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NCT05989906Enrolling by invitation

Feasibility of a Sprint Interval Training Program During Inpatient Spinal Cord Injury Rehabilitation

Feasibility of a Sprint Interval Training Program During Inpatient Spinal Cord Injury Rehabilitation: A Pilot Randomized Controlled Trial
University of WashingtonClinicalTrials.govbehavioral
Study focus
Disease/Condition
Spinal Cord Injuries
Drug/Device/Intervention
Sprint Interval Training (SIT)
Study type
Interventional
Intervention type
behavioral
Sponsor & location
Primary sponsor
University of Washington
Location
Seattle, United States of America
Timeline & enrollment
Phase
N/A
Start date
Aug 23, 2023
End date
Aug 01, 2025
Enrollment
32 participants
Primary outcome

Total physical activity (vector magnitude) per week,Percentage of participants that complete at least six Sprint Interval Training (SIT) sessions,Total number of Ergometer (ERGO) sessions that participants complete between treatment completion and 6 month follow up,Percentage of participants that adhere to Sprint Interval Training sessions and received Motivational Interviewing (MI) sessions

Summary

This study will assess the feasibility and efficacy of 3 treatments to increase physical
 activity during and after inpatient rehabilitation (IPR) for new spinal cord injuries:
 
 1. Program of sprint interval training (SIT) on an arm crank ergometer during IPR
 
 2. SIT + Provision of an arm ergometer (ERGO) for home use
 
 3. SIT + ERGO for home use + Motivational interviewing to increase adherence to exercise
 during and after IPR.
 
 The primary outcome is minutes per week of moderate to vigorous physical activity at 6 months
 after IPR discharge. Secondary outcomes include peak power on the 6-Minute Arm Test at IPR
 discharge and self-reported physical activity, depression, fatigue, pain, community
 participation, and quality of life at 6 months after IPR discharge. The investigators will
 obtain data on feasibility, acceptability, and perceived benefits of the treatments from
 stakeholders. The results of this pilot study will inform the design of a larger randomized
 trial.

ICD-10 classifications
Sequelae of injury of spinal cordOther and unspecified injuries of thoracic spinal cordOther and unspecified injuries of cervical spinal cordOther injury of lumbar spinal cordInjury of spinal cord, level unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05989906
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05989906 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Washington and is currently Enrolling by invitation. The study focuses on Spinal Cord Injuries. Target enrollment is 32 participants.

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