← Back to Search

Exercise Programs for Knee Pain (SMARTSTEP Trial)

N/A
Recruiting
Led By Amit Shah, MD
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18-89 years
ABI < 0.9 after 10 minutes of rest
Must not have
Inability to attend study visits
Life-threatening process including unstable angina
Timeline
Screening 3 weeks
Treatment Varies
Follow Up over the 12-week study period
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing a smartphone-based exercise program with coaching against the usual care given by doctors. It aims to help patients with peripheral artery disease who often struggle to follow exercise routines. The smartphone program could make it easier for them to stay on track and improve their health.

Who is the study for?
This trial is for adults aged 18-89 with Peripheral Arterial Disease (PAD), who can consent and have specific Ankle-Brachial Index (ABI) or Toe-Brachial Index (TBI) scores indicating reduced blood flow. It's not for those whose walking is limited by other conditions, have life-threatening illnesses, severe heart failure, active behavioral issues that affect participation, or cannot attend study visits.
What is being tested?
The trial compares a smartphone-enabled structured exercise therapy program with coaching to the usual physician-directed exercise therapy. The goal is to see if using smartphones for guided exercises helps people with PAD better than standard advice from their doctors.
What are the potential side effects?
While the side effects are not detailed in this summary, typical risks may include discomfort from increased physical activity or potential injuries related to exercise. The smartphone app itself should not cause direct side effects.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am between 18 and 89 years old.
Select...
My ankle-brachial index is less than 0.9 after resting.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I cannot attend the study visits.
Select...
I have severe chest pain that is not stable.
Select...
I am currently experiencing a life-threatening condition like sepsis.
Select...
I have severe leg pain or wounds due to poor blood flow.
Select...
My life expectancy is less than 6 months due to my cancer.
Select...
I have severe heart failure.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~over the 12-week study period
This trial's timeline: 3 weeks for screening, Varies for treatment, and over the 12-week study period for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in 6-minute walk test (6MWT) distance completed
Secondary study objectives
Change in Physical Health Composite Score of SF-36
Change in Walking Impairment Questionnaire (WIQ) score
Change in ankle-brachial pressure index (ABPI)
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Smartphone-enabled structured exercise therapy (SE-SET)Experimental Treatment1 Intervention
This arm involves a smartphone app Movn - rehabilitation platform based on MULTIFIT, a case-management system for secondary prevention and patient surveillance after acute MI. The key features of the smartphone app include daily reminders to exercise, virtual diary for patients to enter data on exercise sessions, two-way secure messaging with the health coach, and educational videos on heart and vascular health.
Group II: Standard exercise therapyActive Control1 Intervention
Self-directed, unsupervised exercise as prescribed by the patient's physician.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Exercise therapy, including supervised and technology-assisted programs like smartphone-enabled exercise coaching, is a cornerstone treatment for Peripheral Arterial Disease (PAD). These programs work by improving blood flow and enhancing the efficiency of the muscles in the lower extremities, which helps to alleviate symptoms of claudication. Regular exercise promotes the development of collateral circulation, reduces inflammation, and improves endothelial function. For PAD patients, this means reduced pain, increased walking distance, and overall better quality of life. The use of technology, such as smartphone applications, can provide personalized coaching and motivation, making it easier for patients to adhere to their exercise regimen and achieve better outcomes.
Supervised exercise therapy versus non-supervised exercise therapy for intermittent claudication.

Find a Location

Who is running the clinical trial?

Woodruff Health Sciences Center FoundationUNKNOWN
1 Previous Clinical Trials
1,314 Total Patients Enrolled
Emory UniversityLead Sponsor
1,697 Previous Clinical Trials
2,603,868 Total Patients Enrolled
3 Trials studying Peripheral Arterial Disease
1,151 Patients Enrolled for Peripheral Arterial Disease
Amit Shah, MDPrincipal InvestigatorEmory University

Media Library

Peripheral Arterial Disease Research Study Groups: Smartphone-enabled structured exercise therapy (SE-SET), Standard exercise therapy
Peripheral Arterial Disease Clinical Trial 2023: Smartphone-enabled structured exercise therapy (SE-SET) Highlights & Side Effects. Trial Name: NCT03479255 — N/A
~1 spots leftby Jan 2025