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Functional Interval Training for People With Spinal Cord Injury and Their Care Partners (SCI-FIT)

A

Arkansas Colleges of Health Education

Status

Completed

Conditions

Spinal Cord Injuries

Treatments

Behavioral: High Intensity Interval Exercise Training Group

Study type

Interventional

Funder types

Other

Identifiers

NCT05221723
PT-2021-024

Details and patient eligibility

About

Functional Interval Training for People with Spinal Cord Injury and Their Care Partners (SCI-FIT) aims to address barriers to physical activity for people with spinal cord injury and their care partners. This research study provides free, twice weekly group-based, adaptable exercise classes for people with spinal cord injury and their care partners.

Full description

Regular physical activity, and more specifically exercise, is beneficial for people with and without spinal cord injury (SCI). Unfortunately, people with spinal cord injury (pSCI) are less physically active than adults without SCI and are at an increased risk of cardiovascular disease. Care partners, or those who provide frequent assistance to those living with SCI, also achieve low physical activity levels and share similar health risks as a result. Often there are limited opportunities for pSCI to engage in regular exercise. In addition, pSCI and their care partners often face significant barriers to exercise including 1) lack of exercise participation opportunities; 2) cost of quality exercise instruction; 3) inaccessible exercise equipment or environments; 4) lack of social support from family and peers. This study, Functional Interval Training for People with Spinal Cord Injury and Their Care Partners (SCI-FIT) will explicitly address the barriers to exercise pSCI and their care partners often face with the primary goals of improving the health, physical activity levels, and quality of life of pSCI and their care partners. In order to address these goals, SCI-FIT will provide no-cost, twice weekly, group-based, adaptable exercise programming for pSCI and their care partners. All participants will be required to have physician or advanced practice provider clearance to exercise and will be evaluated by a physical therapist at no-cost prior to beginning the intervention to assess eligibility for the study. All eligible participants will complete a demographics questionnaire and will undergo a battery of baseline outcome assessments prior to undergoing the exercise intervention. Participants will complete 6-months of twice weekly group exercise classes aimed and hypothesized to increase physical activity levels, muscular strength, social support for exercise, functional mobility, peak power output, aerobic capacity, and quality of life for people with spinal cord injury and their care partners. Participants will repeat baseline outcome assessments at study midpoint (3-months) and study completion (6-months).

Enrollment

23 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Spinal Cord Injury: Must have a clinical diagnosis of spinal cord injury at level C5 (ASIA A-D) and/or must possess at least 4/5 elbow flexion muscular strength
  • Care Partners: self-identified care partner of a person with spinal cord injury participating in the study
  • Must be at least 18 years of age
  • Must be able to communicate and read in English
  • Must have physician or advanced practice provider clearance to exercise
  • Must provide their own transportation to and from the research study
  • Must be able to ambulate independently and/or propel a power or manual wheelchair independently
  • Care Partners: self-identified care partner of a person with spinal cord injury participating in the study

Exclusion criteria

  • Less than 4/5 elbow flexion muscular strength
  • Unable to ambulate independently or propel a power or manual wheelchair independently
  • Unable to provide transportation to and from the research study
  • Unable to communicate in English
  • Unable to present documented medical clearance to exercise from physician or advanced practice provider

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

23 participants in 1 patient group

Exercise Group
Experimental group
Description:
In this single group design, all participants will be provided with 6 months of twice weekly supervised group exercise.
Treatment:
Behavioral: High Intensity Interval Exercise Training Group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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