Optimization of Adaptive Rowing Seating

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVA Office of Research and Development

About this trial

Adaptive sports programs are integral components to combating Veteran isolation, promoting wellbeing and seeking to build teams, networks, communities. These activity-based communities are medicine free treatment systems enhancing Veterans' health from a holistic perspective. This approach to Veteran healthcare is critical as studies indicate Veterans not only have 56% higher perceived social isolation but are also 1.5x more susceptible to suicide than the general public. It is imperative to improve access to exercise and physical activity through adaptive sport or recreation. This proposal is going to focus on Adaptive Indoor Rowing for Veterans with limited or changing trunk stability (i.e. SCI/D, paralysis, paresis, etc.). Rowing is a unique full-body activity that increases cardiovascular demand and increases coordination and aerobic capacity through movement. This proposal aims to address critical gaps in adaptive rowing technology and provide Veterans with limited trunk stability access to full stroke adaptive rowing.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

central nervous system impairment

spinal cord injuries with single neurological level in the cervical to lumbosacral region

cerebrovascular accident with associated sequelae including but not limited to hemiparesis and spasticity

neurodegenerative disorders including but not limited to amyotrophic lateral sclerosis, multiple sclerosis, multiple system atrophy, and parkinsonism

Disqualifiers

acute illness or injury

active or recent pressure injuries in the last 6 months affecting their ability to safely row (e.g., the coccyx, ischial tuberosity, sacrum, etc.)

Individuals who would be classified as NE or PR3-PD - FISA Para-Rowing Classifications

Flap procedure to address pressure injury less than one year prior

Trial design

Design model

Crossover

Treatments tested in this trial

  • Adaptive Indoor Rowing Seat

    Device

    Light weight adjustable indoor rowing seat for Veterans with limited trunk stability.

  • Paddle Sport adaptive seating system

    Device

    On market comparator (discontinued) adaptive indoor rowing seat for individuals with limited trunk stability.

Treatment groups

15 Participants
are divided into 2 treatment groups
Group A: AIRS V2Experimental treatment 1 intervention
Group B: Paddle Sport Adaptive Seating SystemExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Trunk Movement

Changes in angular trunk position (degrees) will be captured during a self-selected, moderate pace for 2-5 minutes depending on their ability. They will complete 3 trials of rowing with at least 10 minutes of rest between trials on each seat.

Time frame
up to 4 weeks after enrollment
2

Rowing Stroke Length

Changes in stroke length (cm) will be captured during a self-selected, moderate pace for 2-5 minutes depending on their ability. They will complete 3 trials of rowing with at least 10 minutes of rest between trials on each seat.

Time frame
up to 4 weeks after enrollment
3

Power (Watts)

Changes in power generation (Watts) will be captured during a self-selected, moderate pace for 2-5 minutes depending on their ability. They will complete 3 trials of rowing with at least 10 minutes of rest between trials on each seat.

Time frame
up to 4 weeks after enrollment
4

Custom Usability Items

Questions study specific to the usability of the indoor rowing seats

Time frame
up to 4 weeks after enrollment

Secondary outcomes

Other outcomes

Sponsors and contacts

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VA Office of Research and Development

Lead sponsor

Louis Stokes VA Medical Center

Collaborator

This trial is not recruiting at the moment. You can still explore other options: