Metabolic Costs of Walking Post Stroke

NCT ID: NCT02108912

Last Updated: 2019-03-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-03-31
• Study Completion Date: 2017-01-31

Brief Summary

This will be a randomized, matched-group study to compare the cardiopulmonary / metabolic benefits for persons post stroke that learn to walk utilizing early treadmill training post-acute stroke to persons post stroke that learn to walk utilizing non-treadmill based gait training during the same time period. Participants (n=30) will be adults who have completed acute rehabilitation following a stroke. Random assignment will be to either the ESTT or traditional gait training protocol during the outpatient rehabilitation phase.

1. Group A: Traditional outpatient therapy (n = 15)

2. Group B: Treadmill training (ESTT) outpatient therapy (n = 15)

Detailed Description

At the time of enrollment, participants will be randomly assigned to one of the two groups depending on the severity of impairment in the hemiparetic lower extremity. Groups will be matched based on high functioning vs. low functioning (STREAM scores). Group assignment will be done by random drawing from concealed envelopes with red or blue chips for assignment to ESTT or non-treadmill based outpatient therapy services. For the next participant who is screened with a similar STREAM impairment level, he/she will be placed in the alternate group to match the group assignments. Enrollment will proceed in this fashion. All outpatient therapy services will be provided at the UT Southwestern School of Health Professions School of Physical Therapy Gait Disorders Clinic (UTSW GDC). The groups will be as follows:

1. Group A: Traditional outpatient therapy (n = 15)

2. Group B: Treadmill (ESTT) outpatient therapy (n = 15) Therapy for the purposes of the study will be discontinued after a maximum of 24 training sessions or 8 weeks. It is anticipated, based on the research concerning AFO use in persons with stroke, that all participants will require an AFO for safe gait training in the outpatient setting.

Traditional outpatient therapy: For persons in Group A, gait training will consist of 30 minutes of walking training. The program may include a variety of interventions that are commonly done to rehabilitate gait after stroke (excluding treadmill training). Walking may include the use of various assistive devices such as rolling walkers, gait trainers, canes and crutches. Other tools that may be utilized include visual cues (tape, lasers) and auditory cues (metronome). Other activities such as single limb stance and stair climbing may be included to facilitate limb stability. Functional electrical stimulation (FES) may be used to facilitate muscle activation in the hemiparetic lower extremity during gait training for all participants. Stimulation may be applied to muscles of the upper and/or lower leg gait training. Use of electrical stimulation will be documented, including all parameters (make and model of unit, rate of stimulation [pulses per second], waveform, and duration of use). Appropriate exercises from a bank of exercises will be selected for each participant. The bank of exercises will include: standing heel cord stretches, single leg stance, sit to stand, timed standing, marching in place, tap ups, step ups, step throughs, standing ball roll, stair climbing, standing Theraband exercises, wall squats. They will be advised to complete the exercises daily (5 days/week total) for a total of 30 minutes per day. In addition, they will be instructed to wear the AFO for all upright mobility tasks, in combination with the prescribed assistive device.

Treadmill (ESTT) outpatient therapy: For persons in Group B, study-related outpatient gait training will be initiated on the treadmill with partial body weight support. The initial body weight support will be set between 30% and 50% of patient's body weight. During progressive training sessions, the amount of body weight support will attempt to be reduced and the researcher will assess the response to the increased body weight on the gait pattern. The initial speed of the treadmill will be 0.7 mph (minimum initial speed) and will be increased progressively as tolerated until a speed of 1.8 mph is reached. Subject tolerance to the intervention will be monitored closely. Gait training on the treadmill will be scheduled in 30-minute sessions. The subjects will be allowed to take rest breaks as needed during the treadmill training.

During gait training on the treadmill, ankle control will be facilitated by means of an ankle foot orthosis (AFO) with a double adjustable joint. For over ground gait, participants will also use an AFO with a double adjustable joint Functional electrical stimulation (FES) may be used to facilitate muscle activation in the hemiparetic lower extremity during gait training for all participants. Over ground gait will not be initiated until the subject is able to walk on the treadmill with no more than 10% body weight support and with no more than minimal assist to advance the hemiparetic leg at a speed of 0.8 mph or greater for at least 3 minutes for two consecutive bouts. (Subjects can also have assistance with weight shift.) Once over ground gait is initiated, either bilateral or unilateral support will be used, depending on upper extremity control and general upright stability. If the quality of the gait deteriorates significantly from the gait observed on the treadmill, over ground gait will be halted for that session. Treadmill training will continue to progress to over ground gait. Once over ground gait training is initiated, 20 minutes of the 30 total therapy minutes will be spent on treadmill training and 10 minutes will be spent on over ground gait training. Treadmill training will continue until subjects are able to walk 10 minutes without resting with no body weight support, but with vest on for safety, without upper extremity support without assist for weight shift or lower extremity control at a speed of 1.8 mph. If this is prior to the conclusion of study-related therapy, the entire 30 minute session will be spent practicing over ground gait.

Appropriate exercises from a bank of exercises will be selected for each participant. The bank of exercises will include: standing heel cord stretches, single leg stance, sit to stand, timed standing, marching in place, tap ups, step ups, step throughs, standing ball roll, stair climbing, standing Theraband exercises, wall squats. They will be advised to complete the exercises daily (5 days/week total) for a total of 30 minutes per day. In addition, they will be instructed to wear the AFO for all upright mobility tasks, in combination with the prescribed assistive device.

The Step Program: To introduce this component of the study, the participant and caregiver/support person will be given a 15-minute presentation entitled Step it Up. This program was developed by the research team and it addresses the critical need and benefits of exercise for persons post stroke, methods of safe exercise monitoring and information on progression of exercise intensity and duration to improve cardiorespiratory function. The presentation will include an explanation of the Borg Rate of Perceived Exertion (RPE, 6-20 scale) and directions on how to utilize a pedometer for daily walking measurement. Following the presentation, participants will meet with an investigator and demonstrate competency with the application of the pedometer and utilization of the RPE scale. Each participant will be provided written material that covers the salient points of the presentation. They will also receive a notebook that has the instructions along with 16 weekly logs for recording walking data. The training should take approximately 30 minutes and will take place following the final gait treatment.

The walking program will continue until T4 and T4a. Each participant will be scheduled for this testing within 10 calendar days of the 24-week anniversary of the commencement of outpatient therapy. At this testing time (T4 & T4a) all outcome measures will be repeated. The final testing time (T5 and T5 a) will be completed within 10 calendar days of 288-day anniversary of commencement of outpatient physical therapy. All outcome measures will be repeated at this testing time. This will be the termination point of the study.

Conditions

Acute Stroke

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Traditional outpatient

Traditional outpatient physical therapy

Group Type: EXPERIMENTAL

Traditional outpatient

Intervention Type: OTHER

Traditional physical therapy includes standard of care for gait recovery after stroke such as pre-gait activities, standing balance activities, strengthening, walking with assistive devices.

ESTT outpatient

ESTT (early standardized task-specific training) in outpatient rehabilitation

Group Type: EXPERIMENTAL

ESTT

Intervention Type: OTHER

ESTT is early-standardized task-specific training is a treadmill and over ground gait protocol for gait recovery after stroke

Interventions

ESTT

ESTT is early-standardized task-specific training is a treadmill and over ground gait protocol for gait recovery after stroke

Intervention Type: OTHER

Traditional outpatient

Traditional physical therapy includes standard of care for gait recovery after stroke such as pre-gait activities, standing balance activities, strengthening, walking with assistive devices.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• confirmed diagnosis of recent cerebrovascular accident (CVA) (less than 6 weeks post at the time of admission to inpatient rehabilitation)
• able to give informed consent independently or have family member or other authorized surrogate available to give consent
• first time stroke OR complete gait recovery from prior stroke
• sufficient support at home to participate in home-based fitness training program
• transportation to University of Texas Southwestern Medical Center Gait Disorders Clinic (UTSW GDC) for therapy and testing
• ability to follow one-part commands

Exclusion Criteria

• non-ambulatory before onset of stroke (at time of admission to inpatient rehabilitation)
• bilateral stroke
• presence of severe cardiac problems (heart failure [New York Heart Association > Class 2], unstable or exercise-induced angina)
• other co-morbidities which could affect gait training (i.e. amputation, spinal cord injury, traumatic brain injury, etc.)
• recent myocardial infarct (within 4 weeks of date of inpatient rehabilitation admission)
• any uncontrolled health condition for which exercise is contraindicated
• severe lower extremity joint disease/pathology that would interfere with gait training
• subjects -with body mass index (BMI) greater than 40
• significant cognitive impairment (less than 2 on the Functional Independence Measure [FIM] cognitive sub-scale)
• age greater than 80 years or less than 18 years
• able to complete 5 or more full heel raises with the affected ankle in standing with the knee extended with no more than one or two fingers on support surface for balance

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Texas Southwestern Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Karen J McCain, DPT

Role: PRINCIPAL_INVESTIGATOR

UT Southwestern Medical Center

Locations

UT Southwestern School of Health Professions

Dallas, Texas, United States

Countries

United States

Other Identifiers

AHA Award #14CRP18500016

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

AHA CV study

Identifier Type: -

Identifier Source: org_study_id