The primary objective is to evaluate the effectiveness of low-intensity hand rim wheelchair exercise training on physical capacity, daily (wheelchair) functioning, participation and quality of life in people with a spinal cord injury. Furthermore,…
ID
Source
Brief title
Condition
- Spinal cord and nerve root disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameter is the physical capacity, measured by the peak power
output. The peak power output is assessed during a peak exercise test in a
wheelchair on a treadmill.
Secondary outcome
Secundary study parameters are: (sub)maximal capacity, propulsion technique,
pain and functioning of the upper extremities, respiratory function, muscle
strength, sprint capacity, wheelchair skills, independence (SCIM), metabolic
syndrome, participation, quality of life and personal- and environmental
factors.
Background summary
People with a spinal cord injury are often dependent on a (hand rim) wheelchair
and have an inactive lifestyle. Therefore, it is important to develop a good
protocol for wheelchair training, which prevents overuse of the musculoskeletal
system on one hand and improves the physical capacity and prevents the
occurrence of secondary complications on the other hand.
In the world of sport the training guidelines of the ACMS (ACSM, 1993, 1997)
are often used. An intensity of 70-80%HRR, a frequency of 3-5x/week and a
duration of 20-30 min. are in general accepted criteria to induce a training
effect.
However, Haskell (1994) proposed different training guidelines to improve
physical fitness and health. According to Haskell, exercise at a lower
intensity (30-40%HRR) and with a more divers pattern of light activities of
different durations performed every day (like activities of daily living),
might be more suitable for (extreme) inactive people. Additionally the risk for
overuse injuries will be smaller. In 2006 a research project has been performed
to study the effect of a 7-week low-intensity (30%HRR, 3x 70 min/week)
wheelchair training in able-bodied subjects. The results showed that a
low-intensity wheelchair training can improve the physical capacity and
propulsion technique in healty young men. The next step is to investigate the
effect of this training in inactive people with a chronic spinal cord injury.
Study objective
The primary objective is to evaluate the effectiveness of low-intensity hand
rim wheelchair exercise training on physical capacity, daily (wheelchair)
functioning, participation and quality of life in people with a spinal cord
injury. Furthermore, the effect on secondary complications such as upper body
overuse and cardiovascular risk factors in inactive people with a chronic
spinal cord injury will be studied.
Study design
A controlled randomized trial
Intervention
The experimental groups will receive 16-week low-intensity wheelchair exercise
training (35%HRR; 2x30min/week) or handcycling training (70%HRR, 2x30 min/week)
while the control group will not receive any training.
Study burden and risks
Subjects will participate in a 10-months research project executing a 16 week
wheelchair or handbike training-program on a treadmill, 2 days/week 30 min on
35%HRR (wheelchair) or 30 min on 70%HRR (handbike).
Measurements will be performed at 4 different time slots.
Subject may experience some discomfort and/or muscle soreness after the peak
exercise test or training. Furthermore, the risks during training and testing
sessions are relatively low because of thorough screening prior to
participation, use of skilled and licensed therapists and safety precautions
throughout training and testing. The expected beneficial training effects in
combination with the limited risks would justify execution of the proposed
study.
Antonius Deusinglaan 1
9713 AV Groningen
NL
Antonius Deusinglaan 1
9713 AV Groningen
NL
Listed location countries
Age
Inclusion criteria
Spinal cord injury
Wheelchair-dependent
28 - 65 years
Time since injury > 10y
Exclusion criteria
Cardiovascular contra-indications for testing according to the American College of Sports Medicine (ACSM) guidelines, or a resting diastolic blood pressure above 90 mm Hg or a resting systolic blood pressure above 180 mm Hg
Musculoskeletal complaints of the upper extremities, neck or back.
Progressive disease
Psychiatric problem
Not having enough knowledge of the Dutch language to understand the purpose of the study and the testing methods.
Plans to start another lifestyle (e.g. more physical active, diet) in the months that the experiment is going on.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
In other registers
Register | ID |
---|---|
CCMO | NL21812.029.08 |
OMON | NL-OMON27828 |