Effect of Lyra Gait Training on the Mobility of Geriatric Rehabilitation Inpatients
Primary Purpose
Mobility Limitation, Muscle Weakness
Status
Terminated
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Gait training with the THERA-Trainer Lyra
Physical therapy
Sponsored by
About this trial
This is an interventional treatment trial for Mobility Limitation focused on measuring gait, mobility, geriatric, rehabilitation, inpatient
Eligibility Criteria
Inclusion Criteria:
- 65 years of age or older
- Rehabilitation inpatients at Felix Platter Hospital with primarily muscle weakness and difficulty walking
- Community-dwellers before hospital admission with planned discharge home
- Body weight 150 kg or less
- Body height between 100 cm and 195 cm
- Mini-Mental State Examination score 21 points or more
- Signed informed consent for study participation
Exclusion Criteria:
- Clinically significant neurologic or musculoskeletal diseases which severly affect walking, e.g. advanced Parkinson's disease or hemiplegia
- Severe cardiac insufficiency
- Advanced chronic pulmonary disease (COPD Gold IV)
- Amputations of extremities (except missing fingers)
- Blindness
- Inability to understand and speak German well enough to understand the patient information, training and assessment instructions
Sites / Locations
- Felix Platter Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intervention Group
Control Group
Arm Description
Gait training with the THERA-Trainer Lyra (3x/week) in addition to conventional geriatric rehabilitation physical therapy (6x/week) during inpatient period. After discharge home, continuation of Lyra gait training (3x/week), discontinuation of physical therapy.
Conventional geriatric rehabilitation physical therapy (6x/week) during inpatient period. After discharge home, discontinuation of physical therapy.
Outcomes
Primary Outcome Measures
Change in gait velocity
Habitual, preferred ("normal") walking speed (cm/s) quantified with the GAITRite electronic walkway system
Secondary Outcome Measures
Change in grip strength
Grip strength (kg) of each hand (best result of two attempts for each hand used for data analysis)
Change in general mobility
Timed Up and Go Test time (seconds); faster test times represent better general mobility
Change in spatial-temporal gait parameters (other than walking velocity)
Gait parameters quantified with the GAITRite electronic walkway system
Change in endurance
Six Minute Walk Test; distance walked (meters) in six minutes; greater distance walked represents better endurance
Change in functionality (DEMMI total score, absolute values)
The de Morton Mobility Index (DEMMI) assesses functionality in different positions (lying, sitting, standing, walking); absolute values range from zero to 19 points; higher scores reflect better functionality
Change in functionality (DEMMI total score, scaled values)
The de Morton Mobility Index (DEMMI) assesses functionality in different positions (lying, sitting, standing, walking); scaled scores range from zero to 100 points; higher scores reflect better functionality
Change in fear of falling
Subjective fear of falling assessed by self-report using the "Falls Efficacy Scale-International Version (FES-I)" questionnaire; results range from 16 to 64 Points; higher scores reflect greater fear of falling; total number of points will be analysed
Change in subjective intensity of the Lyra training
Subjective intensity assessed by self-report using the "Borg Rating of Perceived Exertion Scale" questionnaire; score range from 6 (no exertion at all) to12 (maximal exertion); higher scores represent greater subjective intensity and exertion of the Intervention training
Change in the THERA-Trainer Lyra machine settings
Settings of the THERA-Trainer Lyra gait training machine
Full Information
NCT ID
NCT03558841
First Posted
May 16, 2018
Last Updated
June 5, 2018
Sponsor
University Department of Geriatric Medicine FELIX PLATTER
Collaborators
University of Basel
1. Study Identification
Unique Protocol Identification Number
NCT03558841
Brief Title
Effect of Lyra Gait Training on the Mobility of Geriatric Rehabilitation Inpatients
Official Title
Effect of THERA-Trainer Lyra Gait Training in Addition to Physical Therapy on the Mobility of Geriatric Rehabilitation Inpatients Compared to Physical Therapy Alone: Randomized, Active-controlled, Parallel Group, Intervention Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Terminated
Why Stopped
enrollment goal not met in allotted recruitment period
Study Start Date
October 5, 2017 (Actual)
Primary Completion Date
March 29, 2018 (Actual)
Study Completion Date
March 29, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Department of Geriatric Medicine FELIX PLATTER
Collaborators
University of Basel
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
This study evaluates the effect of the addition of gait training to physical therapy on the gait of geriatric rehabilitation inpatients. Half of the patients will receive gait training with a gait training machine and conventional physical therapy in combination, the other half of the patients will receive conventional physical therapy alone.
Detailed Description
The geriatric rehabilitation inpatients recruited for this study primarily have difficulties with muscle weakness and walking generally due to a prolonged period of bed rest (as opposed to patients who primarily have cognitive disorders or neurological diseases), generalized muscle weakness and deconditioning. The rehabilitation goal for these patients is to be discharged home (not institutionalized) with improved mobility. Geriatric patients require intensive training in order to reach their pre-hospital levels of mobility and physical functional performance. Usual care involves physical therapy sessions, generally six times per week. Regaining mobility is crucial for quality of life and functional independence.
The aim of this intervention trial is to compare the effectiveness of Lyra gait training plus conventional physical therapy (intervention group) on gait compared to conventional physical therapy alone (control group) in geriatric rehabilitation patients. We hypothesize that, post-intervention, the intervention group will have better mobility and physical functional performance than the control group. Trial results will provide physical therapists and rehabilitation physicians with valuable information to better treat their inpatients and more efficiently use the limited time available for inpatient physical therapy sessions. Specifically, physical therapists should be better able to determine if the benefit of the Lyra gait trainer for geriatric rehabilitation inpatients with primarily muscle deconditioning is strong enough to warrant their extra time investment of providing the Lyra gait training. Results should also help determine in the future if the target population should continue with outpatient therapy after their discharge home. If this trial supports our hypothesis, then the trial results will provide data needed for the sample size calculation for a subsequent, larger trial.
The THERA-Trainer Lyra (from Ability AG, distributed by medica Medizintechnik GmbH) is an automated gait trainer with adjustable body weight support (no exoskeleton) and adjustable pedals (not a treadmill) that move in a physiological gait pattern derived from natural human walking movements. The upright position and the repetitive movement patterns activate muscle memory and allow safe gait training at the individual's performance limit throughout rehabilitation. The Lyra gait training is used to regain walking ability, improve gait speed, improve endurance and improve the gait pattern in geriatric rehabilitation patients.
Ten patients should be enrolled in this study:
Intervention group (n=5): Lyra gait training thrice weekly and conventional physical therapy (6 times per week) during inpatient period. After discharge home, continuation of thrice weekly Lyra gait training and discontinuation of physiotherapy.
Control group (n=5): Conventional physical therapy (6 times per week) during inpatient period. After discharge home, discontinuation of physical therapy.
At enrollment (Visit 1), all participants will be rehabilitation inpatients. The duration of the inpatient period will be determined clinically based on medical need and will thus vary from patient to patient. The average length of stay for the targeted population is approximately two weeks. Visit 2 will be performed shortly before the patient is discharged home. For each participant, the outpatient period (between Visit 2 and Visit 3) will be the same duration as the inpatient period (between Visit 1 and Visit 2).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mobility Limitation, Muscle Weakness
Keywords
gait, mobility, geriatric, rehabilitation, inpatient
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized, active-controlled
Masking
None (Open Label)
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Gait training with the THERA-Trainer Lyra (3x/week) in addition to conventional geriatric rehabilitation physical therapy (6x/week) during inpatient period. After discharge home, continuation of Lyra gait training (3x/week), discontinuation of physical therapy.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
Conventional geriatric rehabilitation physical therapy (6x/week) during inpatient period. After discharge home, discontinuation of physical therapy.
Intervention Type
Other
Intervention Name(s)
Gait training with the THERA-Trainer Lyra
Intervention Description
Gait training with the THERA-Trainer Lyra end-effector gait trainer 3x/week during the inpatient and the outpatient periods.
Intervention Type
Other
Intervention Name(s)
Physical therapy
Intervention Description
Conventional geriatric rehabilitation physical therapy (6x/week) during the inpatient period. After discharge home, discontinuation of physical therapy.
Primary Outcome Measure Information:
Title
Change in gait velocity
Description
Habitual, preferred ("normal") walking speed (cm/s) quantified with the GAITRite electronic walkway system
Time Frame
Baseline, after 2 weeks, after 4 weeks
Secondary Outcome Measure Information:
Title
Change in grip strength
Description
Grip strength (kg) of each hand (best result of two attempts for each hand used for data analysis)
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in general mobility
Description
Timed Up and Go Test time (seconds); faster test times represent better general mobility
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in spatial-temporal gait parameters (other than walking velocity)
Description
Gait parameters quantified with the GAITRite electronic walkway system
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in endurance
Description
Six Minute Walk Test; distance walked (meters) in six minutes; greater distance walked represents better endurance
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in functionality (DEMMI total score, absolute values)
Description
The de Morton Mobility Index (DEMMI) assesses functionality in different positions (lying, sitting, standing, walking); absolute values range from zero to 19 points; higher scores reflect better functionality
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in functionality (DEMMI total score, scaled values)
Description
The de Morton Mobility Index (DEMMI) assesses functionality in different positions (lying, sitting, standing, walking); scaled scores range from zero to 100 points; higher scores reflect better functionality
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in fear of falling
Description
Subjective fear of falling assessed by self-report using the "Falls Efficacy Scale-International Version (FES-I)" questionnaire; results range from 16 to 64 Points; higher scores reflect greater fear of falling; total number of points will be analysed
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in subjective intensity of the Lyra training
Description
Subjective intensity assessed by self-report using the "Borg Rating of Perceived Exertion Scale" questionnaire; score range from 6 (no exertion at all) to12 (maximal exertion); higher scores represent greater subjective intensity and exertion of the Intervention training
Time Frame
Baseline, after 2 weeks, after 4 weeks
Title
Change in the THERA-Trainer Lyra machine settings
Description
Settings of the THERA-Trainer Lyra gait training machine
Time Frame
Baseline, after 2 weeks, after 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
65 years of age or older
Rehabilitation inpatients at Felix Platter Hospital with primarily muscle weakness and difficulty walking
Community-dwellers before hospital admission with planned discharge home
Body weight 150 kg or less
Body height between 100 cm and 195 cm
Mini-Mental State Examination score 21 points or more
Signed informed consent for study participation
Exclusion Criteria:
Clinically significant neurologic or musculoskeletal diseases which severly affect walking, e.g. advanced Parkinson's disease or hemiplegia
Severe cardiac insufficiency
Advanced chronic pulmonary disease (COPD Gold IV)
Amputations of extremities (except missing fingers)
Blindness
Inability to understand and speak German well enough to understand the patient information, training and assessment instructions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephanie A. Bridenbaugh, M.D
Organizational Affiliation
Head of the Basel Mobility Center of the Felix Platter Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Felix Platter Hospital
City
Basel
ZIP/Postal Code
4002
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Effect of Lyra Gait Training on the Mobility of Geriatric Rehabilitation Inpatients
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