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

U

Universiti Teknologi Mara

Status

Unknown

Conditions

Spinal Cord Injuries
Physical Disability

Treatments

Other: Conventional Physical Therapy
Other: Graded Exercise Integrated Education

Study type

Interventional

Funder types

Other

Identifiers

NCT03420170
Universiti Teknologi MARA

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Graded Exercise Integrated Education
Experimental group
Description:
The graded exercise (8 weeks) 1. Strengthening exercise 2. Aerobic Exercise Educational session to increase exercise self-efficacy and physical activity level (16 weeks)
Treatment:
Other: Graded Exercise Integrated Education
Conventional physical therapy
Active Comparator group
Description:
Normal routine of physical therapy (8 weeks)
Treatment:
Other: Conventional Physical Therapy

Trial contacts and locations

0

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Central trial contact

Haidzir Manaf; Hafifi Hisham

Data sourced from clinicaltrials.gov

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