Improving Propulsion of the Paretic Leg In Chronic Stroke

NCT ID: NCT04650802

Last Updated: 2020-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-03-04

Study Completion Date

2020-03-11

Brief Summary

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Stroke survivors may have a latent, propulsive capacity of the paretic leg, that can be elicited during short, intensive gait training interventions. The aim of this study was therefor to investigate the effect of a five-week gait training on paretic propulsion, propulsion symmetry, gait capacity, and daily-life mobility and physical activity in chronic stroke survivors.

Detailed Description

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Stroke survivors may have a latent, propulsive capacity of the paretic leg, that can be elicited during short, intensive gait training interventions. The aim of this study was therefor to investigate the effect of a five-week gait training on paretic propulsion, propulsion symmetry, gait capacity, and daily-life mobility and physical activity in chronic stroke survivors. We hypothesize that the robotic gait training will improve propulsion symmetry and, thereby, gait speed and functional gait tasks. In addition, we expect that improved gait capacity might lead to less impact of stroke on daily-life mobility and a higher physical activity level. Thirty-three chronic stroke survivors with impaired paretic propulsion (≥8% difference in paretic vs. non-paretic propulsive impulse) will be enrolled in this proof-of-concept study. Participants receive five weeks individual robotic gait training targeting paretic propulsion (60 minutes, two time a week). The robotic gait training is complemented with daily home exercises (15 minutes/day) focusing on increasing strength and practice of learned strategies in daily life. Propulsion measures, self-selected gait speed, performance on functional gait tasks, and daily-life mobility and physical activity are assessed five weeks (T0) and one week (T1) before the start of the intervention, and one week (T2) and five weeks (T3) after the end of the intervention.

Conditions

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Stroke

Keywords

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Gait Rehabilitation Robotics Propulsion Speed Biomechanics

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Longitudinal intervention study with two consecutive baseline assessments and a five-week follow-up
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Gait training

Participants receive five weeks individual robotic gait training in LOPES II, targeting paretic propulsion (60 minutes, two time a week). The robotic gait training is complemented with daily home exercises (15 minutes/day) focusing on increasing strength and practice of learned strategies in daily life.

Group Type EXPERIMENTAL

Gait training

Intervention Type DEVICE

Participants receive five weeks individual robotic gait training in LOPES II, targeting paretic propulsion (60 minutes, two time a week). The robotic gait training is complemented with daily home exercises (15 minutes/day) focusing on increasing strength and practice of learned strategies in daily life.

Interventions

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Gait training

Participants receive five weeks individual robotic gait training in LOPES II, targeting paretic propulsion (60 minutes, two time a week). The robotic gait training is complemented with daily home exercises (15 minutes/day) focusing on increasing strength and practice of learned strategies in daily life.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* adults (\>18 years of age) with unilateral ischemic or heamorrhagic supratentorial stroke
* at least 6 months post-onset
* impaired propulsion of the paretic leg during walking at a self-selected speed (≥ 8 percent propulsion asymmetry)
* ability to walk 10 meter without support or use of a walking aid (Functional Ambulatory Categories (FAC) 3-5)
* ability to walk for 5 consecutive minutes, with or without the use of a walking aid
* at least 10 degrees passive hip extension and able to stand plantigrade with extended knee

Exclusion Criteria

* inability to move the body upward against gravity (calf muscle - Medical Research Council (MRC) scale \< 3)
* severe cognitive problems assessed with Mini-Mental State Examination (MMSE \< 24)
* depressed mood assessed with the Hospital Anxiety and Depression Score (HADS \> 7)
* persistent unilateral visuospatial neglect assessed with the Star Cancellation Test (score \< 44)
* any medical condition interfering with gait
* inability to understand verbal instructions
* inappropriate or unsafe fitting of the robotic gait trainer, due to severe lower limb spasticity (Modified Ashworth Scale (MAS) ≥ 3), severe lower limb contractures, body weight ≥ 140 kg, or skin problems at body sites where the harness or straps were to be fitted
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Radboud University Medical Center

OTHER

Sponsor Role collaborator

Sint Maartenskliniek

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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ACH Geurts, Prof. dr.

Role: PRINCIPAL_INVESTIGATOR

Radboud University Medical Center

Locations

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Sint Maartenskliniek

Ubbergen, Gelderland, Netherlands

Site Status

Countries

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Netherlands

References

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Alingh JF, Groen BE, Kamphuis JF, Geurts ACH, Weerdesteyn V. Task-specific training for improving propulsion symmetry and gait speed in people in the chronic phase after stroke: a proof-of-concept study. J Neuroeng Rehabil. 2021 Apr 23;18(1):69. doi: 10.1186/s12984-021-00858-8.

Reference Type DERIVED
PMID: 33892754 (View on PubMed)

Other Identifiers

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R201605453

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

785_LOPES I-PICS

Identifier Type: -

Identifier Source: org_study_id