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Effects of Walking Training on Different Surfaces on Walking Ability in Ambulatory Patients With Spinal Cord Injury

Effects of Walking Training on Different Surfaces on Walking Ability, Balance Control, Lower Limb Muscle Strength, and Falls in Ambulatory Patients With Spinal Cord Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03622710
Enrollment
72
Registered
2018-08-09
Start date
2017-07-01
Completion date
2019-01-16
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rehabilitation, Spinal Cord Injuries

Keywords

Rehabilitation, Surfaces, Walking, Spinal cord injury

Brief summary

The study compares effects of 4-week walking training program on a walking track with difference surface \[WTDS\] and a firm ground on functional ability of ambulatory individuals with incomplete spinal cord injury \[iSCI\], using within- and between-group comparisons.

Interventions

OTHERRehabilitation therapy

Subjects are trained to walk overground (control) or over WTDS (experimental) for 5 days/week over 4 week. Then they will be monthly follow-up for fall data.

Sponsors

Khon Kaen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age at least 18 years 2. Having an incomplete SCI (the American Spinal Cord Injury Association (ASIA) Impairment Scale or AIS C or D) (Kirshblum et al., 2011) 3. At a sub-acute or chronic stage of injury (post injury time: PIT \> 3 months) (Wirth et al., 2008; Blackwell et al., 2001) 4. Able to walk with or without a walking device for at least 10m (Behrman et al., 2005; Lam et al., 2008; Jackson et al., 2008) 5. Having a body mass index (BMI) between 18.5-29.9 kg/m2 (Woo et al., 2007)

Exclusion criteria

1. Having an SCI from a progressive disease such as multiple sclerosis or malignancy 2. Having other medical conditions that might affect ambulatory ability, such as pain in the musculoskeletal system with an intensity of pain more than 5 out of 10 on a numeric rating pain scale (Dijkers, 2010), deformities of the spine and lower extremities (i.e. scoliosis, kyphosis, and equinovarus) and other neurological or other medical disorders (thromboembolism, autonomic dysreflexia). 3. Severe spasticity of the lower extremities (Modified Ashworth Scale (MAS) more than 2) (Bohannon & Smith, 1987; Scivoletto et al., 2008).

Design outcomes

Primary

MeasureTime frameDescription
10-meter walk test (10MWT)Change over 4 weeksSubjects walk at a comfortable pace along a 10m walkway. The test records the time use over the middle 4m of the walkway in order to minimize acceleration and deceleration effects. Then the average time over the 3 trials is converted to walking speed using the formula v=distance (m) /time (s)

Secondary

MeasureTime frameDescription
Timed up and go test (TUGT)Change over 4 weeksSubjects stand up from a standard armchair, walk around a traffic cone that is located 3m away from the chair, and return to sit down on the chair at a maximum and safe speed. The test records the time taken from the command Go until the subject's back against the backrest of the chair. Then the average times finding over the 3 trials is used for data analysis.
Five times sit-to-stand test (FTSST)Change over 4 weeksThe time taken to complete 5 chair-rise cycles at a fastest and safe speed is measured for each subject. Then the average time over the 3 trials is used for data analysis.
6-minute walk test (6MWT)Change over 4 weeksSubjects walk along a rectangular walkway as long as possible in 6 minutes. Every minute during the test, they are informed the time left and encouraged to continue in a good manner. Subjects are able to take a period of rest as needed and continued walking as soon as they can. The distance covered after 6 minutes are recorded
Incidence of fallSix months after completing the training program.Then subject will be monthly monitored for the fall data during 6 months using a fall diary and telephone.

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026