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Game-Based Foot & Ankle Exercise for Those With Lower Extremity Edema

Primary Purpose

Lower Extremity Swelling, Lower Extremity Edema, Venous Insufficiency of Leg

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Game-based exercise
Sponsored by
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Lower Extremity Swelling focused on measuring Compression Garment, Game-based Exercise

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients (18+ years old) who have lower extremity edema
  • Willing to attend clinic for assessments

Exclusion Criteria:

  • Severe cognitive decline that reduces their ability to use tele-foot exercise device
  • Major visual problems that reduces their ability to use tele-foot exercise device
  • Inability to walk independently for a distance of 10 meters
  • Major foot problems such as active lower extremity wounds
  • Major foot deformity (e.g., Charcot Foot)
  • Previous major amputations, and claudication
  • Decompensated or advanced heart failure New York Heart Association (NYHA) Functional Class(FC) III-IV
  • Significant heart disease

Sites / Locations

  • Baylor College of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Active group (AG)

Control group (CG)

Arm Description

Active group (AG). The AG (n=15) will play game-based foot and ankle exercises via a mobile application on a tablet. They will be asked to wear a foot sensor that is connected to the tablet during the exercise. They will be asked to play the game for 5-minutes, daily. They will do this in conjunction with wearing a compression garment for a period of 4 weeks.

Control Group (CG). The CG (n=15) will wear a compression garment for four weeks.

Outcomes

Primary Outcome Measures

Change in calf circumference from baseline to 4 weeks
Calf circumference will be assessed with a soft measuring tape for each leg
Change in foot circumference from baseline to 4 weeks
Foot circumference will be assessed with a soft measuring tape for each leg
Change in foot volume from baseline to 4 weeks
Foot volume will be assessed with a standard foot volumeter
Change in pitting edema grade from baseline to 4 weeks
Coordinators will press on the affected area in the lower extremities and measure depth of indention. They will record the length of skin rebound time and grade the edema based on validated scales

Secondary Outcome Measures

Change in gastrocnemius muscle strength from baseline to 4 weeks
Lower extremity strength will be assessed with an ankle dynamometer and surface electromyography (Delsys Trigno Wireless EMG System, MA, US).
Change in gait and balance from baseline to 4 weeks
Gait speed will be measured with standard walking tests and wearable sensors (Legsys).
Change in balance from baseline to 4 weeks
Static balance will be measured with standard balance tests and wearable sensors (Balansens).
Change in plantar tissue oxygen saturation/consumption from baseline to 4 weeks
Percentage of tissue oxygen saturation (SatO2) and hemoglobin values will be measured using a validated near-infrared (NIR) camera (Snapshot NIR, KENT Imaging Inc., Calgary, AB, Can) that detects an approximate value of real-time SatO2 and level in superficial tissue. The area that will be captured is the metatarsus area

Full Information

First Posted
August 26, 2022
Last Updated
February 8, 2023
Sponsor
Baylor College of Medicine
Collaborators
Medline Industries
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1. Study Identification

Unique Protocol Identification Number
NCT05520008
Brief Title
Game-Based Foot & Ankle Exercise for Those With Lower Extremity Edema
Official Title
A Game-based Foot & Ankle Exercise Program to Increase Efficacy Of Compression Garments At Managing Edema
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 3, 2022 (Actual)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
September 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baylor College of Medicine
Collaborators
Medline Industries

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 present study aims to use a game-based tele-exercise program for patients using a compression garment to improve lower extremity edema. This tele-exercise gaming platform can work as an efficient exercise to improve patients' muscle strength. It also can be helpful in improving edema and venous return and can be used in addition to compression garments to increase efficacy. The sample size (n=30) is convenient and designed to explore acceptability and feasibility. Eligible participants will be screened at the Baylor college of Medicine Clinic based on the inclusion/exclusion criteria. Participants who satisfy the inclusion and exclusion criteria and sign the informed consent form will be randomly assigned with ratio of 1:1 into two groups. Both groups will receive a compression garment to use for 4 weeks, and in the intervention group, patients will receive a sensor and a tablet to play foot & ankle exercise games twice a day for 5 minutes. Study participation will be 4 weeks for all participants. Participants will be assessed in two visits: a baseline visit (BL) and a visit at the end of the 4 weeks (W4). The primary outcomes will be calf circumference, foot volume, and pitting edema grade. Secondary outcomes include limb strength, foot perfusion, gait assessment (gait speed, stride length, double stance, and gait steadiness), balance, and quality of life. The coordinator will monitor patients weekly to see their adherence to the compression garment and game-based exercise.
Detailed Description
Lower extremity edema (LE) is an accumulation of interstitial fluid volume in the legs and feet and commonly occurs in patients with diabetes, hypertension, kidney disease, heart failure, cirrhosis, cancer, and obesity. LE can also result from deep vein thrombosis (DVT) in the lower leg. Compression socks or garments are often used to decrease this edema. Despite the efficacy of this treatment, there are some limitations including low patient compliance and contraindication of high compression levels for patients with high grades of peripheral arterial disease. Given that it is has previously been shown that exercise can be a positive way to reduce LE, the present study aims to use a game-based exercise program to help increase patient's movement and thus improve efficacy and adherence to the compression garments/socks. The investigators will recruit 30 participants and randomly divide them into two groups: Active Group (AG) and Control Group (CG). Both groups will receive a compression garment (CompreCares) developed by Medline Incorporated(Inc). (IL, USA). The AG will receive a tablet and foot sensor (TEXASSENSE INC, USA), and will be instructed to play with it daily for 5 minutes over the period of 4 weeks. During the two study visits (BL and W4), the investigators will assess the following outcomes: calf muscle activation (assessed by surface electromyography [sEMG]), foot perfusion (SNAPSHOT NIR, Kent Imaging System), calf and foot circumference, ankle-brachial index (ABI), pitting edema test, foot volume, gait, balance, and peripheral neuropathy (DPNCheck, Neurometrix Inc., Woburn, Massachusetts, USA). Acceptability and patient reported outcomes will be assessed via validated questionnaires collected at each study visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lower Extremity Swelling, Lower Extremity Edema, Venous Insufficiency of Leg
Keywords
Compression Garment, Game-based Exercise

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants who satisfy the inclusion and exclusion criteria and sign the informed consent form will be randomly assigned with a ratio of 1:1 into two groups. Both groups will be given a compression garment (CompreCares, Medline, IL, USA) to wear for the 4 weeks of the study. The Active group (AG) will also be allocated a tablet and foot sensor so that they can play game-based foot & ankle exercises during the same time period. The other group (Control group, CG) will only use the compression garment.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active group (AG)
Arm Type
Experimental
Arm Description
Active group (AG). The AG (n=15) will play game-based foot and ankle exercises via a mobile application on a tablet. They will be asked to wear a foot sensor that is connected to the tablet during the exercise. They will be asked to play the game for 5-minutes, daily. They will do this in conjunction with wearing a compression garment for a period of 4 weeks.
Arm Title
Control group (CG)
Arm Type
No Intervention
Arm Description
Control Group (CG). The CG (n=15) will wear a compression garment for four weeks.
Intervention Type
Other
Intervention Name(s)
Game-based exercise
Other Intervention Name(s)
Tele-exercise
Intervention Description
Patients in the active group will put on a sensor connected to a tablet to play a game-based foot/ankle exercise twice a day for 5 minutes for four weeks.
Primary Outcome Measure Information:
Title
Change in calf circumference from baseline to 4 weeks
Description
Calf circumference will be assessed with a soft measuring tape for each leg
Time Frame
4 weeks from baseline
Title
Change in foot circumference from baseline to 4 weeks
Description
Foot circumference will be assessed with a soft measuring tape for each leg
Time Frame
4 weeks from baseline
Title
Change in foot volume from baseline to 4 weeks
Description
Foot volume will be assessed with a standard foot volumeter
Time Frame
4 weeks from baseline
Title
Change in pitting edema grade from baseline to 4 weeks
Description
Coordinators will press on the affected area in the lower extremities and measure depth of indention. They will record the length of skin rebound time and grade the edema based on validated scales
Time Frame
4 weeks from baseline
Secondary Outcome Measure Information:
Title
Change in gastrocnemius muscle strength from baseline to 4 weeks
Description
Lower extremity strength will be assessed with an ankle dynamometer and surface electromyography (Delsys Trigno Wireless EMG System, MA, US).
Time Frame
4 weeks from baseline
Title
Change in gait and balance from baseline to 4 weeks
Description
Gait speed will be measured with standard walking tests and wearable sensors (Legsys).
Time Frame
4 weeks from baseline
Title
Change in balance from baseline to 4 weeks
Description
Static balance will be measured with standard balance tests and wearable sensors (Balansens).
Time Frame
4 weeks from baseline
Title
Change in plantar tissue oxygen saturation/consumption from baseline to 4 weeks
Description
Percentage of tissue oxygen saturation (SatO2) and hemoglobin values will be measured using a validated near-infrared (NIR) camera (Snapshot NIR, KENT Imaging Inc., Calgary, AB, Can) that detects an approximate value of real-time SatO2 and level in superficial tissue. The area that will be captured is the metatarsus area
Time Frame
4 weeks from baseline
Other Pre-specified Outcome Measures:
Title
Change in peripheral neuropathy from baseline to 4 weeks
Description
Peripheral neuropathy will be assessed using DPNCheck (Neurometrix, Woburn, MA, USA). This is a noninvasive device which will measure conduction velocity and amplitude.
Time Frame
4 weeks from baseline
Title
Patient acceptance at 4 weeks
Description
Participant acceptance of the tele-exergaming program will be assessed at the end of their participation using a validated technology acceptance model (TAM) questionnaire
Time Frame
4 weeks from baseline
Title
Change in physical activity (step count and intensity minutes) from baseline to 4 weeks
Description
Physical activity metrics, such as step count and intensity minutes, will be measured over the course of the 4 weeks using a smart watch (Vivosmart 4, Garmin, US)
Time Frame
4 weeks from baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (18+ years old) who have lower extremity edema Willing to attend clinic for assessments Exclusion Criteria: Severe cognitive decline that reduces their ability to use tele-foot exercise device Major visual problems that reduces their ability to use tele-foot exercise device Inability to walk independently for a distance of 10 meters Major foot problems such as active lower extremity wounds Major foot deformity (e.g., Charcot Foot) Previous major amputations, and claudication Decompensated or advanced heart failure New York Heart Association (NYHA) Functional Class(FC) III-IV Significant heart disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bijan Najafi, Najafi
Phone
713-798-7538
Email
bijan.najafi@bcm.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Noun, BS
Phone
7137987538
Email
maria.noun@bcm.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bijan Najafi, PhD
Organizational Affiliation
Baylor College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bijan Najafi, PhD
Phone
713-798-7538
Email
bijan.najafi@bcm.edu
First Name & Middle Initial & Last Name & Degree
Maria Noun, BS
Phone
7137987538
Email
maria.noun@bcm.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Game-Based Foot & Ankle Exercise for Those With Lower Extremity Edema

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