Digital Support for Supervised Exercise Therapy in Peripheral Arterial Disease
TrackPAD
Supervised Exercise Therapy Using Mobile Health Technology in Patients With Peripheral Arterial Disease: Randomized Controlled Pilot Trial.
1 other identifier
interventional
40
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 6, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 28, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2019
CompletedFirst Submitted
Initial submission to the registry
June 9, 2021
CompletedFirst Posted
Study publicly available on registry
July 1, 2021
CompletedJuly 1, 2021
June 1, 2021
4 months
June 9, 2021
June 23, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
change in 6-minutes walking distance
measured via GPS with the trackPAD app
baseline, 3 months follow-up
Secondary Outcomes (3)
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.
baseline, 3 months follow-up
peripheral arterial disease-related quality of life
baseline, 3 months follow-up
Usability of the TrackPAD app
baseline, 3 months follow-up
Study Arms (2)
intervention group
EXPERIMENTALin addition to the usual therapy, the patients were given access to the trackPAD app
control group
NO INTERVENTIONpatients in this group were treated as usual in the clinic without additional interventions.
Interventions
TrackPAD is a smartphone app to provide PAD-specific support for SET
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Cardiology and Vascular Medicine
Essen, 45147, Germany
Related Publications (2)
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.
PMID: 31244477BACKGROUNDPaldan 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.
PMID: 34398800DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Julia Lortz
University Hospital, Essen
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
June 9, 2021
First Posted
July 1, 2021
Study Start
December 6, 2018
Primary Completion
March 28, 2019
Study Completion
April 30, 2019
Last Updated
July 1, 2021
Record last verified: 2021-06
Data Sharing
- IPD Sharing
- Will not share