Status:

ACTIVE_NOT_RECRUITING

Pilot Study of a Sedentary Behaviour Intervention for Individuals With a Spinal Cord Injury

Lead Sponsor:

Brunel University

Collaborating Sponsors:

Royal National Orthopaedic Hospital NHS Trust

Conditions:

Spinal Cord Injury

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Individuals with spinal cord injury have a greater risk of heart disease and stroke than non-disabled individuals. This might be partly because wheelchair users engage in high amounts of sedentary beh...

Detailed Description

Background: Individuals with a spinal cord injury are at a greater risk of heart disease and stroke than the general population. Many individuals with spinal cord injury sit for long periods due to b...

Eligibility Criteria

Inclusion

  • Individuals with self-reported paraplegia i.e. complete or incomplete SCI at T1 or below. Traumatic, non-traumatic, complete and incomplete SCI will all be eligible.
  • At least 18 years of age.
  • Self-report using a manual wheelchair as their primary mode of mobility inside and outside of the home.
  • Able to travel to Brunel University of London to undertake study measurements.
  • Access to use of a smartphone or tablet with internet access.
  • Able to communicate in English at a level sufficient to understand the study, complete study measurements and engage fully with the intervention.
  • Able to provide informed consent.
  • Willing and able to provide fingertip blood samples and fast prior to measurement sessions.
  • Able to independently transfer to a treatment couch and lay supine to undertake anthropometric measurements.

Exclusion

  • Self-reported heart condition, chest pain, dizziness, bone or joint problem, or any other condition that may be exacerbated by doing physical activity, as indicated via responses to the PAR-Q+.
  • Self-reported history of uncontrolled autonomic dysreflexia in the past 12 months.
  • Self-reported pregnancy.
  • Currently participating in another research project that involves an intervention.

Key Trial Info

Start Date :

May 12 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2025

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT06957483

Start Date

May 12 2025

End Date

December 31 2025

Last Update

September 22 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Brunel University of London

Uxbridge, London, United Kingdom, UB8 3PH