The objective of this study is determine the functional outcome in daily life of adults with obstetric brachial plexus injury and determine which limitations in daily life they encounter, functional as well as psychological and social.
ID
Source
Brief title
Condition
- Spinal cord and nerve root disorders
- Therapeutic procedures and supportive care NEC
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Action Research Arm test
RAND-36 (Dutch SF-36)
DUX-25 plexus
All related to original level of the injury
Secondary outcome
Correlations between strength and sensibility, strenght and function and
function and sensibility.
Number of "secundary" orthopedic interventions.
Background summary
There is no research on functional outcome in adults with obstetric brachial
plexus injury. Nowadays nerve reconstruction is a possible treatment.
Neurosurgeons are reconsidering the indication for this intervention because
operated patients often still need orthopaedic surgery at a later time. It is
not clear if this happens more often or not in patients who have not had nerve
reconstruction. To get a better idea we need information on a group of patients
with comparable injury who have not had nerve reconstruction.
A second concern is that not many adults with obstetric brachial plexus injury
consult the department of rehabilitation or the neurosurgeon concerned with
peripheral nerve injury. The patients who do report themselves often have
serious limitations in their daily activities and complaints of pain. Because
of their serious complaints it is imaginable that patients who don't report do
experience limitations en and pain in a lesser degree. It is possible that with
intervention in an earlier stage the complaints can be prevented or decreased.
Patients may be not aware of the possibilities of intervention.
Study objective
The objective of this study is determine the functional outcome in daily life
of adults with obstetric brachial plexus injury and determine which limitations
in daily life they encounter, functional as well as psychological and social.
Study design
Retrospective, observational study, without control group.
Study burden and risks
The participants are asked to visit the department of rehabilitation of the
LUMC. There they will be asked to fill out the questionnaires, a structured
physical examniation will be performed and the ARA test will be done.
It is estimated that all the tests will take 2 hours to complete.
There are no risks involved in this investigation.
The participants have no benefits in this investigation.
Albinusdreef 2
2333 ZA Leiden
Nederland
Albinusdreef 2
2333 ZA Leiden
Nederland
Listed location countries
Age
Inclusion criteria
adults
unilateral obstetric brachial plexus injury
Exclusion criteria
insufficient cognitive ability to fill out the questionnaires
progressive neurological disease such as Multiple Sclerosis
peripheral nerve disease such as polyneuropathy or carpal tunnel syndrome
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 | NL15177.058.06 |