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Digital Support for Supervised Exercise Therapy in Peripheral Arterial Disease (TrackPAD)

Primary Purpose

Peripheral Arterial Disease

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
trackPAD
Sponsored by
University Hospital, Essen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Arterial Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of lower extremity PAD based on (and/or):

    • ABI ≤ 0.9 in at least one legs
    • Invasive or non-invasive imaging of stenotic lower extremity artery disease
    • Endovascular or surgical revascularization of lower extremity artery
  • PAD Fontaine Stage IIa/b
  • Smartphone with possibility to use TrackPAD: Android ≥ 5.0 or IOS ≥ 11.0
  • Written informed consent prior to any study procedures, including a specified follow-up evaluation
  • Best-medical treatment in the last 2 months in accordance with standard guidelines

Exclusion Criteria:

  • Wheelchair bound, use of walking aid or walking impairment due to another cause than PAD
  • Below or above knee amputation
  • Acute or critical limb ischemia
  • PAD Fontaine Stage I or III / IV
  • No German knowledge
  • Severe cognitive dysfunction
  • Congestive heart failure with NYHA III-IV symptoms
  • Active congestive heart failure requiring the initiation or uptitration of diuretic therapy
  • Angina pectoris with CCS class 3-4 symptoms or myocardial infarction or stroke in the last 3 months
  • Active arrhythmia requiring the initiation or uptitration of anti-arrhythmic therapy
  • Severe valve disease

Sites / Locations

  • Department of Cardiology and Vascular Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

intervention group

control group

Arm Description

in addition to the usual therapy, the patients were given access to the trackPAD app

patients in this group were treated as usual in the clinic without additional interventions.

Outcomes

Primary Outcome Measures

change in 6-minutes walking distance
measured via GPS with the trackPAD app

Secondary Outcome Measures

change in physical activity, measured in patients' self-report on how many days a week on average they engage in a physical activity that causes them to sweat or get out of breath, and how many minutes on average they spend doing it.
to compare the two groups groups in terms of physical endurance, the self-reported physical activity was recorded
peripheral arterial disease-related quality of life
measured with the Peripheral artery disease Quality of Life Questionnaire (PADQOL) questionnaire, a validated PAD-specific questionnaire. Minimum score is 38 and maximum is 228, with higher values indicating a better outcome.
Usability of the TrackPAD app
measured with the User version of the Mobile Application Rating Scale (uMars) questionnaire. The uMARS includes 3 factors, namely app quality, app subjective quality and perceived impact. Minimum score of the app quality scale is 4 and the maximum is 20. The App Subjective Quality scale has a minimum of 4 and a maximum of 20, and the Perceived Impact scale has a minimum of 6 and a maximum of 30. Higher values indicate a better outcome.

Full Information

First Posted
June 9, 2021
Last Updated
June 23, 2021
Sponsor
University Hospital, Essen
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1. Study Identification

Unique Protocol Identification Number
NCT04947228
Brief Title
Digital Support for Supervised Exercise Therapy in Peripheral Arterial Disease
Acronym
TrackPAD
Official Title
Supervised Exercise Therapy Using Mobile Health Technology in Patients With Peripheral Arterial Disease: Randomized Controlled Pilot Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
December 6, 2018 (Actual)
Primary Completion Date
March 28, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Essen

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
The individual restrictions of daily life for patients with PAD are more important than statistical facts for mortality and morbidity. Intermittent claudication causes a progressive reduction of the pain-free walking distance (PWD) as an expression of a worsening PAD. This decrease in physical capability results in a decline of mental health and relevantly reduces the patients' quality of life (QoL). Supervised exercise therapy (SET) is a cornerstone in the conservative management of intermittent claudication and extends the PWD. Even though SET is easy to practice and highly cost effective, the adherence to perform SET on a regular base is rather low. The underuse of exercise can be partly explained by the lack of institutional resources, but also by both patients' and physicians' lack of interest in exercise. Mobile health (mHealth) technologies increase the incentives and provide digital support for patients with PAD on several treatment levels. They might lead to a higher adherence to exercise training and offer new scopes in patient-centered healthcare, but so far studies show opposite results. Because app stores are flooded with health and fitness apps, specific support tools are highly desired by patients with PAD and PAD-specific solutions are missing so far. Based on this background, the investigators developed a smartphone app named TrackPAD to provide PAD-specific support for SET. The TrackPAD pilot study was designed as a 2-armed randomized controlled trial and included patients with diagnosed and symptomatic PAD. Patients were randomized by the Center for Clinical Studies in Essen using the TENALEA software into 2 groups. The control group included participants with standard care and no further mobile intervention. The intervention group included participants with standard care and additional mHealth-based self-tracking of their physical activity using trackPAD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
intervention group
Arm Type
Experimental
Arm Description
in addition to the usual therapy, the patients were given access to the trackPAD app
Arm Title
control group
Arm Type
No Intervention
Arm Description
patients in this group were treated as usual in the clinic without additional interventions.
Intervention Type
Device
Intervention Name(s)
trackPAD
Intervention Description
TrackPAD is a smartphone app to provide PAD-specific support for SET
Primary Outcome Measure Information:
Title
change in 6-minutes walking distance
Description
measured via GPS with the trackPAD app
Time Frame
baseline, 3 months follow-up
Secondary Outcome Measure Information:
Title
change in physical activity, measured in patients' self-report on how many days a week on average they engage in a physical activity that causes them to sweat or get out of breath, and how many minutes on average they spend doing it.
Description
to compare the two groups groups in terms of physical endurance, the self-reported physical activity was recorded
Time Frame
baseline, 3 months follow-up
Title
peripheral arterial disease-related quality of life
Description
measured with the Peripheral artery disease Quality of Life Questionnaire (PADQOL) questionnaire, a validated PAD-specific questionnaire. Minimum score is 38 and maximum is 228, with higher values indicating a better outcome.
Time Frame
baseline, 3 months follow-up
Title
Usability of the TrackPAD app
Description
measured with the User version of the Mobile Application Rating Scale (uMars) questionnaire. The uMARS includes 3 factors, namely app quality, app subjective quality and perceived impact. Minimum score of the app quality scale is 4 and the maximum is 20. The App Subjective Quality scale has a minimum of 4 and a maximum of 20, and the Perceived Impact scale has a minimum of 6 and a maximum of 30. Higher values indicate a better outcome.
Time Frame
baseline, 3 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of lower extremity PAD based on (and/or): ABI ≤ 0.9 in at least one legs Invasive or non-invasive imaging of stenotic lower extremity artery disease Endovascular or surgical revascularization of lower extremity artery PAD Fontaine Stage IIa/b Smartphone with possibility to use TrackPAD: Android ≥ 5.0 or IOS ≥ 11.0 Written informed consent prior to any study procedures, including a specified follow-up evaluation Best-medical treatment in the last 2 months in accordance with standard guidelines Exclusion Criteria: Wheelchair bound, use of walking aid or walking impairment due to another cause than PAD Below or above knee amputation Acute or critical limb ischemia PAD Fontaine Stage I or III / IV No German knowledge Severe cognitive dysfunction Congestive heart failure with NYHA III-IV symptoms Active congestive heart failure requiring the initiation or uptitration of diuretic therapy Angina pectoris with CCS class 3-4 symptoms or myocardial infarction or stroke in the last 3 months Active arrhythmia requiring the initiation or uptitration of anti-arrhythmic therapy Severe valve disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julia Lortz
Organizational Affiliation
University Hospital, Essen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiology and Vascular Medicine
City
Essen
ZIP/Postal Code
45147
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31244477
Citation
Paldan K, Simanovski J, Ullrich G, Steinmetz M, Rammos C, Janosi RA, Moebus S, Rassaf T, Lortz J. Feasibility and Clinical Relevance of a Mobile Intervention Using TrackPAD to Support Supervised Exercise Therapy in Patients With Peripheral Arterial Disease: Study Protocol for a Randomized Controlled Pilot Trial. JMIR Res Protoc. 2019 Jun 26;8(6):e13651. doi: 10.2196/13651.
Results Reference
background
PubMed Identifier
34398800
Citation
Paldan K, Steinmetz M, Simanovski J, Rammos C, Ullrich G, Janosi RA, Moebus S, Rassaf T, Lortz J. Supervised Exercise Therapy Using Mobile Health Technology in Patients With Peripheral Arterial Disease: Pilot Randomized Controlled Trial. JMIR Mhealth Uhealth. 2021 Aug 16;9(8):e24214. doi: 10.2196/24214.
Results Reference
derived

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Digital Support for Supervised Exercise Therapy in Peripheral Arterial Disease

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