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Backward Walking Observation Training in People With Stroke and Gait Quality in Stroke

N

National Yang Ming Chiao Tung University

Status

Enrolling

Conditions

Stroke

Treatments

Other: Non-motor observational backward walking training
Other: Backward walking observation training

Study type

Interventional

Funder types

Other

Identifiers

NCT06850662
NYCU113210AF2

Details and patient eligibility

About

Walking impairment is one of the most common and concerning issues for individuals with stroke. Previous studies have often used improvements in walking speed and distance as reference indicators for gait performance progress in individuals with stroke. However, for people with chronic stroke, it may be more appropriate to prioritize improving gait symmetry and gait variability to enhance gait quality as a primary intervention goal. Additionally, stroke can lead to an imbalance in interhemispheric brain activity, which evolves as motor function recovers. According to the literature review, backward walking may extend the support time of the lower limbs, thereby enhancing the weight-bearing capacity of the affected limb. This, in turn, could promote gait symmetry and reduce gait variability. Changes in brain activity might also accompany such improvements in gait quality. Therefore, this study aims to investigate the immediate, short-term and post carryover intervention effects of backward walking observation training on gait quality in individuals with chronic stroke as well as to explore its effects on interhemispheric activity balance in individuals with chronic stroke.

Enrollment

50 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥ 6 months after the diagnosis of stroke
  • Independent walking over at least 7m with or without a walking aid
  • Mini-mental state examination score ≥ 24

Exclusion criteria

  • Had difficulty in backward walking
  • Any neuromuscular disorders history
  • With visual or auditory disorders
  • Unstable cardiac status or uncontrolled hypertension
  • Any musculoskeletal disorders that would affect walking ability

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Backward walking observation training group
Experimental group
Description:
The intervention is a 50-minute session and 3 sessions/week, totaling 4 weeks.
Treatment:
Other: Backward walking observation training
Non-motor observational backward walking training group
Active Comparator group
Description:
The intervention is a 50-minute session and 3 sessions/week, totaling 4 weeks.
Treatment:
Other: Non-motor observational backward walking training

Trial contacts and locations

1

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Central trial contact

Yea-Ru Yang, PhD

Data sourced from clinicaltrials.gov

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