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A randomised controlled trial of a specialised multidisciplinary consultation team to improve the outcomes of patients with recent onset spinal cord injury in acute hospital

A randomised controlled trial of a specialised multidisciplinary consultation team to improve the outcomes of patients with recent onset spinal cord injury in acute hospital

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000164099
Enrollment
72
Registered
2010-02-19
Start date
2010-09-30
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Patients with spinal cord injury (SCI) have improved outcomes with a specialized and systematic approach to their care. The management of nontraumatic SCI (NTSCI) is more fragmented compared with traumatic SCI (TSCI). Whereas patients with TSCI are often managed within specialised SCI units Patients with NTSCI can be admitted to a wide range of hospitals, receive care from many different hospital departments, and wait prolonged periods for a rehabilitation bed after they have been accepted as ready for transfer to rehabilitation. There is generally a lack of specialist SCI knowledge and related practical skill among acute hospital staff about the principles of caring for patients with a SCI. This places these patients at higher risk of preventable complications and adverse outcomes. This project is a study of the possible benefits of involving a specialized multidisciplinary consultation team of health care professionals in the management of patients with a recent onset of SCI who are in acute hospitals. The team will function as a mobile unit, assessing and providing therapy recommendations, simple equipment and limited treatment for SCI patients accepted by the Spinal Rehabilitation Unit (SRU) at Caulfield Hospital for admission to the unit and who are waiting for transfer. The median time for transfer is currently over 2 weeks. These patients tend to have a NTSCI. Patients accepted for admission to the SRU at Caulfield Hospital, Alfred Health, will be approached to participate in the study. Those who agree will be randomly allocated to receive either the multidisciplinary consultation team or usual care. It is our hypothesis that the team would significantly improve patient outcomes and prevent SCI complications.

Interventions

The intervention consists of a specialised multidisciplinary consultation team from the Spinal Rehabilitation Unit (SRU) at Caulfield Hospital (CH), Melbourne, Australia. The team will include a rehabilitation medicine doctor, physiotherapy and occupational therapy personnel with expertise in spinal cord injury (SCI) rehabilitation. The team will function as a mobile unit, assessing and reviewing SCI patients in acute hospitals. The physiotherapist and occupational therapist will see the pati

The intervention consists of a specialised multidisciplinary consultation team from the Spinal Rehabilitation Unit (SRU) at Caulfield Hospital (CH), Melbourne, Australia. The team will include a rehabilitation medicine doctor, physiotherapy and occupational therapy personnel with expertise in spinal cord injury (SCI) rehabilitation. The team will function as a mobile unit, assessing and reviewing SCI patients in acute hospitals. The physiotherapist and occupational therapist will see the patient for an initial focused assessment, jointly where practical. They will provide the patient and acute hospital treating team with patient-specific written and verbal advice, as relevant and appropriate, to optimise the patients’ care and outcomes. Self-care equipment and exercise equipment may also be provided to patients (with education on correct use) where indicated. The acute hospital nursing and allied health staff working with the patient will be engaged throughout the intervention process with the members of the specialised multidisciplinary consultation team. These efforts will be directed at trying to help improve patients’ independence and regain their ability to perform activities affected by their SCI, prevent SCI-related complications, and start specialist SCI rehabilitation strategies sooner than would otherwise be possible. It will be suggested that the recommendations made by the specialised multidisciplinary consultation team be incorporated into the patients existing program in the acute hospital. The patients’ status will be monitored and reviewed by a telephone call to the SCI patients treating acute hospital nursing or allied health team by at least one member of the specialised multidisciplinary consultation team within a week of initial assessment. All patients would have a direct medical review by one of the medical members of the team 7-10 days after the initial medical assessment and an allied health review (by either or both the physiotherapist and occupational therapist) within 7-10 days of the initial allied health review. Further direct reviews will occur 7-10 days after the second visit if clinically indicated and if the patient has not yet been admitted to the SRU. The duration of the intervention will be over the time after randomisation that the participant is in acute hospital, until admission to the SRU. It is not possible to state exactly what this duration will be, but it is anticipated that the expected duration will be about 1-6 weeks. For practical purposes, the study will limit inclusion to the 4 closest acute hospitals that refer the majority of SCI patients to the SRU at Caulfield Hospital, as listed above. The allied health members of the Consultation Team will all be qualified practitioners in their field and employed at Caulfield Hospital. Application for establishment of Honorary appointments will be made to the participating sites where consultation team members are not employed.

Sponsors

Dr Peter New
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Only patients with a recent onset SCI will be eligible for inclusion. The onset of the SCI could occur either as a result of illness or trauma that led to hospitalisation, or developed during a hospital admission of another condition. Patients with either non-traumatic spinal cord injury or traumatic spinal cord injury will be included.

Exclusion criteria

Patients will be excluded if either of the following apply, they: Have an established SCI that existed before presentation at hospital or Have an acquired brain injury, either pre-existing or related to their SCI, or other cognitive problems such as dementia that may impact upon their ability to learn complex information and provide informed consent. Are unable to provide informed consent and read the patient-specific information due to their level of English comprehension. Have an established pelvic region pressure ulcer at time of enrolment (as this will limit the ability of the patient to participate fully in the interventions offered by the team and assessed by the primary outcome measure) Have a complete tetraplegia at the eighth cervical spinal cord level or above

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026