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Structured Home-based Exercise Versus Walking Advice in Claudication Patients: a Randomized-controlled Trial

Primary Purpose

Peripheral Artery Disease

Status
Active
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Structured home-based exercise
Walking advice
Sponsored by
University Hospital of Ferrara
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Artery Disease focused on measuring exercise, rehabilitation, exercise testing

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • male and females aged > 60 years old
  • peripheral artery disease at Leriche-Fontaine's stage 2a or 2b
  • cognitive functioning to give informed consent identified by a Mini Mental Status Examination score ≥18/30.

Exclusion Criteria:

  • peripheral artery disease at Leriche-Fontaine's stage 1
  • peripheral artery disease at Leriche-Fontaine's stage 3 or more
  • severe cardio-respiratory conditions (e.g. unstable angina; severe heart failure identified by New York Heart Association class III or IV)
  • neurological or musculoskeletal conditions (e.g. above knee amputation) contraindicating or inhibiting exercise training.
  • very good exercise capacity determined by a 6-minute walking distance > 500 meters.

Sites / Locations

  • University Hospital of Ferrara

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Structured home-based exercise

Walking advice

Arm Description

Program will include two 10-minute sessions/day (6 days/week) of intermittent walking (1-minute work and 1-minute rest while seated) at a prescribed speed converted into a walking cadence and followed at home using a metronome. The walking sessions will be preferably performed indoors at home or on a treadmill. During the study, 2 follow-up visits (at weeks 8 and 16) will be performed to evaluate patient adherence to the program and to update the exercise program with the duration of each session that remained constant. The walking intensity of each exercise regime will be progressively modified to increase the training load. The patients will be asked to fill out a daily training record indicating completion of the exercise and any associated symptoms. Patients will have the ability to contact the rehabilitation team, composed of a physician and a sports science expert, throughout the entire study period via phone.

Patients will receive advice to walk as suggested by the guidelines. In particular, a team member will recommend patients to gather almost 30 minutes of walking at least 3 times per week; when the patient will face claudication pain, he/she will be allowed to rest, and restart walking as soon as possible. A daily log to be compiled will be provided to each patients to record the amount of walk performed.

Outcomes

Primary Outcome Measures

6-Minute Walking Test (mobility)
Subjects will be instructed to walk as far as possible on a 21m walkway in 6 minutes, with their habitual walking device, with the possibility to slow down and rest if necessary. The total distance walked, the pain-free walking distance, and the perceived exertion at the end of the test will be recorded.

Secondary Outcome Measures

Ankle Brachial Index (hemodynamics)
The ankle-brachial index (ABI) is the ratio of the blood pressure at the ankle to the blood pressure in the upper arm (brachium). The ABI is calculated by dividing the systolic blood pressure measured at the ankle for both limbs with the patient in supine position by the systolic blood pressure in the arm.
Vascu-QoL-6 (health-related quality of life)
This questionnaire consists of 6 items with a score ranging from 1 to 4 examining various aspects of disease-related quality of life. Higher scores correspond to better quality of life.
5-time sit-to-stand test (lower limbs strength)
This test consists in moving from a sitting position to a standing position on a 42- cm high chair as quick as possible, for five times, with arms folded across the chest. Time will be taken when the test starts, and when the patient lay his/her buttocks on the chair for the fifth time.
Foot temperature
Foot temperature will be noninvasively measured through an infrared thermal imaging camera at the dorsum of each foot at three points
Number and rate of hospitalizations
Number and rate of all-cause hospitalizations within participants will be collected.
Number and rate of mortality
Number and rate of all-cause mortality within participants will be collected.

Full Information

First Posted
February 9, 2021
Last Updated
November 2, 2022
Sponsor
University Hospital of Ferrara
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1. Study Identification

Unique Protocol Identification Number
NCT04751890
Brief Title
Structured Home-based Exercise Versus Walking Advice in Claudication Patients: a Randomized-controlled Trial
Official Title
Effectiveness of a Home-based Structured Exercise Program Versus Walking Advice in Patients With Peripheral Artery Disease: a Randomized-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital of Ferrara

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A recent position paper calls for effective home-based exercise program for patients with peripheral artery disease (PAD) and claudication to be implemented in real-world care. This randomized-controlled trial aims to test the effects on mobility, hemodynamics and cardiovascular outcomes of a structured home-based exercise program (SHB) compared to walking advice (WA) recommendation intended as usual care, in PAD patients. Male and females PAD patients at Leriche-Fontaine's stage II and aged more than 60 years old will be enrolled. Patients will be randomized in SHB or WA groups. Patients of SHB group will receive a prescription of a home-based walking program during serial testing sessions at the hospital. The program will include two 10-minute sessions/day (6 days/week) of intermittent walking (1-minute work and 1-minute rest while seated) at a prescribed speed converted into a walking cadence and followed at home using a metronome. Two follow-up visits (at weeks 8 and 16) will be performed to evaluate patient adherence and to update the exercise program by increasing the walking speed. Patients randomized in WA group will receive the advice to walk as suggested by the guidelines. In particular, patients will be recommended to gather almost 30 minutes of walking at least 3 times per week; when they will face claudication pain, they will be allowed to rest and restart walking as soon as possible. Outcome measures will be performed at the entry prior to randomization, at the end of exercise programs (6-month) and after 12-month follow up. Primary outcomes will be the pain-free walking distance and the 6-minute walking distance collected during the 6-minute walking test Secondary outcomes will include ankle-brachial index, quality of life, lower limb strength and long-term clinical outcomes including revascularization and mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Artery Disease
Keywords
exercise, rehabilitation, exercise testing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Outcome assessors will be blinded to patients' allocation
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Structured home-based exercise
Arm Type
Experimental
Arm Description
Program will include two 10-minute sessions/day (6 days/week) of intermittent walking (1-minute work and 1-minute rest while seated) at a prescribed speed converted into a walking cadence and followed at home using a metronome. The walking sessions will be preferably performed indoors at home or on a treadmill. During the study, 2 follow-up visits (at weeks 8 and 16) will be performed to evaluate patient adherence to the program and to update the exercise program with the duration of each session that remained constant. The walking intensity of each exercise regime will be progressively modified to increase the training load. The patients will be asked to fill out a daily training record indicating completion of the exercise and any associated symptoms. Patients will have the ability to contact the rehabilitation team, composed of a physician and a sports science expert, throughout the entire study period via phone.
Arm Title
Walking advice
Arm Type
Active Comparator
Arm Description
Patients will receive advice to walk as suggested by the guidelines. In particular, a team member will recommend patients to gather almost 30 minutes of walking at least 3 times per week; when the patient will face claudication pain, he/she will be allowed to rest, and restart walking as soon as possible. A daily log to be compiled will be provided to each patients to record the amount of walk performed.
Intervention Type
Behavioral
Intervention Name(s)
Structured home-based exercise
Intervention Description
Low-intensity interval walking program prescribed at hospital and performed at daily at home
Intervention Type
Behavioral
Intervention Name(s)
Walking advice
Intervention Description
Walking advice according to the guidelines for peripheral artery disease patients
Primary Outcome Measure Information:
Title
6-Minute Walking Test (mobility)
Description
Subjects will be instructed to walk as far as possible on a 21m walkway in 6 minutes, with their habitual walking device, with the possibility to slow down and rest if necessary. The total distance walked, the pain-free walking distance, and the perceived exertion at the end of the test will be recorded.
Time Frame
Change at 6-month (end of training) respect to baseline
Secondary Outcome Measure Information:
Title
Ankle Brachial Index (hemodynamics)
Description
The ankle-brachial index (ABI) is the ratio of the blood pressure at the ankle to the blood pressure in the upper arm (brachium). The ABI is calculated by dividing the systolic blood pressure measured at the ankle for both limbs with the patient in supine position by the systolic blood pressure in the arm.
Time Frame
Change at 6-month (end of training) respect to baseline
Title
Vascu-QoL-6 (health-related quality of life)
Description
This questionnaire consists of 6 items with a score ranging from 1 to 4 examining various aspects of disease-related quality of life. Higher scores correspond to better quality of life.
Time Frame
Change at 6-month (end of training) respect to baseline
Title
5-time sit-to-stand test (lower limbs strength)
Description
This test consists in moving from a sitting position to a standing position on a 42- cm high chair as quick as possible, for five times, with arms folded across the chest. Time will be taken when the test starts, and when the patient lay his/her buttocks on the chair for the fifth time.
Time Frame
Change at 6-month (end of training) respect to baseline
Title
Foot temperature
Description
Foot temperature will be noninvasively measured through an infrared thermal imaging camera at the dorsum of each foot at three points
Time Frame
Change at 6-month (end of training) respect to baseline
Title
Number and rate of hospitalizations
Description
Number and rate of all-cause hospitalizations within participants will be collected.
Time Frame
6-month, 12-month and 24-month (follow up)
Title
Number and rate of mortality
Description
Number and rate of all-cause mortality within participants will be collected.
Time Frame
6-month, 12-month and 24-month (follow up)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male and females aged > 60 years old peripheral artery disease at Leriche-Fontaine's stage 2a or 2b cognitive functioning to give informed consent identified by a Mini Mental Status Examination score ≥18/30. Exclusion Criteria: peripheral artery disease at Leriche-Fontaine's stage 1 peripheral artery disease at Leriche-Fontaine's stage 3 or more severe cardio-respiratory conditions (e.g. unstable angina; severe heart failure identified by New York Heart Association class III or IV) neurological or musculoskeletal conditions (e.g. above knee amputation) contraindicating or inhibiting exercise training. very good exercise capacity determined by a 6-minute walking distance > 500 meters.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabio Manfredini, MD, PhD
Organizational Affiliation
University of Ferrara and University Hospital of Ferrara
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Ferrara
City
Ferrara
ZIP/Postal Code
44124
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results published at the end of the trial after deidentification.
IPD Sharing Time Frame
Individual participant data will be available beginning 6 months following study results publication.
IPD Sharing Access Criteria
Anyone who wishes to access the data.
Citations:
PubMed Identifier
18503221
Citation
Manfredini F, Malagoni AM, Mascoli F, Mandini S, Taddia MC, Basaglia N, Manfredini R, Conconi F, Zamboni P. Training rather than walking: the test in -train out program for home-based rehabilitation in peripheral arteriopathy. Circ J. 2008 Jun;72(6):946-52. doi: 10.1253/circj.72.946.
Results Reference
background
PubMed Identifier
30586765
Citation
Treat-Jacobson D, McDermott MM, Bronas UG, Campia U, Collins TC, Criqui MH, Gardner AW, Hiatt WR, Regensteiner JG, Rich K; American Heart Association Council on Peripheral Vascular Disease; Council on Quality of Care and Outcomes Research; and Council on Cardiovascular and Stroke Nursing. Optimal Exercise Programs for Patients With Peripheral Artery Disease: A Scientific Statement From the American Heart Association. Circulation. 2019 Jan 22;139(4):e10-e33. doi: 10.1161/CIR.0000000000000623. No abstract available.
Results Reference
background
PubMed Identifier
34068534
Citation
Manfredini F, Lamberti N, Traina L, Zenunaj G, Medini C, Piva G, Straudi S, Manfredini R, Gasbarro V. Effectiveness of Home-Based Pain-Free Exercise versus Walking Advice in Patients with Peripheral Artery Disease: A Randomized Controlled Trial. Methods Protoc. 2021 May 10;4(2):29. doi: 10.3390/mps4020029.
Results Reference
derived

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Structured Home-based Exercise Versus Walking Advice in Claudication Patients: a Randomized-controlled Trial

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