Detectie van loopperioden, beweegintensiteit en specifieke aan claudicatio intermittens gerelateerde loopstops met de Dynaport MoveMonitor.

Detection of walking periods and intermittent claudication specific walking stops using the Dynaport MoveMonitor. A validation study.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON24139

Enrollment

Registered

2011-06-29

Start date

2011-07-01

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

intermittent claudication

Interventions

Dynport MoveMonitor measuring device.

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with intermittent claudication determined with an EAI of <0.9 of <0.15 decrease after exercise; 2. Initial maximal walking distance <500m; 3. Age + gender matched control group of healty volunteers.

Exclusion criteria

Exclusion criteria: Comorbidity which could influence the walking distance, for instance: 1. COPD Gold 3-4; 2. Heart failure (NYAH 2 or more); 3. Severe artrosis; 4. Amputation; 5. Walking aids. For the control group there should be no history of peripheral arterial disease besides the above mentioned criteria.

Design outcomes

Primary

Measure	Time frame
1. Number of walking stops caused by intermittent claudication; 2. Painfree walking distance; 3. Functional walking distance.	—

Secondary

Measure	Time frame
1. Walking distance; 2. Walking speed; 3. Walking time; 4. Pain-scores (VAS).	—

Contacts

Public ContactGert-Jan Lauret

Catharina ziekenhuis Eindhoven Polikliniek Heelkunde Postbus 1350

movepad@gmail.com+31 (0)40 2398764

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)