Feasibility of Home-based Measurement of Walking Capacity Using Global Positioning System in Peripheral Artery Disease (POST-GPS)

University Hospital, Angers

Status: Completed

Conditions: Peripheral Artery Disease

Treatments: Procedure: GPS recording(s) of walking capacity in PAD patients

Study type: Observational

Funder types: Other

Identifiers

NCT01141361

POST-GPS

Details and patient eligibility

About

The purpose of this study is to assess the feasibility of home-based measurement of walking capacity in peripheral arterial disease (PAD) patients, uing the Global Positioning System (GPS). This study should state if the GPS technique could be used in clinical routine in order to assess walking capacity in PAD patients. Patients will be assessed a first time (test 1) and six months later (test 2).

Full description

The measurement of walking capacity in PAD patients is an important step in the management of such patients. The gold standard method to assess this walking capacity is the measurement of the maximal walking distance on a treadmill. However, treadmill measurement are not readily accessible and the relationship with free-living walking capacity is, although not well known, weak. A novel approach was developed using a Global Positioning System in order to assess community-based walking capacity. This method showed interesting results, validating the technique, but was limited to one laboratory and to the place where the measurements were performed. The next step is therefore to assess the feasibility of home-based measurement of walking capacity using the GPS technique, through a multicenter study regrouping university hospitals, independent vascular specialists (angiologists) and private clinic(s).

Enrollment: 251 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• ABI < 0.90 or patients with vascular history (surgery, endovascular treatment) and having vascular type claudication
• Older than 18 years
• Vascular-type claudication (defined by the Leriche classification and the Edimbourg questionnaire criterion)
• Informed consent of the patient

Non-Inclusion Criteria:

• No informed consent of the patient
• Exercise (walking) limitation other than vascular explained limitation
• Critical limb ischemia (Leriche stage 3 or 4)
• Major cardiovascular events in the last 3 months
• Pregnant woman
• Patient unable to understand the protocol of the study

Exclusion criteria

• Withdrawal of the informed consent of the patient following the inclusion period
• Emergence of a non-inclusion criteria during the inclusion period
• Patient with a GPS maximal walking distance > 2000 meters following the first evaluation (can not be considered as having a major walking limitation)

Trial design

251 participants in 1 patient group

Peripheral arterial disease patients

Description:

Patients with a peripheral arterial disease, defined by an ankle to brachial index below 0.90

Treatment:

Procedure: GPS recording(s) of walking capacity in PAD patients