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Physical Fitness, Exercise Self-efficacy, Physical Activity Level in People With Spinal Cord Injury (SCI)

The Effects of Graded Exercise Integrated Education on Physical Fitness, Exercise Self-efficacy, and Physical Activity Level in People With Spinal Cord Injury

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03420170
Enrollment
40
Registered
2018-02-05
Start date
2018-04-30
Completion date
2019-04-30
Last updated
2018-02-05

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

Conditions

Physical Disability, Spinal Cord Injuries

Keywords

Spinal Cord Injuries, Physical Fitness, Exercise Self-Efficacy, Physical Activity

Brief summary

This is a single blind randomized controlled trial study which will conducted on people with paraplegia wheelchair users. The objectives of this study is to investigates the effects of 16 weeks of 'Graded Exercise Integrated Education' over conventional physical therapy on physical fitness, exercise self-efficacy and the level of physical activity. There will be a significant difference between the experimental and control group.

Detailed description

A study protocol will be a single blinded randomised controlled trial. 40 subjects with diagnosed of paraplegia (T1 and below) and dependent with wheelchair will be randomly assigned into 2 groups, Graded exercise (n=20) or Conventional Physical Therapy (n=20). In 8 weeks, the graded exercise group will receive strengthening and aerobic exercise for 2 times a week, and the controlled group will continue their normal routine. The strengthening exercise will consist of strength training for major upper limb muscles in the multigym station and free weights dumbbell whereas the aerobic exercise will perform by using arm ergometry, boxing and wheelchair wheeling. The exercise will be graded and progressed for each week in 8 weeks. The graded exercise group also will receive educational intervention to increase the exercise self-efficacy and physical activity level which will conduct in face to face for 2 times a week in 8 weeks during in-rehabilitation program and once on every 4 weeks in 8 weeks after discharge from in-rehabilitation program. The outcomes are the strength and endurance of upper limb which will be measure by using a BIODEX® Isokinetic Machine and hand grip strength by JAMAR® Hand-held dynamometry. The cardiovascular endurance will be measure by using 6 minute wheelchair push test (6MWPT). The exercise self-efficacy and physical activity level will be measure by using 'Exercise Self-Efficacy Scale (ESES)' and 'Physical Activity Scale for Individual with Disability (PASIPD)'. The outcome measure will be evaluated at the baseline level, week 4th, week 8th, week 12th, and 16th. Statistical analysis will be carried out using the SPSS 21.0 program for Windows and a significant level of p ≤ 0.05 will be used for all tests.

Interventions

OTHERGraded Exercise Integrated Education

Aerobic exercise Wheelchair propelling, boxing, hand cycling (2 rounds) 1. 3 mins. exercise and 2 mins. rest 2. Increased to 4.5 mins. and 30 sec. rest Strengthening exercise: Vertical chest press, butterfly press; vertical row and wide lattissimus pull down 3 sets, 10 reps. and 2 min rest between sets, moderate to vigorous intensity (50% of 1 RM) Educational intervention: The educational intervention for exercise self-efficacy and physical activity level (2 hours a week for 8 weeks during in rehabilitation and once a month for 8 weeks after discharge from rehabilitation)

OTHERConventional Physical Therapy

Normal routine of physical therapy including mobility training, wheelchair skills, resistance exercise, aerobic training, balance exercise, functional exercise

Sponsors

Universiti Teknologi Mara
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Traumatic and Non-traumatic paraplegia * Wheelchair dependent * Age range between 18 and 65 years old

Exclusion criteria

* Pregnancy * Individual who suffered from progressive neurological diseases, depression and mental disorder * Individual with frequent autonomic dysreflexia and hypotension * Individual with comorbid recent fracture * Individual with severe heart diseases and pain * Individual who not understand Malay and English * Individual who not understand instructions and obey commands * Individual who difficult to reach via telephone, email or social media

Design outcomes

Primary

MeasureTime frameDescription
Cardiovascular fitnessChange from baseline of cardiovascular endurance at 4 months6-Minute Wheelchair Push Test (6-MWPT)
Muscle strengthChange from baseline of upper limbs strength at 4 monthsThe upper limb strength measure by using BIODEX ® Isokinetic machine
Muscle strength normalize with body weightChange from baseline of upper limbs strength normalize body weight at 4 monthsThe upper limb strength normalize with body weight measure by using BIODEX ® Isokinetic machine
Muscle enduranceChange from baseline of upper limbs endurance at 4 monthsThe upper limb endurance measure by using BIODEX ® Isokinetic machine
Grip strengthChange from baseline of grip strength at 4 monthsThe JAMAR ® hand held dynamometer
Exercise self-efficacyChange from baseline of exercise self-efficacy at 4 monthsThe Spinal Cord Injury Exercise Self-Efficacy (ESES)
Physical activity levelChange from baseline of physical activity level at 4 monthsThe Physical Activity Scale for Individuals with Physical Disabilities (PASIPD)

Contacts

Primary ContactHafifi Hisham
hafifi.hisham@rehabmalaysia.com+6011-21215931
Backup ContactHaidzir Manaf
haidzir5894@puncakalam.uitm.edu.my+6012-6615246

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026