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A STEP for Patients Prior to Undergoing TAVR: A Pilot Study (STEP)

Primary Purpose

Frail Elderly, Aortic Valve Stenosis

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Supervised TAVR Exercise Program
Sponsored by
OSF Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Frail Elderly focused on measuring Transcatheter Aortic Valve Disease, Supervised TAVR Exercise Program

Eligibility Criteria

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

Inclusion Criteria:

  • All adult patients scheduled to undergo first-time elective TAVR

Exclusion Criteria:

  • Vulnerable populations including prisoners, pregnant females and patients less than 18 years age.
  • Patients with history of unstable angina, myocardial infarction, or decompensated heart failure in the week prior to screening
  • Patients with physical limitations (i.e. debilitating stroke, amputation, unable to complete initial screening frailty profile)
  • Patients with advanced dementia or cognitive deficits (i.e. unable to follow instructions of initial screening frailty profile)
  • Exercise-induced arrhythmias

Sites / Locations

  • OSF St. Francis Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Supervised TAVR Exercise Program (STEP)

Standard of Care

Arm Description

Subjects in the experimental arm will participate in an individualized 4-week STEP prior to undergoing TAVR. All subjects will undergo serial frailty assessments by a blinded research assistant at baseline, pre-TAVR, and 30-days post-TAVR.

Subjects in the no intervention arm will proceed with their TAVR after a minimum 4 weeks without an exercise intervention. All subjects will undergo serial frailty assessments by a blinded research assistant at baseline, pre-TAVR, and 30-days post-TAVR.

Outcomes

Primary Outcome Measures

Change in Frailty Score from Baseline to post-STEP

Secondary Outcome Measures

Adverse Events
Change in Frailty Score from Baseline to 30-days post-TAVR
Change in Gait Speed (5-Meter Walk Test) from Baseline to post-STEP
Change in Gait Speed (5-Meter Walk Test) from Baseline to 30-days post-TAVR
Change in Grip Strength (Dynamometer) from Baseline to post-STEP
Change in Grip Strength (Dynamometer) from Baseline to 30-days post-TAVR
Change in Independent Activity (Katz Activities of Daily Living Survey) from Baseline to post-STEP
Change in Independent Activity (Katz Activities of Daily Living Survey) from Baseline to to 30-days post-TAVR
Change in Malnutrition (Serum Albumin Level) from Baseline to 30-days post-TAVR

Full Information

First Posted
April 28, 2016
Last Updated
April 10, 2018
Sponsor
OSF Healthcare System
Collaborators
HeartCare Midwest, University of Illinois College of Medicine at Peoria
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1. Study Identification

Unique Protocol Identification Number
NCT02766075
Brief Title
A STEP for Patients Prior to Undergoing TAVR: A Pilot Study
Acronym
STEP
Official Title
A Supervised TAVR Exercise Program (STEP) for Patients Prior to Undergoing Transcatheter Aortic Valve Replacement (TAVR): A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Terminated
Why Stopped
Low enrollment
Study Start Date
May 2016 (Actual)
Primary Completion Date
February 2018 (Actual)
Study Completion Date
February 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
OSF Healthcare System
Collaborators
HeartCare Midwest, University of Illinois College of Medicine at Peoria

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
The aim of this pilot study is to establish whether a Supervised TAVR Exercise Program (STEP) can safely improve the frailty status in patients with symptomatic severe aortic valve stenosis prior to undergoing transcatheter aortic valve replacement (TAVR).
Detailed Description
TAVR is an approved alternative therapy for patients with severe aortic valve stenosis who are deemed inoperable or high-risk for surgical aortic valve replacement (SAVR). Despite a very high procedural success rate (>95%), mortality rates after TAVR at 1- and 2-year follow-up remain ≥25% and ≥34%, respectively. It is becoming increasingly evident that frailty, as a clinical syndrome, has a large impact on this long term mortality. In a study by Green, et al. frailty status was independently associated with increased 1-year mortality (OR=3.5) after TAVR. The investigators' own retrospective analysis showed that impaired mobility and malnutrition were significantly associated with a longer hospital length of stay (5 days vs. 3 days), and increased total cost (on average, an additional $10,000 per patient). Given the phenotype of frailty is characterized by reductions in muscle mass, strength, endurance and activity level, a STEP is ideally suited to counteract these impairments. This pilot study aims to establish whether a STEP can safely improve the frailty score in patients with symptomatic severe aortic valve stenosis prior to undergoing TAVR. This single-center pilot study will be conducted in partnership between Heart Care Midwest (HCMW), OSF St. Francis Medical Center (OSF SFMC), and University of Illinois College of Medicine at Peoria (UICOMP). UICOMP Center of Outcomes Research will provide analytical support. The study will be funded by an operational research grant from OSF SFMC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frail Elderly, Aortic Valve Stenosis
Keywords
Transcatheter Aortic Valve Disease, Supervised TAVR Exercise Program

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Supervised TAVR Exercise Program (STEP)
Arm Type
Experimental
Arm Description
Subjects in the experimental arm will participate in an individualized 4-week STEP prior to undergoing TAVR. All subjects will undergo serial frailty assessments by a blinded research assistant at baseline, pre-TAVR, and 30-days post-TAVR.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Subjects in the no intervention arm will proceed with their TAVR after a minimum 4 weeks without an exercise intervention. All subjects will undergo serial frailty assessments by a blinded research assistant at baseline, pre-TAVR, and 30-days post-TAVR.
Intervention Type
Behavioral
Intervention Name(s)
Supervised TAVR Exercise Program
Intervention Description
Individualized exercise program designed and implemented by licensed physical therapy clinicians in three 60-minute sessions per week for four weeks. Upon randomization, subjects in the Intervention Group will undergo an initial Dynamic Gait & Balance Assessment by a licensed physical therapy clinician. The physical therapy clinician will use this assessment to design and implement an individualized STEP in three 60-minute sessions per week for four weeks. Subjects will proceed with their pre-TAVR testing in conjunction with the STEP sessions.
Primary Outcome Measure Information:
Title
Change in Frailty Score from Baseline to post-STEP
Time Frame
Baseline, 6-weeks
Secondary Outcome Measure Information:
Title
Adverse Events
Time Frame
6-weeks
Title
Change in Frailty Score from Baseline to 30-days post-TAVR
Time Frame
Baseline, 30-days post-TAVR
Title
Change in Gait Speed (5-Meter Walk Test) from Baseline to post-STEP
Time Frame
Baseline, 6-weeks
Title
Change in Gait Speed (5-Meter Walk Test) from Baseline to 30-days post-TAVR
Time Frame
Baseline, 30-days post-TAVR
Title
Change in Grip Strength (Dynamometer) from Baseline to post-STEP
Time Frame
Baseline, 6-weeks
Title
Change in Grip Strength (Dynamometer) from Baseline to 30-days post-TAVR
Time Frame
Baseline, 30-days post-TAVR
Title
Change in Independent Activity (Katz Activities of Daily Living Survey) from Baseline to post-STEP
Time Frame
Baseline, 6-weeks
Title
Change in Independent Activity (Katz Activities of Daily Living Survey) from Baseline to to 30-days post-TAVR
Time Frame
Baseline, 30-days post-TAVR
Title
Change in Malnutrition (Serum Albumin Level) from Baseline to 30-days post-TAVR
Time Frame
Baseline, 30-days post-TAVR

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All adult patients scheduled to undergo first-time elective TAVR Exclusion Criteria: Vulnerable populations including prisoners, pregnant females and patients less than 18 years age. Patients with history of unstable angina, myocardial infarction, or decompensated heart failure in the week prior to screening Patients with physical limitations (i.e. debilitating stroke, amputation, unable to complete initial screening frailty profile) Patients with advanced dementia or cognitive deficits (i.e. unable to follow instructions of initial screening frailty profile) Exercise-induced arrhythmias
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay N Patel, MD
Organizational Affiliation
OSF Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
OSF St. Francis Medical Center
City
Peoria
State/Province
Illinois
ZIP/Postal Code
61630
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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A STEP for Patients Prior to Undergoing TAVR: A Pilot Study

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