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Physical Activity Interventions for Leg Ulcer Patients (FOOTFIT)

Primary Purpose

Leg Ulcers, Venous Ulcers, Varicose Ulcers

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
FOOTFIT
Sponsored by
Medical University of South Carolina
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Leg Ulcers

Eligibility Criteria

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

Inclusion Criteria:

  • Active venous leg ulcer
  • Ankle brachial index 0.80 to 1.3 mmHg, a measure of arterial sufficiency
  • Sedentary-able to only walk a few steps at a time or not farther than 10 feet
  • Not currently exercising or participate in a PA or physical therapy program
  • Receives at least weekly wound care anticipated to last for at least six weeks from start of study
  • Able to don accelerometer - if unable to apply independently, has assistance from other
  • Capable of using Smartphone

Exclusion Criteria:

  • Co-morbid conditions such as stroke (limits ankle function)
  • Ulcer from other causes (arterial, diabetic, trauma, surgery)
  • Documented cognitive impairment (MiniCog)
  • No 3G service in area where patient resides

Sites / Locations

  • Spartanburg Regional Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

FOOTFIT Plus

FOOTFIT

Arm Description

The intervention consists of: 1) a prescribed, evidence-based, phased, non-exertive physical activity conditioning activities for lower leg function (CALF) movements that are to be performed daily at home; 2) a low-cost, tri-axial Bluetooth® enabled highly sensitive motion-sensing accelerometer and tracking device (BEAT) worn on the foot during CALF to capture frequency and intensity of foot movements; and 3) a Smartphone that receives foot movement data, provides automated educational/motivational messages, and reports and allows regular communication with the wound care provider on progress.

The intervention consists of: 1) a prescribed, evidence-based, phased, non-exertive physical activity conditioning activities for lower leg function (CALF) movements that are to be performed daily at home; 2) a low-cost, tri-axial Bluetooth® enabled highly sensitive motion-sensing accelerometer and tracking device (BEAT) worn on the foot during CALF to capture frequency and intensity of foot movements; and 3) a Smartphone that receives foot movement data, provides automated educational/motivational messages, and reports. There is not regular communication with the wound care provider on progress.

Outcomes

Primary Outcome Measures

FOOTFIT feasibility
Measure adherence by recording frequency and intensity of foot/toe movements reported in minutes.
FOOTFIT reach
Measure reach, recorded as qualitative documents on a log of how patients learned about the study.
FOOTFIT technology implementation procedures
Record on study log the number and types of problems encountered with the study nurses teaching participants to use the foot accelerometer technology, the number and types problems reported by patient, the number and types of recommendations made by the participant regarding the use of the accelerometer, and nurse or provider recommendations for changes to refine the foot accelerometer technology, and the number and types of refinements to the technology that were made.
FOOTFIT acceptability
Record on study logs the the number (frequency) and types of interactions such as phone calls, emails or texts, between the patient and provider regarding FOOTFIT+ including reasons (i.e., exercises, adverse events that are related to, and not related to the use of the accelerometer).

Secondary Outcome Measures

Efficacy on pain
Obtain estimates of variability for short-term functional impacts on pain using the numerical rating scale (NRS) as a single score.
Efficacy on foot strength
Obtain estimates of variability for short-term functional impacts on foot strength using the dynamometer and reported as pounds per square inch.
Efficacy on foot range of motion.
Obtain estimates of variability for short-term functional impacts on foot range of motion using the goniometer and reported in degrees.
Efficacy on walking function.
Obtain estimates of variability for short-term functional impacts on walking function using the Foot and Ankle Ability Measure and reported as a sum score.
Efficacy on walking performance
The Six Minute Walk Test reported as distance in feet over six minutes time.

Full Information

First Posted
December 1, 2015
Last Updated
September 5, 2018
Sponsor
Medical University of South Carolina
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1. Study Identification

Unique Protocol Identification Number
NCT02632695
Brief Title
Physical Activity Interventions for Leg Ulcer Patients
Acronym
FOOTFIT
Official Title
Physical Activity Interventions for Leg Ulcer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
August 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to test FOOTFIT and enhanced FOOTFIT+, home-based mobile health (mHealth) physical activity (PA) interventions for a minimally ambulatory, chronically-ill, population with leg ulcers. A highly sensitive clinically designed Bluetooth® enabled accelerometer and tracking device (BEAT) worn on the foot during a progressive and evidence-based non-exertive leg conditioning activities for lower leg function (CALF) captures minute foot movements and sends the data to a Smartphone. This six-week feasibility study will compare FOOTFIT to FOOTFIT+, with the added connectivity feature, to promote patient-provider communication, evaluate adherence to PA, and assess signals of efficacy on functional outcomes in a very low fitness population.
Detailed Description
FOOTFIT is a study of a lower leg conditioning mHealth intervention for patients with venous leg ulcers. The aims are to compare two versions, one of which is enhanced (FOOTFIT+), to determine which has the greatest impact on physical activity adherence, patient-provider communication, and leg function. FOOTFIT and FOOTFIT+ share three components: 1) a low-cost, tri-axial Bluetooth® enabled highly sensitive accelerometer and tracking device (BEAT) worn on the foot during, 2) phased conditioning activities for lower leg function (CALF) tracked by a, 3) Smartphone that captures signals from BEAT, provides motivational messages, CALF instruction, and automated feedback on progress. Forty patients will be targeted in this six-week study, 20 of which will receive FOOTFIT and 20 FOOTFIT+.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leg Ulcers, Venous Ulcers, Varicose Ulcers

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FOOTFIT Plus
Arm Type
Experimental
Arm Description
The intervention consists of: 1) a prescribed, evidence-based, phased, non-exertive physical activity conditioning activities for lower leg function (CALF) movements that are to be performed daily at home; 2) a low-cost, tri-axial Bluetooth® enabled highly sensitive motion-sensing accelerometer and tracking device (BEAT) worn on the foot during CALF to capture frequency and intensity of foot movements; and 3) a Smartphone that receives foot movement data, provides automated educational/motivational messages, and reports and allows regular communication with the wound care provider on progress.
Arm Title
FOOTFIT
Arm Type
Experimental
Arm Description
The intervention consists of: 1) a prescribed, evidence-based, phased, non-exertive physical activity conditioning activities for lower leg function (CALF) movements that are to be performed daily at home; 2) a low-cost, tri-axial Bluetooth® enabled highly sensitive motion-sensing accelerometer and tracking device (BEAT) worn on the foot during CALF to capture frequency and intensity of foot movements; and 3) a Smartphone that receives foot movement data, provides automated educational/motivational messages, and reports. There is not regular communication with the wound care provider on progress.
Intervention Type
Device
Intervention Name(s)
FOOTFIT
Intervention Description
Individuals with venous leg ulcers will be instructed on physical activity movements for their lower legs to be performed over six weeks while wearing a foot based activity monitor (accelerometer) that will send them motivational messages and progress reports. For those in the FOOTFIT Plus group, individuals will have the option to communicate with their wound care provider via text messages, emails or phone calls.
Primary Outcome Measure Information:
Title
FOOTFIT feasibility
Description
Measure adherence by recording frequency and intensity of foot/toe movements reported in minutes.
Time Frame
6 weeks
Title
FOOTFIT reach
Description
Measure reach, recorded as qualitative documents on a log of how patients learned about the study.
Time Frame
6 weeks
Title
FOOTFIT technology implementation procedures
Description
Record on study log the number and types of problems encountered with the study nurses teaching participants to use the foot accelerometer technology, the number and types problems reported by patient, the number and types of recommendations made by the participant regarding the use of the accelerometer, and nurse or provider recommendations for changes to refine the foot accelerometer technology, and the number and types of refinements to the technology that were made.
Time Frame
6 weeks
Title
FOOTFIT acceptability
Description
Record on study logs the the number (frequency) and types of interactions such as phone calls, emails or texts, between the patient and provider regarding FOOTFIT+ including reasons (i.e., exercises, adverse events that are related to, and not related to the use of the accelerometer).
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Efficacy on pain
Description
Obtain estimates of variability for short-term functional impacts on pain using the numerical rating scale (NRS) as a single score.
Time Frame
6 weeks
Title
Efficacy on foot strength
Description
Obtain estimates of variability for short-term functional impacts on foot strength using the dynamometer and reported as pounds per square inch.
Time Frame
6 weeks
Title
Efficacy on foot range of motion.
Description
Obtain estimates of variability for short-term functional impacts on foot range of motion using the goniometer and reported in degrees.
Time Frame
6 weeks
Title
Efficacy on walking function.
Description
Obtain estimates of variability for short-term functional impacts on walking function using the Foot and Ankle Ability Measure and reported as a sum score.
Time Frame
6 weeks
Title
Efficacy on walking performance
Description
The Six Minute Walk Test reported as distance in feet over six minutes time.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active venous leg ulcer Ankle brachial index 0.80 to 1.3 mmHg, a measure of arterial sufficiency Sedentary-able to only walk a few steps at a time or not farther than 10 feet Not currently exercising or participate in a PA or physical therapy program Receives at least weekly wound care anticipated to last for at least six weeks from start of study Able to don accelerometer - if unable to apply independently, has assistance from other Capable of using Smartphone Exclusion Criteria: Co-morbid conditions such as stroke (limits ankle function) Ulcer from other causes (arterial, diabetic, trauma, surgery) Documented cognitive impairment (MiniCog) No 3G service in area where patient resides
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Moby Madisetti, MS
Organizational Affiliation
Medical University of South Carolina
Official's Role
Study Director
Facility Information:
Facility Name
Spartanburg Regional Medical Center
City
Spartanburg
State/Province
South Carolina
ZIP/Postal Code
29303
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32412419
Citation
Kelechi TJ, Prentice MA, Mueller M, Madisetti M, Vertegel A. A Lower Leg Physical Activity Intervention for Individuals With Chronic Venous Leg Ulcers: Randomized Controlled Trial. JMIR Mhealth Uhealth. 2020 May 15;8(5):e15015. doi: 10.2196/15015.
Results Reference
derived

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Physical Activity Interventions for Leg Ulcer Patients

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