The primary goal of this research project is to develop and evaluate the effect of a 6-weeks cycling training program for adults with cerebral parese on the physical capacity, walking function, participation, and active lifestyle (part 2). An…
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Source
Brief title
Condition
- Pregnancy, labour, delivery and postpartum conditions
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main outcome measure is the physical capacity, measured as the peak power
output. The peak power output will be determined during a maximal exercise
protocol on a cycle ergometer.
Secondary outcome
Submaximal parameters (oxygen uptake, heart rate, mechanical efficiency)
Sprint power
Muscle strength lower extremities
Walking ability
Mass and height
Skinfold thickness
Active lifestyle, measured by a questionnaire (PASIPD)
Participation, measured by a questionnaire (SIP68)
Background summary
An inactive lifestyle and secondary problem often play a central role in daily
life of people with a disability. To prevent secondary complications and to
improve the physical capacity, it is important that people with a disability
participate in sport activities. However, it is difficult for them to join
regular sport clubs because specific knowledge and equipment is often not
available. For people with and without a disability, who participate in sport,
it is important that their performance (i.e. fitness, strenght, speed) is
tested regularly. With these test results the capacity of the persons can be
determined, which is necessay for developing a good individual training
protocol.
Very little information is available about test and training protocols for
adults with cerebral palsy. The purpose of this study is to develop knowledge
about the most ideal test and training protocol for adults with cerebral palsy.
With this knowledge we are better able to advise people with a cerebral palsy
who want to participate in recreational or elite sports.
Study objective
The primary goal of this research project is to develop and evaluate the effect
of a 6-weeks cycling training program for adults with cerebral parese on the
physical capacity, walking function, participation, and active lifestyle (part
2).
An associated goal is to develop and evaluate a reliable and valid test
protocol for aduls with cerebral palsy (part 1). The results of this test
protocol will be used to develop and evaluate the training program.
Study design
A controlled-randomized trial (part 2).
Intervention
The intervention is a 6-weeks cycling training program, 3x/week for 45 minutes
on 50% heart rate reserve on a cycle ergometer.
Study burden and risks
Part 1: Subjects will perform tests on 3 test days to determine the physical
capacity, walking function, active lifestyle and participation and their
relationship.
Part 2: Subjects will participate in a 18 weeks research project, executing a 6
week training program on a cycle ergometer, 3 days/week 45 min on 50% heart
rate reserve. Measurements will be performed at 3 different time slots.
Subjects 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 therapist and safety precautions
throughout training and testing. The expected benificial training effects in
combination with the limited risks would justify execution of the proposed
study.
Van der Boechorststraat 9
1081 BT Amsterdam
NL
Van der Boechorststraat 9
1081 BT Amsterdam
NL
Listed location countries
Age
Inclusion criteria
Diagnosis of Cerebral Palsy;
Stable medication use;
They have to be cognitively able to understand and perform the tasks;
Exclusion criteria
Medication use that affects muscle performance negatively;
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 lower extremities or back.
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
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL21815.029.08 |