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Fitness Training After Traumatic Brain Injury

The Efficacy of a Supervised Fitness Centre-Based Exercise Programme Compared to an Unsupervised Home-Based Exercise Programme on Improving Fitness and Psychosocial Outcomes in a Traumatic Brain Injured Population

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00251108
Enrollment
60
Registered
2005-11-09
Start date
2003-10-31
Completion date
2007-03-31
Last updated
2007-03-01

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

Conditions

Craniocerebral Trauma

Keywords

'traumatic brain injury', 'head injury', 'brain injuries', 'exercise therapy', 'physical fitness'

Brief summary

The aim of this project is to compare the efficacy of two different fitness exercise programmes on improving fitness and psychosocial functioning in a traumatic brain injured population. We hypothesize that a supervised fitness-centre based exercise programme, compared to an unsupervised home-based exercise programme will show significant improvements in cardiorespiratory fitness, depression and community integration.

Detailed description

The objective of this project is to compare a three-month supervised fitness centre-based exercise programme to a 3-month unsupervised home-based exercise programme on discharge from inpatient rehabilitation on improving cardiorespiratory fitness and psychosocial functioning in a traumatic brain injured population. We plan to carry out a multi-centre, assessor blinded, randomised controlled trial with a parallel group design to compare the two interventions. We hypothesise that the supervised fitness-centre based programme will provide significantly better outcomes, and that these gains will not only be evident on completion of the programme, but will be maintained on follow-up, thereby demonstrating that investment in a supervised exercise programme can provide beneficial long-term effects.

Interventions

Sponsors

Motor Accidents Authority of NSW
CollaboratorUNKNOWN
Sydney South West Area Health Service
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
15 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patients who have sustained a traumatic brain injury who have completed their inpatient rehabilitation at either of the three Sydney Metropolitan Brain Injury Units (Liverpool, Ryde or Westmead) will be included in this study if they: * have sustained a very severe or extremely severe traumatic brain injury * have had a hospital admission of \> 1 month * are able to walk independently at \> 1 m/s on discharge * are able to commit 3 hours per week to a fitness programme * live within the area serviced by the 3 units

Exclusion criteria

* have a concurrent medical condition for which moderate to high intensity exercise is contraindicated * are still in Posttraumatic Amnesia (PTA) * have cognitive or language problems that affect their ability to understand verbal instructions * have behaviour problems not suitable for a fitness centre environment

Design outcomes

Primary

MeasureTime frame
Measure of Cardiorespiratory fitness:Modified 20 metre Walk/Run Shuttle Test:

Secondary

MeasureTime frame
Profile of Moods Scale (POMS)
BICRO-39
Sydney Psychosocial Reintegration Scale (SPRS)
Depression Anxiety Stress Scales (DASS)
Rate of Perceived Exertion (RPE)
Hip to Waist ratio
Body Mass Index (BMI)

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026