Implementation of Comprehensive Stroke Rehabilitation Therapy for Enhanced Quality of Life

University of Florida9 enrolled

Overview

The purpose of this research study is to implement into clinical practice, the comprehensive QualPro protocol for stroke survivors, which includes gait coordination, balance, mobility, and fitness training. Feasibility will be tested in the clinical environment by providing the intervention, measuring patient outcomes, and identifying the obstacles to insurance payment for the QualPro intervention. By productively addressing issues of implementation, the hypotheses of this study include proven feasibility in the clinical environment and clinically significant gains for stroke patients in the areas of strength, balance, gait coordination, endurance, physical function, and increased life role participation.

This comprehensive intervention targets the impairments preventing recovery to normal and safe gait, mobility, function, and life role participation (quality of life). It has been tested in chronic stroke survivors and found efficacious. The QualPro protocol will include three phases, all of which contain components previously mentioned. The QualPro protocol includes implementation of gait coordination training to address weakness, impaired endurance, and dyscoordination. The protocol will include implementation of balance training for falls prevention composed of Yang style, 24-posture, short-form Tai Chi. Additionally, the QualPro protocol will include implementation of aerobic training for fitness, health, and endurance of stroke survivors, which will be composed of low-volume, high intensity interval training (HIIT) on a cycle ergometer. Strength exercises will also be included. All exercises will address weakness, impaired endurance, and dyscoordination. The long-range financial goal of this research study is to realize the cost savings of implementing the proposed combination of interventions that will preclude much of the very costly and downwardly spiraling sequellae currently observed after stroke, and that currently costs managed care and insurance companies an exorbitant and unnecessary amount of precious resources.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

Interventions

Experimental Group, Sub-AcuteOTHER

For the sub-acute experimental group, the intervention schedule will be as follows: six months of individual therapy five times weekly (1 - 2.5 hours/session); 6 months of 'refresher' individual therapy twice monthly (1 - 2.5 hours/session) + group therapy up to three times weekly (1 hour/session); and 1 year of group therapy, up to three times weekly (1 hour/session) + 1 'refresher' individual therapy session every 3 months for a total study duration of 2 years.

Experimental Group, ChronicOTHER

For the chronic experimental group, the intervention schedule will be as follows: six months of individual therapy five times weekly (1 - 2.5 hours/session); 6 months of 'refresher' individual therapy twice monthly (1 - 2.5 hours/session) + group therapy up to three times weekly (1 hour/session); and 1 year of group therapy, up to three times weekly (1 hour/session) + 1 'refresher' individual therapy session every 3 months for a total study duration of 2 years.

Standard of Care, Sub-AcuteOTHER

This group will receive standard of care stroke rehabilitation therapy.

Standard of Care, ChronicOTHER

This group will receive standard of care stroke rehabilitation therapy.

Eligibility

Sex: ALLMin age: 21 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Cognition sufficiently intact to give valid informed consent to participate. * Sufficient endurance to participate in rehabilitation sessions. * Ability to follow 2 stage commands. * Medically stable * Age \> 21 years * Impaired ambulation as follows: inability to flex the knee and ankle in the sagittal plane, in a normal manner so the foot clears the floor; inability to control normal knee angle during single limb weight bearing during stance phase. * Trace contraction of hip, knee, and ankle flexors and extensors. * Passive range of motion (ROM) at hip, knee, ankle greater than or equal to normal gait kinematics. * Reported comfort of surface FES at a stimulus level producing a visible or palpable muscle contraction of ankle dorsiflexors. * Greater than 3 weeks post-stroke. * Living in the community and able to travel to training and assessment sites. * Approval of participation by primary care physician Exclusion Criteria: * Acute or progressive cardiac, renal, respiratory, neurological disorders or malignancy. * Active psychiatric diagnosis or psychological condition, or active drug/alcohol abuse. * Lower motor neuron damage or radiculopathy. * More than one stroke. * Cerebellar dysfunction. * Fugl-Meyer lower limb motor sub-score greater than 32. * Severe obesity (body mass index \> 35) * For the chronic group: current participation in physical therapy or cardiopulmonary rehabilitation. * Significant visual impairment affecting capability to gauge movement accuracy. * Current enrollment in any clinical trial * Planning to relocate out of the greater Gainesville, FL area during the study period * Unable to communicate sufficiently with study personnel * Clinical judgement regarding safety or non-compliance * Refusal to be recorded by video for gait assessment

Outcomes

Primary Outcomes

Patient response to QualPro intervention in the clinical environment

Implementation of the comprehensive QualPro protocol into clinical practice will be done in order to determine patient outcomes during interventions of gait coordination, balance, mobility, and fitness training.

Time frame: 24 months

Secondary Outcomes

Cost savings of implementation of the QualPro Protocol

Information with respect to the cost of standard care and cost of the proposed care model will be collected and compiled in order to determine feasibility in the clinical environment.

Time frame: 24 Months