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Lateral Perturbation Induced Step Training Compared to Lateral Voluntary Step Training in People with Chronic Stroke

V

Vicki Gray

Status

Completed

Conditions

Stroke

Treatments

Other: Perturbation Induced Step training
Other: Voluntary step training

Study type

Interventional

Funder types

Other

Identifiers

NCT06638476
American Heart Association
00056550
P30AG028747 (U.S. NIH Grant/Contract)
H133P100014, H133F140027 (Other Grant/Funding Number)

Details and patient eligibility

About

The goal of this clinical trial is to see if perturbation-induced step training improves stepping performance during a reactive and voluntary step. The main questions it aims to answer are:

Does perturbation induced step training improve step initation time and first recovery step?

Researchers will compare lateral perturbation induced step training to lateral voluntary step training to see if the first recovery steps improve.

Participants will:

Vist the lab for an initial assessment, post exercise and one month post exercise of voluntary and perturbation induced stepping performance, and clinical tests of balance, motor recovery, sensory and strength tests.

Exercise 3 times a week for 6 weeks in person

Track falls for 6 months after the exercise.

Full description

Stroke is the leading cause of disability in the United States as the result of an increased survival rate over the last 25 years. A high frequency of falls is commonly reported in this group due to the residual sensorimotor deficits and impairments to balance. Many falls occur when weight is transferred laterally and an equal number of falls happen during voluntary movements as during unexpected disturbances such as a trip, push or pull. Typically, either will involve a protective step to recover balance. Thus, the purpose of this study is to compare the effects of reactive lateral step training to voluntary lateral step training on the performance of the protective step, functional balance and falls in persons post-stroke. Thirty participants with a stroke will be randomized to one of two interventions, reactive step training or voluntary step training. In the voluntary step training group, participants will perform voluntary steps. In the reactive step training group, participants will perform reactive steps generated by the Active Step. The training will be 3 times a week for 6 weeks. The step initiation time, will be compared in both the voluntary and reactive steps at baseline before the intervention, post-intervention and a test of retention will occur one month after the training. Functional balance will be assessed with the Community Balance & Mobility Scale and falls will be compared in the 6 months preceding the intervention to 6 months post-intervention testing. If reactive step training is effective, then the protective step characteristics, functional balance and the number of falls will be reduced compared to the voluntary step training group.

Enrollment

31 patients

Sex

All

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Hemiparesis as a result of a stroke greater than 6 months previous to the study
  • Able to walk 10 meters with or without a walking aid
  • Have the cognitive ability to give informed consent

Exclusion criteria

  • Medical condition precluding participation in regular exercise, such as acute cardiac or respiratory conditions limiting activity and other health conditions significantly impacting the ability to walk beyond the effects of the stroke, such as other neurological conditions or peripheral neuropathies.
  • Bilateral stroke or a previous stroke in the contralateral hemisphere.
  • Aphasia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

31 participants in 2 patient groups

Perturbation induced step training
Experimental group
Description:
Participants will receive 18 sessions over 6 weeks.
Treatment:
Other: Perturbation Induced Step training
Voluntary Step training
Active Comparator group
Description:
Participants will receive 18 sessions over 6 weeks.
Treatment:
Other: Voluntary step training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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