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Effect of Upper-body Rowing on Cardiometabolic Risk in Spinal Cord Injured Wheelchair Users

A

Aalborg University

Status

Completed

Conditions

Exercise Training
Spinal Cord Injuries

Treatments

Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT04390087
N-20190053

Details and patient eligibility

About

This randomized controlled trial will determine the effects of 12-weeks of wheelchair user-modified upper-body rowing on both traditional cardiometabolic risk factors in SCI manual wheelchair users.

Full description

This randomized controlled trial aims to determine the effects of 12-weeks of wheelchair user-modified upper-body rowing on both traditional (insulin resistance, obesity, dyslipidemia (including low HDL-C and elevated TG and blood pressure) and novel (inflammatory status, autonomic nervous system function, vascular structure and function, and cardiorespiratory fitness level) cardiometabolic risk factors in SCI manual wheelchair users. As secondary objectives, this trial will investigate the effects of the exercise intervention on free-living physical activity, shoulder pain, and indices of quality of life.

Men and women, aged 18-65 years; chronic SCI (≥1 year since injury); individuals with sufficient sparing of arm function to participate in upper-body rowing; using a manual wheelchair as a primary tool for mobility will be included in the trial.

The exercise training will be conducted as wheelchair-modified upper-body ergometer rowing. The training will be performed for up to 30 min, 3 times per week with moderate-to-vigorous intensity, with at least one rest day between sessions.

Outcome measurements will be performed immediately before (baseline), after (post) 12 weeks of training, and 6 months after the termination of the intervention period (follow up). This approach allows for assessment of the short term effects of exercise training as well as any residual effects from the training intervention on cardiometabolic risk, shoulder pain, indices of quality of life, and free-living physical activity

Enrollment

18 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-65 years;
  • chronic SCI (≥1 year since injury)
  • individuals with sufficient sparing of arm function to participate in upper-body rowing (i.e. as a minimum excluding individuals with complete SCI at or above C5)
  • using a manual wheelchair as a primary tool for mobility.

Exclusion criteria

  • Individuals who regularly engage in >150 min/week of moderate-to-vigorous intensity physical activity
  • have received a cortisone injection in the shoulder within the last four months
  • have had shoulder injury within the previous year
  • known medical issues (urinary tract infections, cardiovascular contraindications for exercise testing, and pressure sores)
  • diagnosed diabetes or any endocrine, heart, kidney, liver disease or any other disease that may limit the ability to perform exercise.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 2 patient groups

Exercise
Experimental group
Description:
Upper-body rowing performed up to 30 min, 3 times per week with moderate-to-vigorous intensity
Treatment:
Other: Exercise
Control
No Intervention group
Description:
The participants allocated to the control group will be asked to maintain their normal lifestyle throughout the intervention period

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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