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Static Muscular Stretching for Treatment of PAD

Primary Purpose

Peripheral Artery Disease

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ankle Splint
Sponsored by
Florida State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Peripheral Artery Disease

Eligibility Criteria

40 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 40+
  • A resting ankle-brachial index (ABI) of 0.90 or less in either leg
  • Stable disease (PAD) for a minimum of 3-months

Exclusion Criteria:

  • Habitual exercise (30 minutes of continuous activity for 3 or more days per week)
  • Cardiovascular rehabilitation program during the past 3 months
  • Below or above-knee amputation, critical limb ischemia (ulceration or gangrene)
  • Leg pain at rest
  • Cardiorespiratory disease
  • Diabetes
  • Major surgery or lower extremity revascularization during the previous 3 months
  • Major medical illness treatment during the prior 12 months
  • Central neurological disease
  • Limited ankle or knee joint range of motion
  • Requirement of oxygen with activity or exercise
  • More than a class II New York Heart Association level of heart failure
  • Wheelchair confinement, or inability to walk
  • Cognitive disorder
  • Vasculitis problem including Takayasu's arteritis, Buerger's disease, collagen disease or Raynaud's disease

Sites / Locations

  • Mayo Clinic FloridaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Stretch Group

No Stretch Group

Arm Description

Subjects assigned to this group will be instructed on how to wear the device to produce the appropriate amount of dorsiflexion (stretch). Splint devices will be worn at the assigned angle 5 days/week, 30 minutes/day, for 4 weeks. ABI, muscle oxygenation, and walking distance will be assessed pre/post stretching. Other health surveys will be administered.

Subjects assigned to this group will wear the splints but instructed to wear the device in a position that produces no stretch. Splint devices will be worn at the assigned angle 5 days/week, 30 minutes/day, for 4 weeks. ABI, muscle oxygenation, and walking distance will be assessed pre/post stretching. Other health surveys will be administered.

Outcomes

Primary Outcome Measures

Change in Muscle Oxygenation
Noninvasive assessment via NIRS monitor
Change in Continuous Walking Distance
Assessed by 6-minute walking test
Change in Total Walking Distance
Assessed by 6-minute walking test

Secondary Outcome Measures

Full Information

First Posted
January 7, 2020
Last Updated
February 22, 2023
Sponsor
Florida State University
Collaborators
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT04222751
Brief Title
Static Muscular Stretching for Treatment of PAD
Official Title
Static Muscular Stretching for Treatment of Peripheral Artery Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 29, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Florida State University
Collaborators
Mayo Clinic

4. Oversight

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

5. Study Description

Brief Summary
Patients with peripheral arterial disease (PAD) often have walking impairment due to insufficient oxygen supply to skeletal muscle. The investigator's pilot study in PAD patients has shown that endothelial function and walking distance improve with regular static muscle stretching. Therefore, the purpose of this study is to determine whether prescriptive muscle stretching improves muscle oxygenation and walking ability in PAD patients. This is a single-blinded study in 40 patients with stable symptomatic PAD. Patients assigned to the stretch group will use ankle splints (both legs) to perform static muscle stretching for 4 weeks (ankle dorsiflexion applied 30 min/d, 5 days/wk). Patients assigned to the control group will also wear the ankle splints daily but without invoking any dorsiflexion, i.e., without stretching. Measurements will consist of ankle-brachial index (ABI) at rest and post-exercise, skeletal muscle oxygenation (evaluated with near-infrared spectroscopy (NIRS)), and 6 minute walk test (6MWT), performed at baseline and after 4 weeks of stretching (or control splint placement). In addition, NIRS will be used to evaluate muscle oxygenation while patients are wearing the splint device in order to quantitatively prescribe the angle of dorsiflexion that provides optimum stretch and deoxygenation of the calf muscles without causing pain. Primary outcomes include increased muscle oxygenation during exercise and walking distance after 4 weeks of static muscle stretching. Results from this study will be used to support funding applications for a larger efficacy trial.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Stretch Group
Arm Type
Experimental
Arm Description
Subjects assigned to this group will be instructed on how to wear the device to produce the appropriate amount of dorsiflexion (stretch). Splint devices will be worn at the assigned angle 5 days/week, 30 minutes/day, for 4 weeks. ABI, muscle oxygenation, and walking distance will be assessed pre/post stretching. Other health surveys will be administered.
Arm Title
No Stretch Group
Arm Type
Placebo Comparator
Arm Description
Subjects assigned to this group will wear the splints but instructed to wear the device in a position that produces no stretch. Splint devices will be worn at the assigned angle 5 days/week, 30 minutes/day, for 4 weeks. ABI, muscle oxygenation, and walking distance will be assessed pre/post stretching. Other health surveys will be administered.
Intervention Type
Device
Intervention Name(s)
Ankle Splint
Intervention Description
Ankle splint will be slightly modified from the commercial form to include a pneumatic air cell secured under the forefoot below the splint's padded lining. This replaces the foam wedge provided by the manufacturer, allowing a gradual adjustment of the forefoot/toe region.
Primary Outcome Measure Information:
Title
Change in Muscle Oxygenation
Description
Noninvasive assessment via NIRS monitor
Time Frame
4 weeks
Title
Change in Continuous Walking Distance
Description
Assessed by 6-minute walking test
Time Frame
4 weeks
Title
Change in Total Walking Distance
Description
Assessed by 6-minute walking test
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 40+ A resting ankle-brachial index (ABI) of 0.90 or less in either leg Stable disease (PAD) for a minimum of 3-months Exclusion Criteria: Habitual exercise (30 minutes of continuous activity for 3 or more days per week) Cardiovascular rehabilitation program during the past 3 months Below or above-knee amputation, critical limb ischemia (ulceration or gangrene) Leg pain at rest Cardiorespiratory disease Diabetes Major surgery or lower extremity revascularization during the previous 3 months Major medical illness treatment during the prior 12 months Central neurological disease Limited ankle or knee joint range of motion Requirement of oxygen with activity or exercise More than a class II New York Heart Association level of heart failure Wheelchair confinement, or inability to walk Cognitive disorder Vasculitis problem including Takayasu's arteritis, Buerger's disease, collagen disease or Raynaud's disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Albert Hakaim, MD
Phone
904-953-2077
Email
hakaim.albert@mayo.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Mauricia Buchanan, RN
Phone
904-953-2077
Email
buchanan.mauricia@mayo.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Judy Delp, PhD
Organizational Affiliation
Florida State University, College of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emily Pritchard, PhD
Organizational Affiliation
Florida State University, College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Florida
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32224
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Albert Hakaim, MD
Phone
904-953-2077
Email
hakaim.albert@mayo.edu
First Name & Middle Initial & Last Name & Degree
Mauricia Buchanan, RN
Phone
904-953-2077
Email
buchanan.mauricia@mayo.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Static Muscular Stretching for Treatment of PAD

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