The primary objective is to compare forces and moments acting on the shoulder of manual wheelchair users during power assisted wheelchair propulsion and manual wheelchair propulsion and the perceived upper extremity load. The secondary objectives…
ID
Source
Brief title
Condition
- Other condition
- Neuromuscular disorders
Synonym
Health condition
Manuele rolstoel gebruikers
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Main study parameter is shoulder load (perceived shoulder load and objectively
measured load).
Secondary outcome
Secondary study parameters are intensity, frequency and influence on daily
activities of shoulder pain; distance, velocity and time daily travelled;
wheelchair skills; energy expenditure; community participation, self-esteem and
user satisfaction.
Background summary
Manual wheelchair users rely extensively on their upper extremities for
mobility. Unfortunately, upper extremity complaints among wheelchair users are
a common problem. Work requirements of manual wheelchair propulsion that have
been linked to shoulder injuries are the repetitive (high) forces and moments
at the shoulder, extremes of motion during propulsion and muscular imbalance. A
power assisted wheelchair can be useful to decrease the workload, thereby
possibly reducing the risk on developing shoulder injuries. However, no
previous research has been published about the influence of power assisted
propulsion on forces and moments exerted on the rim and acting on the shoulder.
Therefore this is our primary goal. Because the force needed to propel the
wheelchair is partly delivered by a motor, we hypothesize that the forces and
moments exerted on the rim will decrease. Consequently, forces and moments at
the glenohumeral joint and muscle activation amplitude of push phase muscles
will decrease. Because, the transition to another type of wheelchair will
influence subjects in a broader perspective than only upper extremity function.
When a subject has less shoulder complaints or wheelchair propulsion costs less
energy, the activity level and participation in social activities can increase.
Because of this we will also investigate the differences on activity and
participation between manual and power assisted wheelchair propulsion.
Study objective
The primary objective is to compare forces and moments acting on the shoulder
of manual wheelchair users during power assisted wheelchair propulsion and
manual wheelchair propulsion and the perceived upper extremity load. The
secondary objectives are to assess the differences between power assisted
wheelchair propulsion and manual wheelchair propulsion on (a) the intensity and
frequency of shoulder pain, and the influence of shoulder pain on daily
activities, (b) activity during a day and wheelchair skills, (c) self efficacy
and user satisfaction.
Study design
This study is a longitudinal intervention study with a cross-over design.
Intervention
Power assisted wheels mounted on their own wheelchair frame.
Study burden and risks
Turns are easier in a power assisted wheelchair. By accidental means the
displacement of the wheelchair might be larger than expected, so people can
collide with obstacles in the environment. The power assist wheels are heavier
which might give problems in car transfers.
Roessinghsbleekweg 33b
7522 AH Enschede
NL
Roessinghsbleekweg 33b
7522 AH Enschede
NL
Listed location countries
Age
Inclusion criteria
• Manual wheelchair user for at least one year due to a neurological disorder.
• The subjects should be able to propel a manual wheelchair bimanually.
• Medically and physically stable, judged by subjects own rehabilitation physician.
• Sufficient trunk stability to maintain posture.
• Age 18 or older.
• Subjects should be able to use their usual mode of transportation with the power assisted wheels.
• The power assist wheels should fit on the subjects own wheelchair frame.
Exclusion criteria
- Use of any type of PAPAW.
- Extreme shoulder pain, contractures upper extremity and/or spasticity which made manual wheelchair propulsion for the duration of the measurements impossible.
- Cognitive or communicative impairments which made cooperation with the study protocol compromised.
Design
Recruitment
Medical products/devices used
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In other registers
Register | ID |
---|---|
CCMO | NL35398.044.11 |