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Completed

NCT Number: NCT03330912

The Influence of Seat Height on Hemiplegic-pattern Propulsion of Manual Wheelchairs

This study evaluates the effect of seat height on hemiplegic-pattern wheelchair propulsion. Each subject will act as their own control and measures will be obtained in a one sixty minute session. Five seat heights relative to the subject's leg length will be measured in a random order to see the effect on forward and backwards wheelchair propulsion.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nova Scotia Rehabilitation and Arthritis Centre

Halifax, Nova Scotia, B3H 4K4, Canada

About this study

Many people who have suffered a stroke require a wheelchair for mobility. Hemiplegia is a common result of stroke.Many people with hemiplegia propel themselves using their sound-side arms and legs ("hemiplegic-pattern propulsion") in manual wheelchairs.Often people using this pattern are prescribed wheelchairs with a reduced seat height to facilitate foot propulsion. Despite the seeming obviousness of the need to lower the seat height for people who use foot propulsion,there is little available evidence to help establish optimal wheelchair seat height. The study objective is to test the hypothesis that there is an optimum wheelchair seat height (expressed as a percentage of the lower leg length) for hemiplegic-pattern wheelchair propulsion. The investigators expect that the optimum seat height will be lower than that usually used for wheelchairs that are hand-propelled.

A single-subject design with able-bodied participants will be used to investigate 5 randomized seat heights. The 5 seat heights will be set relative to the subjects leg length at a single 60 minute data collection session All measures will be obtained during one session. The optimal seat height will be chosen based on wheelchair propulsion speed, push frequency and effectiveness over 10m going forward on smooth surface, and 5m going backwards over a soft surface.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • willing to participate
  • is right-hand dominant (to simplify wheelchair and laboratory set-up)
  • has a subjective unshod height of ≤ 183 cm (6'0")
  • is able to be comfortably seated in the manual wheelchair used for the study
  • is 18 years of age or older, is alert and cooperative
  • is competent to provide informed consent
  • is able to communicate in English
  • does not have an unstable medical condition

Exclusion criteria

-

Treatment and study plan

Neutral seat height

Device

Seat height set relative to participant's leg length with neutral set at the measured lower leg length

Very low seat height

Device

Seat height set relative to participant's leg length, 2" below the measured lower leg length

Low seat height

Device

Seat height set relative to participant's leg length, 1" below the measured lower leg length

Very high seat height

Device

Seat height set relative to participant's leg length, 2" above the measured lower leg length

High seat height

Device

Seat height set relative to participant's leg length, 1" above the measured lower leg length

Primary outcomes

  1. speed (m/s)

    Time frame: same day measure obtained immediately after seat adjustment, approximately 10 minutes

    wheelchair propulsion speed over 10 m forward and 5 m backward

  2. push frequency (cycles per second)

    Time frame: same day measure obtained immediately after seat adjustment, approximately 10 minutes

    number of foot cycles completed over the 10 m forward and 5 m backward

  3. Propulsion effectiveness

    Time frame: same day measure obtained immediately after seat adjustment, approximately 10 minutes

    distance travelled per foot propulsion cycle

Secondary outcomes

  1. forward propulsion wheelchair skills test score

    Time frame: same day measure obtained immediately after seat adjustment, approximately 10 minutes

    fail, pass with difficulty or pass for wheeling forward 10 m

  2. propulsion difficulty questionnaire

    Time frame: same day measure obtained immediately after seat adjustment, approximately 10 minutes

    Investigator developed questionnaire asking how difficult it was to perform the propulsion test. The participant will self-report his/her level of difficulty for this skill using a five-point Likert scale (1 =very easy, 2=somewhat easy, 3=neither easy nor difficult, 4= somewhat difficult and 5=very difficult). A single number will be reported.

Sponsors and collaborators

Lead sponsor

Lee Kirby

Other

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Nov 6, 2017
Registry last updated
Sep 11, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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