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Sprint Interval Training During Rehabilitation After Spinal Cord Injury

Sprint Interval Training During Rehabilitation After Spinal Cord Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03709095
Acronym
SprintSCI
Enrollment
20
Registered
2018-10-17
Start date
2017-06-01
Completion date
2018-06-01
Last updated
2018-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise, Rehabilitation, Spinal Cord Injuries

Keywords

Inpatient Rehabilitation, Sprint interval training, Exercise, Spinal Cord Injury

Brief summary

Immediately following a spinal cord injury (SCI), patients are admitted to inpatient rehabilitation where they undergo physical reconditioning in preparation for a return to home setting. The current standard of practice for aerobic training is performing arm-ergometry for 25 mins at a frequency of three times per week. Given the move towards shortened length of stay during inpatient rehabilitation, performing MICT can consume a considerable amount of therapy time. Sprint interval training (SIT) has been shown to elicit similar improvements in physical capacity, despite a reduced time commitment to MICT. However, there are no controlled trials comparing the effects of SIT to MICT in individuals with SCI undergoing inpatient rehabilitation. The primary aim of this study was to investigate the efficacy of a five-week, thrice weekly 10 min SIT program and compare outcome measures to a traditional 25 minute MICT program on the arm-ergometer in individuals with SCI undergoing inpatient clinical rehabilitation. It was hypothesized that five weeks of SIT and MICT would induce similar changes in maximal and sub-maximal exercise performance, self-efficacy for exercise, and exercise enjoyment, despite large differences in training volume and time commitment. It was also hypothesized that SIT would be well tolerated and elicit higher levels of cardiovascular strain than MICT.

Interventions

Participants utilized the arm ergometer for improving aerobic exercise capacity

OTHERmoderate intensity continuous training

Participants utilized the arm ergometer for improving aerobic exercise capacity

Sponsors

Hamilton Health Sciences Corporation
CollaboratorOTHER
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants were randomized to one of two groups: (A) sprint interval training (SIT) or (B) moderate intensity continuous training (MICT).

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants with sub-acute spinal cord injury (time since injury: 14 - 182 days) * Undergoing inpatient rehabilitation * Aged 18-65 years * Injury level at the second cervical vertebrae (C2) or below

Exclusion criteria

\- Unable to perform arm-ergometry training

Design outcomes

Primary

MeasureTime frameDescription
Change in peak power outputChange in peak power output from baseline to 5 weeksmaximum amount of power produced during a graded exercise test on the arm-ergometer
Change in sub-maximal arm-ergometryChange in sub-maximal arm-ergometry from baseline to 5 weeksParticipants performed three 5-minute steady state workloads on the arm-ergometer at power outputs corresponding to RPE's of 8, 10 and 12. Participants were given a minimum of 2 minutes, and a maximum of 5 minutes of rest in between each workload.

Secondary

MeasureTime frameDescription
Change in self-efficacy for exerciseChange in self-efficacy from baseline to 5 weeksUsing a self-reported questionnaire, participants rated how confident they are with regards to performing and carrying out regular physical activities and exercises.
Cardiovascular ResponsesThroughout each week of training (Week 1,Week 2, Week 3, Week4, Week 5)Monitored heart rate throughout each training session
Pain perceptionsMeasured only at the end of the intervention (5 weeks)Through a questionnaire, participants rated how much shoulder pain, bodily pain, and physical discomfort they typically experience throughout the day and how much pain they experienced with the intervention they were allocated to.
Exercise SatisfactionMeasured only at the end of the intervention (5 weeks)Participants completed the Physical Activity Enjoyment Scale (PACES) in order to asses the level of enjoyment with the training intervention they received.
Perceptual ResponsesThroughout each week of training (Week 1,Week 2, Week 3, Week4, Week 5)Monitored ratings of perceived exertion throughout each training session

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026