physiotherapists: work for at least two years as a physiotherapist in primary care provide treatment for patients with knee complaints two or more times per week have affinity with technical developments in physiotherapy care

Exclusion criteria

Exclusion criteria: Healthy controls: Activity-related knee pain and morning knee stiffness or stiffness of 30 minutes or more. Traumatic knee injury or surgery in the past year. Any neurological, rheumatological, or metabolic disorders affecting mobility. Other diagnosed causes of knee symptoms (e.g. tendonopathy). Musculoskeletal conditions affecting the ankles, hips, pelvis or lumbar spine. Body mass index > 35 kg/m2. Cognitive impairments. Unable to communicate in either Dutch or English

Design outcomes

Primary

MeasureTime frame
Qualitative data from participants and physiotherapists on how they use the WalkWell Gait reTrainer (i.e. user experience). We will also explore the participant*s ability to consistently alter their FPA in response to the feedback given by the WallWell Gait reTrainer, and their ability to maintain their target FPA over a short period of one week (i.e. feasibility).

Secondary

MeasureTime frame
Quantify correlations among the data collected and evaluate the associations between biomechanical parameters and other variables including participant demographics.

Countries

Netherlands

Contacts

Public ContactEM Macri

Erasmus MC, Universitair Medisch Centrum Rotterdam

walkwell@erasmusmc.nl010-7034686

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)