Hybrid High-intensity Interval Training for Persons With Spinal Cord Injury. A Feasibility Study

Not Applicable

Completed

• Conditions: Spinal Cord Injuries
• Interventions: Other: hybrid high-intensity training

• Registration Number: NCT04211311
• Lead Sponsor: University of Southern Denmark

Brief Summary

This study examines safety and feasibility of a study protocol using a combination of functional electrical legcycling with voluntary armwork (hybrid training) as either skiergometer or armcycling in high intensity intervals for persons with spinal cord injury paraplegia.

Detailed Description

Cardiovascular disease is one of the most common causes of early death in people with spinal cord injury. Physical activity at high intensity is known to reduce the risk of cardiovascular disease in other patient groups.

During aerobic training, combining functional electrical stimulation (FES) with voluntary arm-work induces a higher oxygen uptake than FES cycling alone and high intensity interval training induces higher oxygen uptake than training at continuous intensity. The hypothesis is that combining hybrid training with high-intensity induces even higher oxygen uptake thereby reducing the risk of cardiovascular disease. This training modality has not been tested before, so before conducting a randomized controlled trial testing the effect of this training modality on oxygen uptake, the aim was to asses safety and feasibility of this protocol.

Study Timeline

• Study Start: 2018-01-30
• Primary Completion: 2018-04-26
• Study Completion: 2018-06-01
• Study First Submitted: 2019-10-10
• Status Verified: 2019-12
• Study First Submitted QC: 2019-12-20
• Last Update Submitted: 2019-12-20
• Study First Posted: 2019-12-26
• Last Update Posted: 2019-12-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 8

Inclusion Criteria

• spinal cord injury paraplegia,
• complete and incomplete lesions,
• ability to be electrically stimulated,
• willing to train 3 times a week at high intensity

Exclusion Criteria

• heart pacemaker or other heart problems contradicting high intensity aerobic training,
• pregnancy,
• unstable fractures,
• cancer,
• heterotopic ossification,
• myositis ossificans,
• severe osteoporosis,
• pressure ulcers,
• newly implanted metal,
• newly surgery,
• frequent episodes of autonomic hyperreflexia,
• very high or low blood pressure,
• dislocation or subluxation of joints
• high level of shoulder pain at study start.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
FES-legcycling with voluntary arm-work	hybrid high-intensity training	FES-legcycling combined with arm ski-ergometer or arm-cycling

Primary Outcome Measures

Name	Time	Method
Number of serious adverse events	8 weeks	Assessed by number of incidences of autonomic hyperreflexia or acute cardiac events
intensity	8 weeks	Assessed as mean intensity of the 4 x 4 min. intervals as proportion of peak watt measured at baseline test. Peakwatt for FES-cycling was defined as an average of the three highest watt values within 30 sec. For skiergometer peak watt was defined as the highest average of one min. splits.
Shoulder pain	8 weeks	Measured using Wheelchair Shoulder Pain Index (WUSPI), a 15 item questionnaire measuring shoulder pain during daily activities. Each item is scored on a 10 mm visual analog scale with anchors no pain to worst pain ever. Total index score range from 0 - 100. Within each item there is a not applicable option. The score used is performance corrected WUSPI score, dividing total index score by number of item responses and multiplied by 15. Higher score indicate higher level of shoulder pain.
compliance	8 weeks	Assessed with number of dropouts and proportion of fulfilled training minutes

Secondary Outcome Measures

Name	Time	Method
Peak oxygen uptake	8 weeks	Assessed measuring pulmonary gas exchange. Peak oxygen uptake is defined as respiratory exchange ratio of 1.05 or higher, concentration of blood lactate of 7 mmol/l or more and subjective rating of perceived exertion on the Borg 6-20 scale of min. 16.
leisure time physical activity	8 weeks	leisure time physical activity measured with leisure time physical activity questionnaire - SCI (LTPAQ-SCI), asking number of min. spent performing low-, moderate and high intensity leisure time physical activity pr. day, scored by multiplying number of min by number of days yielding number of minutes of leisure time physical activity per week.
health related quality of life	8 weeks	health related quality of life measured with Short Form 36 (SF-36), categorically based on a three to six categories Likert scale. An algorithm transforms the scores into a 0-100 scoring system, with higher scores indicating better quality of life
Fatigue	8 weeks	Assessed with the Multi Dimensional Fatigue Inventory (MFI-20) covering 5 dimensions of fatigue which are scored using a five level scale. Sub scale scores range 4-20 are calculated as the sum of item ratings and total fatigue score range 20-100 is calculated as the sum of sub scale scores with higher scores indicating lower level of fatigue.

Trial Locations

Locations (1)

Specialhospitalet for Polio og Ulykkesramte; 🇩🇰 Rødovre, Denmark