Effect of Antigravity Treadmill Training on Cardiorespiratory Fitness and Lower Limb Function in Incomplete Spinal Cord Injury

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorMiddle East University

About this trial

This study aims to investigate the effect of locomotor training using an antigravity treadmill on cardiorespiratory fitness and lower limb function in patients with incomplete spinal cord injury.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Injury duration more than 3 months

Ability to stand with or without assistance

Medically stable condition

Disqualifiers

Complete spinal cord injury

Severe cardiopulmonary disorders

Severe osteoporosis or fractures

Severe cognitive impairment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Antigravity Treadmill for gait training

    Device

    Antigravity treadmill for gait training

  • gait training and balance exercise

    Other intervention

    gait training between Parallel bar Balance Exercise

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Study GroupActive comparator 2 interventions
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Cardiorespiratory fitness

Cardiopulmonary fitness will be measured by Cardiopulmonary Exercise Testing (CPET) to assess the integrated function of the cardiovascular, pulmonary, and muscular systems during exercise. The gold-standard parameter obtained from CPET is: VO₂max VO₂max: Maximum rate of oxygen consumption achieved during maximal exercise. Units: mL/kg/min

Time frame
At base line and 12 weeks
2

Lower Limb Function

Lower limb function will be measured by 10-Meter Walk Test (10MWT) is a simple and reliable measure of walking speed, Assesses: Gait speed Procedure Mark a 10-meter walkway. The patient will walks at: Comfortable/self-selected speed (usual gait speed) Walking Speed (m/s)= Distance (m) /Time (s)

Time frame
At base line and 12 weeks

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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