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Clinical Trials/NCT02878954
NCT02878954
Unknown
Not Applicable

Exercise in Peripheral Artery Disease - Gender-specific Differences and Unexplored Opportunities in Women: the GrEnADa-project

KU Leuven0 sites160 target enrollmentJanuary 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Peripheral Artery Disease
Sponsor
KU Leuven
Enrollment
160
Primary Endpoint
Barriers towards exercise assessed by questionnaires in patients with peripheral artery disease.
Last Updated
9 years ago

Overview

Brief Summary

This research project aims to investigate the gender-based difference in patients with peripheral artery disease. To attend this, this study has two specific objectives:

Objective 1: To identify gender-specific barriers towards exercise and physical activity in patients with peripheral artery disease (PAD).

Objective 2: To evaluate gender-specific differences in functional capacity and cardiovascular function and regulation in patients with PAD at rest, during and following a single session of maximal exercise.

Registry
clinicaltrials.gov
Start Date
January 2017
End Date
December 2019
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
KU Leuven
Responsible Party
Principal Investigator
Principal Investigator

Véronique Cornelissen

PhD

KU Leuven

Eligibility Criteria

Inclusion Criteria

  • Ankle-brachial index (ABI) ≤ 0.9 in one or two legs
  • Fontaine stage II of PAD
  • Body mass index \<35 kg/m2
  • Resting systolic blood pressure (BP) \<160 mmHg and diastolic BP \<105 mmHg
  • Ability to walk at least 2min at 3.2 km/h
  • Ability to undertake an incremental treadmill test
  • Decrease of at least 15% in ABI after a maximal treadmill test
  • Not currently engaging in any regular exercise program

Exclusion Criteria

  • Exercise induced signs of myocardial ischemia or complex ventricular arrhythmias
  • Cardiovascular autonomic neuropathy
  • Use of beta-blocker
  • Nondihydropyridine calcium antagonists or insulin and hormone replacement therapy

Outcomes

Primary Outcomes

Barriers towards exercise assessed by questionnaires in patients with peripheral artery disease.

Time Frame: Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.

After completion of the 6-minute walking test, patients will be asked to fill in the following questionnaires: walking impairment questionnaire, walking estimated-limitation calculated by history (WELCH), San Diego Claudication Questionnaire, SF-36 and two questionnaires for personal and environmental barriers to physical activity.

Gender-specific differences in walk capacity in patients with peripheral artery disease

Time Frame: Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.

The measurements of this outcome will be performed in a second visit day, separated by at least 48h from visit 1 (outcome 1). Patients will perform a maximal exercise test to determine claudication onset distance (m) defined as the distance walked until the patients first reported pain in the leg during the treadmill test and total walk distance (m) defined as the total distance that the patient was able to walk during the test.

Gender-specific differences in functional capacity in patients with peripheral artery disease

Time Frame: Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.

Walking economy defined as VO2 measured during the first stage of the treadmill test and functional capacity defined as VO2 peak obtained during the test will be obtained.

Secondary Outcomes

  • Gender-specific differences in vascular function in patients with peripheral artery disease at rest and after a maximal exercise test(Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.)
  • Gender-specific differences in autonomic modulation at rest and after a maximal exercise test(Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.)
  • Gender-specific differences in physical activity level measured by accelerometer(Cross-sectional study. This outcome will be measured through study completion, an average of 18 months.)

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